| Drug Recalls

Zactos

dom — Sat, 26 Nov 2011 15:38:00 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ZACTOS, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

It can be very frightening to find out that the drug you have been taking may have been recalled, or may be the subject of government warnings due to its dangerous side effects. If the drug you have been taking has caused you serious harm, consult with medical professionals immediately. Then, to determine if you qualify to bring a legal claim for financial compensation for your injuries, contact us for a free case evaluation.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Zactos, also known as Actos, Glustin, Pioglitazone, Pioz and Glizone, is a drug used for the treatment of diabetes and hyperglycemia. In 2008, the drug came in at number 10 in the United States for the year’s best selling drugs with sales of just over $2.4 billion. The drug has been available since 1999 and is made by Takeda Pharmaceuticals.

Zactos works in reducing the liver’s insulin resistance, decreases glucose withdrawal in the liver, increases insulin-dependent glucose expense and reduces insulin, glycated hemoglobin and glucose in the patient’s bloodstream. In addition, it has been shown to assist in the reduction of triglyceride levels and increases HDLs without causing a change in LDLs or total cholesterol. Although the drug’s main purpose is to treat type 2 diabetes mellitus, it is has also been used to treat fatty liver disease and has been shown to decrease diabetes risk in those diagnosed with prediabetes or borderline diabetes.

Zactos is contraindicated in patients with pioglitazone hypersensitivity, as well as those with sensitivity to thiazolidinediones and any forms of them. It is also contraindicated in the treatment of type 1 diabetes mellitus and could actually be harmful if used in these patients. It has not been established whether or not the drug is safe for pregnant or breastfeeding mothers or for those under the age of 18. In addition, the drug is not recommended for anyone suffering from liver disease of any type or in patients suffering from heart failure.

Side Effects of Zactos

The side effects of Zactos vary in nature from the mild and more common to those side effects that are more severe in nature and occur rarely. A brief listing of the side effects of Zactos is listed below:

• Anemia
• Congestive heart failure
• Fluid retention
• Headache
• Hypoglycemia
• Upper arm, foot and hand fractures
• Peripheral edema
• Weight gain
• Tooth problems
• Sinusitis
• Myalgia
• Upper respiratory tract infection
• Myocardial ischemic events
• Increased risk of bladder cancer

The FDA has forced the manufacturer of Zactos to add a black box warning regarding the drug’s extremely dangerous side effects, namely the potential for heart failure and bladder cancer. This warning is the FDA’s most strict and is the highest step that can be taken other than removing a drug from the market completely.

These more extreme risks have been shown in study date to be increased in patients that use Zactos for extended periods of time. However, the drug’s manufacturer is busy conducting additional tests to further determine the risks of the drug. Further studies have shown that a patient’s risk increases with the dosage of Zactos as well as the treatment duration. The review of the five year study showed that patients using the drug for more than a year had an increased bladder cancer risk, which is ultimately what influenced the FDA to place the warning. However, the manufacturer is conducting a more comprehensive 10-year study to obtain additional information regarding the true risks.

Glizone

dom — Sat, 26 Nov 2011 15:34:21 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY GLIZONE, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Glizone, also known as Actos, Glustin, Pioglitazone, Pioz and Zactos, is a drug used for the treatment of diabetes and hyperglycemia. In 2008, the drug came in at number 10 in the United States for the year’s best selling drugs with sales of just over $2.4 billion. The drug has been available since 1999 and is made by Takeda Pharmaceuticals.

Glizone works in reducing the liver’s insulin resistance, decreases glucose withdrawal in the liver, increases insulin-dependent glucose expense and reduces insulin, glycated hemoglobin and glucose in the patient’s bloodstream. In addition, it has been shown to assist in the reduction of triglyceride levels and increases HDLs without causing a change in LDLs or total cholesterol. Although the drug’s main purpose is to treat type 2 diabetes mellitus, it is has also been used to treat fatty liver disease and has been shown to decrease diabetes risk in those diagnosed with prediabetes or borderline diabetes.

Glizone is contraindicated in patients with pioglitazone hypersensitivity, as well as those with sensitivity to thiazolidinediones and any forms of them. It is also contraindicated in the treatment of type 1 diabetes mellitus and could actually be harmful if used in these patients. It has not been established whether or not the drug is safe for pregnant or breastfeeding mothers or for those under the age of 18. In addition, the drug is not recommended for anyone suffering from liver disease of any type or in patients suffering from heart failure.

Side Effects of Glizone

The side effects of Glizone vary in nature from the mild and more common to those side effects that are more severe in nature and occur rarely. A brief listing of the side effects of Glizone is listed below:

The FDA has forced the manufacturer of Glizone to add a black box warning regarding the drug’s extremely dangerous side effects, namely the potential for heart failure and bladder cancer. This warning is the FDA’s most strict and is the highest step that can be taken other than removing a drug from the market completely.

These more extreme risks have been shown in study date to be increased in patients that use Glizone for extended periods of time. However, the drug’s manufacturer is busy conducting additional tests to further determine the risks of the drug. Further studies have shown that a patient’s risk increases with the dosage of Glizone as well as the treatment duration. The review of the five year study showed that patients using the drug for more than a year had an increased bladder cancer risk, which is ultimately what influenced the FDA to place the warning. However, the manufacturer is conducting a more comprehensive 10-year study to obtain additional information regarding the true risks.

Pioz

dom — Sat, 26 Nov 2011 15:28:49 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY PIOZ, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Pioz, also known as Actos, Glustin, Pioglitazone, Glizone and Zactos, is a drug used for the treatment of diabetes and hyperglycemia. In 2008, the drug came in at number 10 in the United States for the year’s best selling drugs with sales of just over $2.4 billion. The drug has been available since 1999 and is made by Takeda Pharmaceuticals.

Pioz works in reducing the liver’s insulin resistance, decreases glucose withdrawal in the liver, increases insulin-dependent glucose expense and reduces insulin, glycated hemoglobin and glucose in the patient’s bloodstream. In addition, it has been shown to assist in the reduction of triglyceride levels and increases HDLs without causing a change in LDLs or total cholesterol. Although the drug’s main purpose is to treat type 2 diabetes mellitus, it is has also been used to treat fatty liver disease and has been shown to decrease diabetes risk in those diagnosed with prediabetes or borderline diabetes.

Pioz is contraindicated in patients with pioglitazone hypersensitivity, as well as those with sensitivity to thiazolidinediones and any forms of them. It is also contraindicated in the treatment of type 1 diabetes mellitus and could actually be harmful if used in these patients. It has not been established whether or not the drug is safe for pregnant or breastfeeding mothers or for those under the age of 18. In addition, the drug is not recommended for anyone suffering from liver disease of any type or in patients suffering from heart failure.

Side Effects of Pioz

The side effects of Pioz vary in nature from the mild and more common to those side effects that are more severe in nature and occur rarely. A brief listing of the side effects of Pioz is listed below:

The FDA has forced the manufacturer of Pioz to add a black box warning regarding the drug’s extremely dangerous side effects, namely the potential for heart failure and bladder cancer. This warning is the FDA’s most strict and is the highest step that can be taken other than removing a drug from the market completely.

These more extreme risks have been shown in study date to be increased in patients that use Pioz for extended periods of time. However, the drug’s manufacturer is busy conducting additional tests to further determine the risks of the drug. Further studies have shown that a patient’s risk increases with the dosage of Pioz as well as the treatment duration. The review of the five year study showed that patients using the drug for more than a year had an increased bladder cancer risk, which is ultimately what influenced the FDA to place the warning. However, the manufacturer is conducting a more comprehensive 10-year study to obtain additional information regarding the true risks.

Pioglitazone

dom — Sat, 26 Nov 2011 15:22:41 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY PIOGLITAZONE, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Pioglitazone, also known as Actos, Glustin, Pioz, Glizone and Zactos, is a drug used for the treatment of diabetes and hyperglycemia. In 2008, the drug came in at number 10 in the United States for the year’s best selling drugs with sales of just over $2.4 billion. The drug has been available since 1999 and is made by Takeda Pharmaceuticals.

Pioglitazone works in reducing the liver’s insulin resistance, decreases glucose withdrawal in the liver, increases insulin-dependent glucose expense and reduces insulin, glycated hemoglobin and glucose in the patient’s bloodstream. In addition, it has been shown to assist in the reduction of triglyceride levels and increases HDLs without causing a change in LDLs or total cholesterol. Although the drug’s main purpose is to treat type 2 diabetes mellitus, it is has also been used to treat fatty liver disease and has been shown to decrease diabetes risk in those diagnosed with prediabetes or borderline diabetes.

Pioglitazone is contraindicated in patients with pioglitazone hypersensitivity, as well as those with sensitivity to thiazolidinediones and any forms of them. It is also contraindicated in the treatment of type 1 diabetes mellitus and could actually be harmful if used in these patients. It has not been established whether or not the drug is safe for pregnant or breastfeeding mothers or for those under the age of 18. In addition, the drug is not recommended for anyone suffering from liver disease of any type or in patients suffering from heart failure.

Side Effects of Pioglitazone

The side effects of Pioglitazone vary in nature from the mild and more common to those side effects that are more severe in nature and occur rarely. A brief listing of the side effects of Pioglitazone is listed below:

The FDA has forced the manufacturer of Pioglitazone to add a black box warning regarding the drug’s extremely dangerous side effects, namely the potential for heart failure and bladder cancer. This warning is the FDA’s most strict and is the highest step that can be taken other than removing a drug from the market completely.

These more extreme risks have been shown in study date to be increased in patients that use Pioglitazone for extended periods of time. However, the drug’s manufacturer is busy conducting additional tests to further determine the risks of the drug. Further studies have shown that a patient’s risk increases with the dosage of Pioglitazone as well as the treatment duration. The review of the five year study showed that patients using the drug for more than a year had an increased bladder cancer risk, which is ultimately what influenced the FDA to place the warning. However, the manufacturer is conducting a more comprehensive 10-year study to obtain additional information regarding the true risks.

Glustin

dom — Sat, 26 Nov 2011 15:16:57 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY GLUSTIN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Glustin, also known as Actos, Pioglitazone, Pioz, Glizone and Zactos, is a drug used for the treatment of diabetes and hyperglycemia. In 2008, the drug came in at number 10 in the United States for the year’s best selling drugs with sales of just over $2.4 billion. The drug has been available since 1999 and is made by Takeda Pharmaceuticals.

Glustin works in reducing the liver’s insulin resistance, decreases glucose withdrawal in the liver, increases insulin-dependent glucose expense and reduces insulin, glycated hemoglobin and glucose in the patient’s bloodstream. In addition, it has been shown to assist in the reduction of triglyceride levels and increases HDLs without causing a change in LDLs or total cholesterol. Although the drug’s main purpose is to treat type 2 diabetes mellitus, it is has also been used to treat fatty liver disease and has been shown to decrease diabetes risk in those diagnosed with prediabetes or borderline diabetes.

Glustin is contraindicated in patients with pioglitazone hypersensitivity, as well as those with sensitivity to thiazolidinediones and any forms of them. It is also contraindicated in the treatment of type 1 diabetes mellitus and could actually be harmful if used in these patients. It has not been established whether or not the drug is safe for pregnant or breastfeeding mothers or for those under the age of 18. In addition, the drug is not recommended for anyone suffering from liver disease of any type or in patients suffering from heart failure.

Side Effects of Glustin

The side effects of Glustin vary in nature from the mild and more common to those side effects that are more severe in nature and occur rarely. A brief listing of the side effects of Actos is listed below:

The FDA has forced the manufacturer of Glustin to add a black box warning regarding the drug’s extremely dangerous side effects, namely the potential for heart failure and bladder cancer. This warning is the FDA’s most strict and is the highest step that can be taken other than removing a drug from the market completely.

These more extreme risks have been shown in study date to be increased in patients that use Glustin for extended periods of time. However, the drug’s manufacturer is busy conducting additional tests to further determine the risks of the drug. Further studies have shown that a patient’s risk increases with the dosage of Glustin as well as the treatment duration. The review of the five year study showed that patients using the drug for more than a year had an increased bladder cancer risk, which is ultimately what influenced the FDA to place the warning. However, the manufacturer is conducting a more comprehensive 10-year study to obtain additional information regarding the true risks.

Actos

dom — Sat, 26 Nov 2011 15:02:28 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ACTOS, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Actos, also known as Glustin, Pioglitazone, Pioz, Glizone and Zactos, is a drug used for the treatment of diabetes and hyperglycemia. In 2008, the drug came in at number 10 in the United States for the year’s best selling drugs with sales of just over $2.4 billion. The drug has been available since 1999 and is made by Takeda Pharmaceuticals.

Actos works in reducing the liver’s insulin resistance, decreases glucose withdrawal in the liver, increases insulin-dependent glucose expense and reduces insulin, glycated hemoglobin and glucose in the patient’s bloodstream. In addition, it has been shown to assist in the reduction of triglyceride levels and increases HDLs without causing a change in LDLs or total cholesterol. Although the drug’s main purpose is to treat type 2 diabetes mellitus, it is has also been used to treat fatty liver disease and has been shown to decrease diabetes risk in those diagnosed with prediabetes or borderline diabetes.

Actos is contraindicated in patients with pioglitazone hypersensitivity, as well as those with sensitivity to thiazolidinediones and any forms of them. It is also contraindicated in the treatment of type 1 diabetes mellitus and could actually be harmful if used in these patients. It has not been established whether or not the drug is safe for pregnant or breastfeeding mothers or for those under the age of 18. In addition, the drug is not recommended for anyone suffering from liver disease of any type or in patients suffering from heart failure.

Side Effects of Actos

The side effects of Actos vary in nature from the mild and more common to those side effects that are more severe in nature and occur rarely. A brief listing of the side effects of Actos is listed below:

The FDA has forced the manufacturer of Actos to add a black box warning regarding the drug’s extremely dangerous side effects, namely the potential for heart failure and bladder cancer. This warning is the FDA’s most strict and is the highest step that can be taken other than removing a drug from the market completely.

These more extreme risks have been shown in study date to be increased in patients that use Actos for extended periods of time. However, the drug’s manufacturer is busy conducting additional tests to further determine the risks of the drug. Further studies have shown that a patient’s risk increases with the dosage of Actos as well as the treatment duration. The review of the five year study showed that patients using the drug for more than a year had an increased bladder cancer risk, which is ultimately what influenced the FDA to place the warning. However, the manufacturer is conducting a more comprehensive 10-year study to obtain additional information regarding the true risks.

Pramin

dom — Sun, 30 Oct 2011 02:38:42 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY PRAMIN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Pramin, also known as Metoclopramide, is what is known as a gastroprokinetic agent and antiemetic. The drug is frequently used in the treatment of vomiting or nausea and is often prescribed for patients suffering from gastroparesis to assist with gastric emptying. It has also been used to treat migraines.

If you have been a victim of Pramin and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Pramin has been given to treat the nausea and subsequent vomiting that is associated with morphine use, uremia, malignancy, infection, labor, migraines and radiation sickness. It has also been used in combination with acetaminophen or aspirin. Unfortunately, Pramin has proved to be ineffective in relieving nausea due to motion sickness, chemotherapy and postoperative nausea.

Pramin has also been used to inhibit dopamine’s action and stimulate lactation in mothers that are having trouble producing a suitable amount of milk for their breastfeeding infant.

Adverse Effects of Pramin

Women in every stage of pregnancy have used Pramin without issue to the unborn child or mother. The drug is excreted in the mother’s milk. However, Pramin does have several adverse effects associated with its use, most of which occur after long-term use. Some of the more common side effects are listed below:

· Constipation
· Depression
· Dizziness
· Drowsiness
· Extrapyramidal effects
· Headache
· Hyperprolactinaemia
· Hypertension
· Hypotension
· Focal dystonia
· Lassitude
· Oculogyric crisis
· Restlessness

Pramin has also been associated with some more serious side effects, including:

· Agranulocytosis
· Akathisia
· Aldosteronism (can be fatal)
· Depression/suicidal thoughts
· Jaundice
· Hallucinations
· Hyperaldosteronism
· Neuroleptic malignant syndrome
· Severe allergic reactions
· Seizures
· Supraventricular tachycardia
· Tardive dyskinesia

Any individual developing any of these serious complications while taking Pramin should immediately seek medical care and be sure to complete any prescribed treatments in order to achieve the best chance possible of recovery. Unfortunately, some of the more serious side effects of Pramin can be chronic and permanent, resulting in many previous Pramin users choosing to file suit against the manufacturer.

The FDA suggests that drugs like Pramin or Reglan only be used as a short term option, preferably under 12 weeks. This is due to the reports that tardive dyskinesia frequently occurs in patients using the drug in excess of three months. This same concern eventually influenced the FDA to require that all metoclopramide manufacturers issue black box warnings for the side effect tardive dyskinesia, noting that this occurs with high dosage or chronic use.

Pramin should not be taken in cases of phaeochromocytoma or a bowel obstruction. In addition, in patients with Parkinson’s disease it should be avoided or used cautiously. The same is true for those suffering from clinical depression because the drug can actually worsen the patient’s mental state with long-term use.

The drug Reglan is produced by pharmaceutical manufacturer Schwarz Pharma; however, it is known generically as metoclopramide and has been sold under several different brand names. These include: Degan, which is made by the manufacturer Lek; Primperan and Maxeran, both made by pharmaceutical company Sanofi Aventis; Maxolon, made by manufacturer Shire/Valeant; and Pylomid, made by a company called Bosnalijek.

If you have suffered a serious injury by taking Pramin, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Claravis®

dom — Sun, 30 Oct 2011 02:16:03 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY CLARAVIS, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Claravis is a drug that is used for treating severe cases of acne. The drug is also known as isotretinoin and has also been used to treat other skin conditions and cancers over the years. Initially, this drug was developed for chemo therapies to help with treating brain cancer as well as pancreatic cancer. It is still being used for these conditions as it has been shown to help kill off the cells that divide rapidly. It can additionally be used for treating ichthyosis, which happens is a form of a skin deformation.

Millions of individuals have taken this medication over the years. It is a drug that fights acne by eliminating the oil on the skin that gets released through the body’s oil glands. This helps the skin renew itself faster. There are, however, several side effects that have been found in individuals taking Claravis.

Side Effects of Claravis

The medication has created a lot of controversy over the years and so have its side effects. There are birth defects that come from pregnant women taking this medication as well as suicidal thoughts and depression. Additionally, there are intestinal disorders that may come with taking Claravis.

The most recent side effect that has been reported is bowel disease. This disease is accompanied by painful swelling of the intestines. There are two forms of this type of disease, which include Crohn’s disease as well as ulcerative colitis. Crohn’s disease is going to have the most effect on your small intestines. The most common side effects of bowel disease include:

Fever
Severe cramping and pain
Bloody diarrhea
Urgency to use the bathroom a lot
Severe flares of acne
Eye irritation
Thinning of hair
Back pain
Nose bleeds
Cataracts (rare)
Increase in liver enzymes
Weight loss that is unexplained as well as a decrease in appetite

Both of these disorders can result in fatal complications of your intestines. Some of these complications include your bowel rupturing, toxic megacolon, bleeding ulcers, and perineal disease and even colon cancer.

There is scientific data that has shown there are higher risks of birth defects if Claravis is taken during pregnancy. Women who are at their reproductive age may be recommended to stay away from this medication and any other forms of isotretinoin medications.

Women who are taking this medication are required to take two birth control pills and avoid from getting pregnant within at least one full month after ending this medication. There is an increased risk of miscarriages when taking this drug. Another significant side effect stems from risks of severe mental problems including depression, psychosis and even suicide. Hallucinations are also common while taking Accutane.

If you have experienced serious side effects as a result of taking Claravis/Rosiglitazone, a lawyer with experience in the ongoing Rosiglitazone litigation can help evaluate your claim at no charge. The Claravis recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Ectiva®

dom — Fri, 23 Sep 2011 15:52:20 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ECTIVA, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Ectiva, also known as Sibutramine, Reductil and Subutrex, was a drug used in the treatment of obesity up until 2010. Knoll Pharmaceuticals originally developed the drug, but Abbott Laboratories is the drug’s most recent manufacturer. The United States classifies the drug as a Schedule IV controlled substance. Meridia is a serotonin-norepinephrine reuptake inhibitor that acts centrally. The drug is related structurally to amphetamines, but it has a more distinct mechanism of action.

Although Ectiva is absorbed well in the GI tract, its bio-availability is reduced due to it undergoing first-pass metabolism. It typically reaches its peak at one hour and has a one hour half-life. The drug causes a re-uptake reduction of dopamine, serotonin and norepinephrine, which help to enhance satiety. The drug was approved in November of 1997 by the United States FDA to be used in obesity treatment. It is typically prescribed at a dosage of 10 mg to be taken once daily, but dosage can be increased after four weeks to 15 mg per day.

Ectiva, like many pharmaceuticals, has several contraindications. Patients and physicians should be aware that Ectiva should not be used or used with extreme caution in the following situations:

* Patients suffering from anorexia, bulimia, mania or depression, or in patients who have a history of alcohol abuse.

* Any patients under the age of 18, over age 65 or who display hypersensitivity to Meridia or its ingredients should not be prescribed this drug.

* Patients taking MAOIs, other centrally active medications or antidepressants should avoid Meridia.

* Patients with a history of uncontrolled hypertension, pulmonary hypertension, peripheral arterial disease, heart valve damage, those having had a myocardial infarction, coronary heart disease, serious arrhythmias, congestive heart failure, angina, tachycardia, stroke, peripheral arterial occlusive disease, transient ischemic attack, glaucoma, pheochromocytoma, hyperthyroidism, prostate enlargement or seizure disorders.

* Lactating or pregnant women

Side Effects of Ectiva

Like many helpful pharmaceuticals, Ectiva does have side effects associated with its use. These can range from the mild and common to the median and even more severe and rare reactions. A brief listing of the possible common side effects includes:

Constipation
Dizziness
Drowsiness
Dry mouth
Flushing
Headache
Increase in appetite
Joint or muscle pain
Menstrual cramps/increased pain
Nausea
Strange taste
Stomach queasiness/upset
Trouble sleeping

More serious side effects include:

Increased blood pressure
Stroke
Heart attack
Cardiac arrhythmias
Mood changes/changes in mental state
Paresthesia
Seizures
Abnormal bleeding or bruising
Chest pain
Jaundice
Edema
Dyspnea
Fever
Melena
Hematemesis
Hemiplegia
Rigors

Ectiva does have several clinical interactions. For instance, patients using Ectiva while taking MAOIs may increase the patient’s risk for serotonin syndrome. Ectiva should not be used within 14 days of starting or stopping the use of an MAOI. Serotonin syndrome risk may increase with the use of triptans, opiods, ergolines and migraine treatment drugs. However, Ectiva doesn’t seem to affect hormonal contraception.

If you have experienced serious side effects as a result of taking the drug Ectiva, a lawyer with experience in the ongoing Ectiva litigation can help evaluate your claim at no charge. The Ectiva recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Meridia®

dom — Fri, 23 Sep 2011 15:44:13 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY MERIDIA, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Meridia, also known as Sibutramine, Reductil and Subutrex, was a drug used in the treatment of obesity up until 2010. Knoll Pharmaceuticals originally developed the drug, but Abbott Laboratories is the drug’s most recent manufacturer. The United States classifies the drug as a Schedule IV controlled substance. Meridia is a serotonin-norepinephrine reuptake inhibitor that acts centrally. The drug is related structurally to amphetamines, but it has a more distinct mechanism of action.

Although Meridia is absorbed well in the GI tract, its bio-availability is reduced due to it undergoing first-pass metabolism. It typically reaches its peak at one hour and has a one hour half-life. The drug causes a re-uptake reduction of dopamine, serotonin and norepinephrine, which help to enhance satiety. The drug was approved in November of 1997 by the United States FDA to be used in obesity treatment. It is typically prescribed at a dosage of 10 mg to be taken once daily, but dosage can be increased after four weeks to 15 mg per day.

Meridia, like many pharmaceuticals, has several contraindications. Patients and physicians should be aware that Meridia should not be used or used with extreme caution in the following situations:

* Patients suffering from anorexia, bulimia, mania or depression, or in patients who have a history of alcohol abuse.

* Any patients under the age of 18, over age 65 or who display hypersensitivity to Meridia or its ingredients should not be prescribed this drug.

* Patients taking MAOIs, other centrally active medications or antidepressants should avoid Meridia.

* Lactating or pregnant women

Side Effects of Meridia

Like many helpful pharmaceuticals, Meridia does have side effects associated with its use. These can range from the mild and common to the median and even more severe and rare reactions. A brief listing of the possible common side effects includes:

Constipation
Dizziness
Drowsiness
Dry mouth
Flushing
Headache
Increase in appetite
Joint or muscle pain
Menstrual cramps/increased pain
Nausea
Strange taste
Stomach queasiness/upset
Trouble sleeping

More serious side effects include:

Meridia does have several clinical interactions. For instance, patients using Meridia while taking MAOIs may increase the patient’s risk for serotonin syndrome. Meridia should not be used within 14 days of starting or stopping the use of an MAOI. Serotonin syndrome risk may increase with the use of triptans, opiods, ergolines and migraine treatment drugs. However, Meridia doesn’t seem to affect hormonal contraception.

If you have experienced serious side effects as a result of taking the drug Meridia, a lawyer with experience in the ongoing Meridia litigation can help evaluate your claim at no charge. The Meridia recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Jensen Farms Cantaloupe Recall

dom — Fri, 23 Sep 2011 15:04:58 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY THE JENSEN FARMS CANTALOUPE RECALL, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Cantaloupe is an extremely popular fruit for breakfast, snacks, parties and more. Related to the pumpkin, cucumber, gourd and squash, it is a hardy netted melon fruit that has been traced as far back as 1700 A.D. Millions love cantaloupe for its deliciously sweet smell, the low calories per serving and its tantalizingly refreshing flavor. However, cantaloupe is also rich in vitamins A, B3, B6, folate, potassium and dietary fiber, making it a healthy accompaniment to any meal.

Cantaloupe grows on a somewhat aggressive, ground bound, trailing vine. The fruits are generally found in abundance in the months of June through the middle of September when cantaloupe tends to be at its best. However, as the summer of 2011 came to an end, this popular fruit was found to be responsible for causing an untold number of issues. A deadly listeria outbreak involving cantaloupes was discovered. Obviously, this has left countless people worried about consuming one of their favorite fruits, but many others have experienced something much worse than worry.

This listeria outbreak has been traced back to the Jensen Farms Rocky Ford cantaloupe crop. The outbreak has reportedly affected a minimum of 35 people throughout 10 states, two of which have died as a result. There is no speculation as to how many more individuals might have been affected by the outbreak, as it was first discovered in the first weeks of September 2011 and additional reports continue to come in. The CDC and officials of public health are continuing to research the outbreak to determine if the Rocky Ford cantaloupes from Jensen Farms are the only fruits involved in these cases.

Listeriosis is primarily caused by consuming foods that have been contaminated with listeria monocytogenes. The result is a very serious infection that can be deadly. The first lawsuit regarding the listeria outbreak has been filed by Marler Clark, a law firm representing a man from Colorado Springs who is still hospitalized due to the outbreak. The suit was filed on the 15th of September, 2011.

Symptoms of Listeria

Those who may have purchased and subsequently consumed a Rocky Ford cantaloupe that came from Jensen Farms should be aware of the symptoms of listeria and should seek immediate medical attention should they begin to experience any such symptoms. These symptoms include:

Aching muscles
Diarrhea
Fever
Nausea
Meningitis
Brain infection
Still birth or miscarriage in pregnant women

On the 14th of September, 2011, Jensen Farms announced a recall of its Rocky Ford cantaloupes. These cantaloupes are easily identifiable, as they include one of two stickers:

Green, yellow and gray sticker reading: Jensen Farms – Sweet Rocky Fords
White and green sticker reading: Product of USA – Frontera Produce – Colorado Fresh – Rocky Ford – Cantaloupe

The states that these cantaloupes had been distributed to include the following:

Arizona
Colorado
Illinois
Kansas
Minnesota
Missouri
Nebraska
New Jersey
New Mexico
New York
North Carolina
Oklahoma
Pennsylvania
Tennessee
Texas
Utah
Wyoming

If you believe that you or a family member has experienced any of the symptoms of listeria, seek medical attention immediately.

If you have experienced serious side effects as a result of consuming Jensen Farms Cantaloupe, a lawyer with experience in the ongoing Jensen Farms litigation can help evaluate your claim at no charge. The Jensen Farms recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Alendronic Acid

dom — Fri, 23 Sep 2011 14:26:48 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ALENDRONIC ACID, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Alendronic Acid also known as alendronate sodium, is a drug manufactured by Merck to be used in the treatment of osteoporosis, along with several other types of bone disease. It is a bisphosphonate that Merck held the patent on until 2008, when the company lost the many appeals filed in an effort to block others from creating an FDA approved generic version of Alendronic Acid.

Alendronic Acid is mainly used in the treatment of osteoporosis in females; however, it can also be used to treat osteoporosis in males. It has also been used in conjunction with vitamin D and calcium for the treatment and prevention of osteoporosis that is corticosteroid-related. In addition, it has also proven to be somewhat effective in the treatment of Paget’s disease.

Clinical data has shown that the bone turnover rate has been normalized with the use of Alendronic Acid in post-menopausal women, resulting in increased bone density in the hip, spine, wrist and overall body. Data shows that Alendronic Acid has actually decreased the fracture risk in women who were in the highest risk bracket by 50% on average.

Alendronic Acid has been contraindicated in several instances, such as in clinical manifestations of osteomalacia, hypocalcemia, those with an alendronate hypersensitivity issue, women that are breastfeeding or pregnant and patients that are unable to walk, sit or stand after 30 minutes following oral administration. In addition, patients with esophagitis, gastric ulserations or gastritis, renal impairment, strictures or achalasia and any patients under age 18 are cautioned against the use of this medication.

Side Effects of Alendronic Acid

Alendronic Acid has several side effects associated with its use. The most common of these side effects are:

Back pain
Bloating
Changes in taste
Constipation
Diarrhea
Dizziness
Full feeling
Flu-like symptoms
Gas
Headache
Joint pain
Muscle pain
Nausea
Vomiting

The more serious side effects of Alendronic Acid is what physicians and patients alike should be most concerned with. The more severe of Alendronic Acid’s side effects include:

Black, bloody or tarry stools
Chest pain
Coughing up blood or bloody vomit
Allergic reactions – difficulty breathing, hives, itching, rash, swelling in the face, lips, mouth, throat and tongue
Constant heartburn
Blistered, red, peeling or swollen skin
Bone, joint or muscle pain
Constant stomach pain or sore throat
Swelling in the joints, hands, legs or jaw
Spasms, muscle cramps, twitches, tingling or numbness around the mouth or in fingers and toes
Esophageal, gastric or duodenal ulceration.
Toxic epidermal necrolysis
Stevens-Johnson syndrome
Osteonecrosis of the Jaw
Low-impact femoral fractures

If patients consume milk, supplements or other drugs that contain large amounts of calcium, aluminum or magnesium, Alendronic Acid resorption is decreased. HRT has not been proven to cause any drug-drug interactions, nor have any been noted with fluorides or D analogues, although concomitant treatment should be avoided. In addition, NSAIDs combined with Alendronic Acid may actually elevate the risk for gastric ulcers.

If you have experienced serious side effects as a result of taking Alendronic Acid, a lawyer with experience in the ongoing Alendronic Acid litigation can help evaluate your claim at no charge. The Alendronic Acid recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Alendronate Sodium

dom — Fri, 23 Sep 2011 14:19:53 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ALENDRONATE SODIUM, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Alendronate sodium, also known as alendronic acid, is a drug manufactured by Merck to be used in the treatment of osteoporosis, along with several other types of bone disease. It is a bisphosphonate that Merck held the patent on until 2008, when the company lost the many appeals filed in an effort to block others from creating an FDA approved generic version of alendronate sodium.

Alendronate sodium is mainly used in the treatment of osteoporosis in females; however, it can also be used to treat osteoporosis in males. It has also been used in conjunction with vitamin D and calcium for the treatment and prevention of osteoporosis that is corticosteroid-related. In addition, it has also proven to be somewhat effective in the treatment of Paget’s disease.

Clinical data has shown that the bone turnover rate has been normalized with the use of alendronate sodium in post-menopausal women, resulting in increased bone density in the hip, spine, wrist and overall body. Data shows that alendronate sodium has actually decreased the fracture risk in women who were in the highest risk bracket by 50% on average.

Alendronate sodium has been contraindicated in several instances, such as in clinical manifestations of osteomalacia, hypocalcemia, those with an alendronate hypersensitivity issue, women that are breastfeeding or pregnant and patients that are unable to walk, sit or stand after 30 minutes following oral administration. In addition, patients with esophagitis, gastric ulserations or gastritis, renal impairment, strictures or achalasia and any patients under age 18 are cautioned against the use of this medication.

Side Effects of alendronate sodium

Alendronate sodium has several side effects associated with its use. The most common of these side effects are:

Back pain
Bloating
Changes in taste
Constipation
Diarrhea
Dizziness
Full feeling
Flu-like symptoms
Gas
Headache
Joint pain
Muscle pain
Nausea
Vomiting

The more serious side effects of alendronate sodium is what physicians and patients alike should be most concerned with. The more severe of alendronate sodium’s side effects include:

If patients consume milk, supplements or other drugs that contain large amounts of calcium, aluminum or magnesium, alendronate sodium resorption is decreased. HRT has not been proven to cause any drug-drug interactions, nor have any been noted with fluorides or D analogues, although concomitant treatment should be avoided. In addition, NSAIDs combined with alendronate sodium may actually elevate the risk for gastric ulcers.

If you have experienced serious side effects as a result of taking alendronate sodium, a lawyer with experience in the ongoing alendronate sodium litigation can help evaluate your claim at no charge. The alendronate sodium recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Fosamax®

dom — Fri, 23 Sep 2011 14:10:47 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY FOSAMAX, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Fosamax, also known as alendronate sodium and alendronic acid, is a drug manufactured by Merck to be used in the treatment of osteoporosis, along with several other types of bone disease. It is a bisphosphonate that Merck held the patent on until 2008, when the company lost the many appeals filed in an effort to block others from creating an FDA approved generic version of Fosamax.

Fosamax is mainly used in the treatment of osteoporosis in females; however, it can also be used to treat osteoporosis in males. It has also been used in conjunction with vitamin D and calcium for the treatment and prevention of osteoporosis that is corticosteroid-related. In addition, it has also proven to be somewhat effective in the treatment of Paget’s disease.

Clinical data has shown that the bone turnover rate has been normalized with the use of Fosamax in post-menopausal women, resulting in increased bone density in the hip, spine, wrist and overall body. Data shows that Fosamax has actually decreased the fracture risk in women who were in the highest risk bracket by 50% on average.

Fosamax has been contraindicated in several instances, such as in clinical manifestations of osteomalacia, hypocalcemia, those with an alendronate hypersensitivity issue, women that are breastfeeding or pregnant and patients that are unable to walk, sit or stand after 30 minutes following oral administration. In addition, patients with esophagitis, gastric ulserations or gastritis, renal impairment, strictures or achalasia and any patients under age 18 are cautioned against the use of this medication.

Side Effects of Fosamax

Fosamax has several side effects associated with its use. The most common of these side effects are:

Back pain
Bloating
Changes in taste
Constipation
Diarrhea
Dizziness
Full feeling
Flu-like symptoms
Gas
Headache
Joint pain
Muscle pain
Nausea
Vomiting

The more serious side effects of Fosamax is what physicians and patients alike should be most concerned with. The more severe of Fosamax’s side effects include:

If patients consume milk, supplements or other drugs that contain large amounts of calcium, aluminum or magnesium, Fosamax resorption is decreased. HRT has not been proven to cause any drug-drug interactions, nor have any been noted with fluorides or D analogues, although concomitant treatment should be avoided. In addition, NSAIDs combined with Fosamax may actually elevate the risk for gastric ulcers.

If you have experienced serious side effects as a result of taking Fosamax, a lawyer with experience in the ongoing Fosamax litigation can help evaluate your claim at no charge. The Fosamax recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Ortho Evra®

dom — Fri, 23 Sep 2011 05:19:29 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ORTHO EVRA, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Birth control pills are how women prevent from becoming pregnant. There are several forms of contraceptives and Ortho Evra is another form. This product comes as a patch and is worn and changed every week. The patch contains estrogen as well as progestin that help prevent pregnancy. It is applied to the skin one time each week and women do this for 3 weeks straight, then, come the fourth week, there is no patch to be worn. This is the week when your menstruation occurs.

Hormones are released inside of a woman’s bloodstream to help with preventing pregnancy just as with birth control pills and the shot. The Ortho Evra patch helps with suppressing the body’s ovulation, which occurs when the body releases an egg into the uterus for possible fertilization. A woman’s uterine lining will also be thickened to prevent her partner’s sperm from getting to her egg. There is no protection against STDs.

Risks Associated with Ortho Evra

There are some side effects that come with all birth control, and for Ortho Evra they include:

· Irritation to the skin
· Tenderness in the breast
· Muscle spasms
· Acne
· Diarrhea
· Feeling fatigued all the time
· Mood swings
· Unexplained weight gain
· Nausea
· Spotting or bleeding
· Migraines

There have been recent scientific studies that have shown that this contraceptive produces a higher level of hormones that will circulate around in a woman’s body opposed to other contraceptive alternatives. Because of that issue, there may be an increased risk of experiencing some of the named side effects while using the patch.

The Ortho Evra contraceptive received approval and certification from the FDA in the year 2001. However, in the year 2005, there were a reported dozen deaths from taking this contraceptive. In the year 2004, there were over 4 million people in the US alone that had tried the patch.

About a dozen females died with age ranges in the late teens and early twenties. The Associated Press additionally reported that there were about 12 cases that were blood clot related and ended up in deaths, out of the 800,000 people who had used this birth control in the year 2004.

Lawsuits

Ortho Evra has become responsible for thrombosis as well as strokes in some individuals and for that reasons lawsuits have been filed against this patch. On September 2, 2005 there was a lawsuit filed by a woman from Georgia who was using the patch and suffered a pulmonary embolism that she believed was the result of taking Ortho Evra. She believed that the company who manufactures this product promoted the product knowing it caused health risks in women, as well as failing to inform users that there was an increased risk with issues such as blood clots,
among others.

There was yet another case that resulted in a mother having a stroke, which resulted in being paralyzed, and this case aired on national TV.

If you have experienced serious side effects as a result of taking Ortho Evra, a lawyer with experience in the ongoing Ortho Evra litigation can help evaluate your claim at no charge. The Ortho Evra recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Varenicline

dom — Fri, 23 Sep 2011 04:46:06 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY VARENICLINE, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Varenicline, also known as Chantix or Champix, is a drug used in the treatment of smoking addiction. The drug is manufactured by Pfizer as an oral tablet that is available by prescription only. The drug acts to stimulate the nicotine receptors in a weaker manner than nicotine, making it a partial agonist. However, as it is a partial agonist, its actions decrease the feelings of pleasure that smokers get when smoking cigarettes and it also reduces the cravings. The combination of these mechanisms has assisted many to effectively stop smoking.

The FDA slated varenicline, the main component in Champix and Chantix, for priority review in February of 2006. After just 6 months of review due to the drug’s clearly demonstrated effectiveness during clinical trials, as well as its lack at the time of any safety issues, the drug was made available to the United States market on the 1st of August in 2006. Just under two months later, the European Union approved the drug for sale.

Varenicline has been FDA approved for up to 12 weeks of use. If the patient has successfully stopped smoking, the drug can be continued under the physician’s direction for up to 12 additional weeks. However, the drug cannot be prescribed to patients who are pregnant or under 18 years of age. In addition, Varenicline may be present in breast milk of breastfeeding mothers; thus, it is not recommended for use in patients of this nature due to the unknown effects is could have on infants.

Side Effects of Varenicline

Varenicline, like several other pharmaceuticals, has several common side effects that are associated with its use. These include the following:

· Abdominal pain
· Abnormal dreams
· Constipation
· Difficulty sleeping
· Flatulence
· Headache
· Taste changes
· Vomiting

More serious side effects of Varenicline have also been noted. As a result, the FDA made an announcement regarding these symptoms and required that Pfizer update the information to inform physicians and patients to these more severe symptoms. These side effects include:

· Agitation
· Behavior changes
· Depressed mood
· Drowsiness
· Erratic behavior
· Suicidal behavior
· Suicidal ideation
· Other neuropsychiatric symptoms
· Cardiovascular events

FDA WARNING

In July of 2009, the FDA issued the strongest warning possible for Varenicline, forcing the manufacturer to place a black box warning on the drug’s packaging and inserts to alert the public to these severe side effects. In June of 2011, the drug was under the spotlight again when the FDA announced that it might be associated with adverse cardiovascular events in users that are already suffering from cardiovascular disease.

Varenicline has met with controversy since its release on the market. In September of 2007, a musician named Carter Albrecht was killed after acting erratically while on verenicline. Later that year, the FDA received additional reports of similar experiences by others taking drugs containing verenicline. Then, in May of 2008, the FAA announced a ban on the drug for air traffic controllers and pilots, citing concerns with neuropsychiatric effects that could put public safety at risk. These are just a few of the reported controversial issues, as many more exist.

If you have experienced serious side effects as a result of taking Varenicline, a lawyer with experience in the ongoing Varenicline litigation can help evaluate your claim at no charge. The Varenicline recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Champix®

dom — Fri, 23 Sep 2011 04:17:51 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY CHAMPIX, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Champix, also known as varenicline and Chantix, is a drug used in the treatment of smoking addiction. The drug is manufactured by Pfizer as an oral tablet that is available by prescription only. The drug acts to stimulate the nicotine receptors in a weaker manner than nicotine, making it a partial agonist. However, as it is a partial agonist, its actions decrease the feelings of pleasure that smokers get when smoking cigarettes and it also reduces the cravings. The combination of these mechanisms has assisted many to effectively stop smoking.

The FDA slated varenicline, the main component in Champix, for priority review in February of 2006. After just 6 months of review due to the drug’s clearly demonstrated effectiveness during clinical trials, as well as its lack at the time of any safety issues, the drug was made available to the United States market on the 1st of August in 2006. Just under two months later, the European Union approved the drug for sale.

Chantix has been FDA approved for up to 12 weeks of use. If the patient has successfully stopped smoking, the drug can be continued under the physician’s direction for up to 12 additional weeks. However, the drug cannot be prescribed to patients who are pregnant or under 18 years of age. In addition, Champix may be present in breast milk of breastfeeding mothers; thus, it is not recommended for use in patients of this nature due to the unknown effects is could have on infants.

Side Effects of Champix

Champix, like several other pharmaceuticals, has several common side effects that are associated with its use. These include the following:

· Abdominal pain
· Abnormal dreams
· Constipation
· Difficulty sleeping
· Flatulence
· Headache
· Taste changes
· Vomiting

More serious side effects of Champix have also been noted. As a result, the FDA made an announcement regarding these symptoms and required that Pfizer update the information to inform physicians and patients to these more severe symptoms. These side effects include:

· Agitation
· Behavior changes
· Depressed mood
· Drowsiness
· Erratic behavior
· Suicidal behavior
· Suicidal ideation
· Other neuropsychiatric symptoms
· Cardiovascular events

FDA WARNING

In July of 2009, the FDA issued the strongest warning possible for Champix, forcing the manufacturer to place a black box warning on the drug’s packaging and inserts to alert the public to these severe side effects. In June of 2011, the drug was under the spotlight again when the FDA announced that it might be associated with adverse cardiovascular events in users that are already suffering from cardiovascular disease.

Champix has met with controversy since its release on the market. In September of 2007, a musician named Carter Albrecht was killed after acting erratically while on verenicline. Later that year, the FDA received additional reports of similar experiences by others taking drugs containing verenicline. Then, in May of 2008, the FAA announced a ban on the drug for air traffic controllers and pilots, citing concerns with neuropsychiatric effects that could put public safety at risk. These are just a few of the reported controversial issues, as many more exist.

If you have experienced serious side effects as a result of taking Champix, a lawyer with experience in the ongoing Champix litigation can help evaluate your claim at no charge. The Champix recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Chantix®

dom — Fri, 23 Sep 2011 04:12:10 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY CHANTIX, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Chantix, also known as varenicline and Champix, is a drug used in the treatment of smoking addiction. The drug is manufactured by Pfizer as an oral tablet that is available by prescription only. The drug acts to stimulate the nicotine receptors in a weaker manner than nicotine, making it a partial agonist. However, as it is a partial agonist, its actions decrease the feelings of pleasure that smokers get when smoking cigarettes and it also reduces the cravings. The combination of these mechanisms has assisted many to effectively stop smoking.

The FDA slated varenicline, the main component in Chantix, for priority review in February of 2006. After just 6 months of review due to the drug’s clearly demonstrated effectiveness during clinical trials, as well as its lack at the time of any safety issues, the drug was made available to the United States market on the 1st of August in 2006. Just under two months later, the European Union approved the drug for sale.

Chantix has been FDA approved for up to 12 weeks of use. If the patient has successfully stopped smoking, the drug can be continued under the physician’s direction for up to 12 additional weeks. However, the drug cannot be prescribed to patients who are pregnant or under 18 years of age. In addition, Chantix may be present in breast milk of breastfeeding mothers; thus, it is not recommended for use in patients of this nature due to the unknown effects is could have on infants.

Side Effects of Chantix

Chantix, like several other pharmaceuticals, has several common side effects that are associated with its use. These include the following:

· Abdominal pain
· Abnormal dreams
· Constipation
· Difficulty sleeping
· Flatulence
· Headache
· Taste changes
· Vomiting

More serious side effects of Chantix have also been noted. As a result, the FDA made an announcement regarding these symptoms and required that Pfizer update the information to inform physicians and patients to these more severe symptoms. These side effects include:

· Agitation
· Behavior changes
· Depressed mood
· Drowsiness
· Erratic behavior
· Suicidal behavior
· Suicidal ideation
· Other neuropsychiatric symptoms
· Cardiovascular events

FDA WARNING

In July of 2009, the FDA issued the strongest warning possible for Chantix, forcing the manufacturer to place a black box warning on the drug’s packaging and inserts to alert the public to these severe side effects. In June of 2011, the drug was under the spotlight again when the FDA announced that it might be associated with adverse cardiovascular events in users that are already suffering from cardiovascular disease.

Chantix has met with controversy since its release on the market. In September of 2007, a musician named Carter Albrecht was killed after acting erratically while on verenicline. Later that year, the FDA received additional reports of similar experiences by others taking drugs containing verenicline. Then, in May of 2008, the FAA announced a ban on the drug for air traffic controllers and pilots, citing concerns with neuropsychiatric effects that could put public safety at risk. These are just a few of the reported controversial issues, as many more exist.

If you have experienced serious side effects as a result of taking Chantix, a lawyer with experience in the ongoing Chantix litigation can help evaluate your claim at no charge. The Chantix recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Exenatide

dom — Fri, 23 Sep 2011 03:44:21 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY EXENATIDE, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Exenatide is a drug used to treat diabetes mellitus (type 2 diabetes). The drug is manufactured by Eli Lilly and Amylin Pharmaceuticals and was approved by the FDA in 2005. The drug itself is synthetic exendin-4. Though the drug is synthetic, it is created to mirror the hormone that was located in the Gila monster’s saliva. Exenatide acts similarly to glucagon-like peptide-1 in humans and regulates insulin secretion and glucose metabolism.

The drug is available as a subcutaneous injection that is typically given twice daily, an hour prior to the patient’s first and last meals. The injection can be given in the arm, thigh or the abdomen and is believed to assist in glucose control five different ways. The first is by augmenting the pancreas response. The second is by suppressing glucagon release in the pancreas. The third is by slowing gastric emptying. The fourth is by reducing appetite and promoting satiety through hypothalamic receptors. Finally, the fifth is by reducing the fat content of the liver.

One of the biggest advantages of Exenatide is that it controls glucose while not promoting weight gain. However, the disadvantages can be adverse gastrointestinal reactions, among other side effects. To get an idea of some of the side effects that this drug involves, you can review the adverse reactions section below.

Adverse Reactions of Exenatide

Exenatide has several negative side effects associated with its use. These range from common side effects that are not that serious to the more severe, but rare side effects. This list is not complete; however, it should give you a general idea of what to expect when taking Exenatide. These side effects include:

Nausea
Indigestion
Sour stomach
Diarrhea
Vomiting
Heartburn
Belching
Headache
Dizziness
Jittery feeling
Possible increase for thyroid cancer
Pancreatitis
Hypoglycemia

FDA WARNING

In 2007, a warning was added to Exenatide labeling at the FDA’s request. The warning informed patients that the drug may cause acute pancreatitis. In 2010, the FDA again became concerned over the side effects of Exenatide due to reports that the drug’s use may increase the patient’s risk for thyroid cancer. However, the final decision was delayed when the FDA decided to ask the manufacturers, Eli Lilly and Amylin, for additional information. It is highly likely that these new findings will cause the drug to be issued what is known as a black box warning, which is the strictest FDA required caution for pharmaceuticals.

Lawsuits have already been filed against the makers of Exenatide. The first lawsuit on record was filed in 2008 by a man from Virginia. Although the details of the suit are not yet fully known, the man’s attorney stated that the 2007 change of label was inadequate. However, several additional lawsuits are expected, as some of the more severe side effects of this drug have resulted in death and long term care. If you or a loved one has experienced any severe side effects of Exenatide, seek medical assistance immediately.

If you have experienced serious side effects as a result of taking Exenatide, a lawyer with experience in the ongoing Exenatide litigation can help evaluate your claim at no charge. The Exenatide recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Byetta®

dom — Fri, 23 Sep 2011 03:36:16 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY BYETTA, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Byetta, also known as Exenatide, is a drug used to treat diabetes mellitus (type 2 diabetes). The drug is manufactured by Eli Lilly and Amylin Pharmaceuticals and was approved by the FDA in 2005. The drug itself is synthetic exendin-4. Though the drug is synthetic, it is created to mirror the hormone that was located in the Gila monster’s saliva. Byetta acts similarly to glucagon-like peptide-1 in humans and regulates insulin secretion and glucose metabolism.

One of the biggest advantages of Byetta is that it controls glucose while not promoting weight gain. However, the disadvantages can be adverse gastrointestinal reactions, among other side effects. To get an idea of some of the side effects that this drug involves, you can review the adverse reactions section below.

Adverse Reactions of Byetta

Byetta has several negative side effects associated with its use. These range from common side effects that are not that serious to the more severe, but rare side effects. This list is not complete; however, it should give you a general idea of what to expect when taking Byetta. These side effects include:

Nausea
Indigestion
Sour stomach
Diarrhea
Vomiting
Heartburn
Belching
Headache
Dizziness
Jittery feeling
Possible increase for thyroid cancer
Pancreatitis
Hypoglycemia

FDA WARNING

In 2007, a warning was added to Byetta labeling at the FDA’s request. The warning informed patients that the drug may cause acute pancreatitis. In 2010, the FDA again became concerned over the side effects of Byetta due to reports that the drug’s use may increase the patient’s risk for thyroid cancer. However, the final decision was delayed when the FDA decided to ask the manufacturers, Eli Lilly and Amylin, for additional information. It is highly likely that these new findings will cause the drug to be issued what is known as a black box warning, which is the strictest FDA required caution for pharmaceuticals.

Lawsuits have already been filed against the makers of Byetta. The first lawsuit on record was filed in 2008 by a man from Virginia. Although the details of the suit are not yet fully known, the man’s attorney stated that the 2007 change of label was inadequate. However, several additional lawsuits are expected, as some of the more severe side effects of this drug have resulted in death and long term care. If you or a loved one has experienced any severe side effects of Byetta, seek medical assistance immediately.

If you have experienced serious side effects as a result of taking Byetta, a lawyer with experience in the ongoing Byetta litigation can help evaluate your claim at no charge. The Byetta recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Denture Creams

dom — Fri, 23 Sep 2011 03:17:19 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ANY OF THE LEADING DENTURE CREAMS, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

What is all the fuss about those late night denture cream “poisoning” commercials you may be seeing on TV? To make a long story short, denture creams may be causing severe nerve damage because of zinc poisoning. Consumer aware.

POLYGRIP

Polygrip has been a popular denture adhesive for decades. Countless millions have relied on this product, manufactured by pharmaceutical giant GlaxoSmithKline, to hold their dentures in place. The adhesive is an over the counter product and it is typically beaded into the portion of an individual’s dentures that make contact with the gums. This allows the dentures to better adhere to the gums, which allows denture wearers to eat better, speak better and simply have more confidence and less embarrassment associated with their dentures.

However, several very serious side effects have been found to be associated with the use of Poligrip, as well as many other popular denture creams. In fact, several lawsuits have already been filed and some have already been settled for confidential amounts outside of a courthouse.

In February of 2010, GlaxoSmithKline announced the discontinuation of the denture adhesive, Super Poligrip. The versions that will be discontinued are those containing zinc. So it should come as no surprise that the discontinuation was due to several lawsuits being filed against GlaxoSmithKline for zinc poisoning. GlaxoSmithKline did announce that Super Poligrip Original, Ultra Fresh andExtra Care would be replaced with alternatives that were free of zinc.

Unfortunately, the company had for years claimed that the zinc present in Poligrip didn’t pose a risk to consumers. They have now finally acknowledged that these popular denture adhesives do pose a risk for neuropathy, zinc poisoning and other various neurological issues.

The zinc present in Poligrip is able to deplete the levels of copper in the body as a result of high levels of zinc being able to enter the consumer’s body. This increase of zinc and depletion of copper results in symptoms, which include:

· Difficulty walking
· Dizziness
· Loss of balance
· Loss of sensation
· Muscle weakness
· Numbness
· Pain
· Paralysis
· Tingling
· Unexplained pain

Unfortunately, many of the people that have been experiencing these symptoms are elderly individuals that have been using Poligripfor years but have simply associated the symptoms with old age instead of an issue with their health. Those that have experienced some of the more serious side effects of using Poligrip have realized that something wasn’t right with their health and sought medical attention. However, in most cases, the physicians of these individuals have run them through an entire barrage of tests in an attempt to find the source of the issue.

Many that have experienced the more severe side effects, such as paralysis, muscle weakness and loss of balance have had to quit working and, in several instances, now require care or assistance to complete their daily activities of living. This makes it all the more important to be aware of the symptoms if you are a Poligrip user. Should you be experiencing or begin to experience any of the symptoms mentioned, you should seek medical attention immediately. In addition, if you feel that you should be entitled to compensation due to using Poligrip, get in touch with an attorney.

If you have experienced serious side effects as a result of taking Polygrip, a lawyer with experience in the ongoing Polygrip litigation can help evaluate your claim at no charge. The Polygrip recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

FIXODENT

If you have been a victim of Fixodent and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Fixodent is one of the popular choices of denture adhesives and it has been available for decades. In fact, there are likely millions of individuals that have purchased and used this adhesive to assist them in affixing their dentures on a daily basis. What many consumers do not realize is that Fixodent is currently one of the two popular brands of denture adhesives that have been causing some extremely serious health issues in those who use it.

There are somewhere in the vicinity of 35 million people in the United States that use a denture adhesive to help their dentures stay in place. However, the amount of product used varies by the person using it. It is possible that excessive and prolonged use may play a larger role in the side effects experienced by patients using Fixodent. In fact, studies have determined that people using larger amounts of Fixodent over several years have a higher likelihood of actually experiencing the side effects than those who use smaller amounts of the adhesive.

In August of 2008, a study conducted reported that there were four patients, all of whom wore dentures, which were afflicted with neuropathy. Other various neurological issues were also reported in these patients. Each of the patients reported had blood tests conducted and each test came back with unusually high zinc levels and unusually low copper levels. Researchers ruled out the array of potential causes, concluding that the result of the levels might have been the zinc present in their denture cream.

Although GlaxoSmithKline, the makers of Polygrip, have pulled their product from the market and announced that all of their zinc-containing products would be replaced with alternatives free of zinc, the makers of Fixodent have yet to follow suit. In fact, not only has Proctor & Gamble refused to pull their product from the shelves by issuing a recall, but they have yet to provide even a warning to the public regarding the risk of excessive zinc exposure. The even more surprising thing is that Fixodent hasn’t even listed zinc as an ingredient in their product!

These deceptive practices and negligence in making the consumer aware may result in countless scores of costly lawsuits for Proctor & Gamble in the future, as no recall means that millions may be continuing to use the product. Countless consumers have reported neuropathy and other neurological issues. The symptoms of these issues generally include the following:

· Inability to walk or decrease in stride
· Increase in stumbling or falling
· Loss of sensation
· Loss of strength, typically in the feet and/or legs
· Numbness
· Tingling
· Unexplained pain

Any person experiencing any of the symptoms mentioned above should contact their physician immediately. If you believe that your issue is caused by the denture cream you have been using, a simple blood test can determine whether or not you have a copper deficiency and an increased level of zinc present. If this is the case and you are interested in receiving compensation for what you’ve been through, several skilled attorneys are currently handling Fixodent cases.

If you have experienced serious side effects as a result of taking denture creams, a lawyer with experience in the ongoing denture cream litigation can help evaluate your claim at no charge. The denture cream recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Fixodent®

dom — Fri, 23 Sep 2011 03:08:07 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY FIXODENT, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

· Inability to walk or decrease in stride
· Increase in stumbling or falling
· Loss of sensation
· Loss of strength, typically in the feet and/or legs
· Numbness
· Tingling
· Unexplained pain

If you have experienced serious side effects as a result of taking Fixodent, a lawyer with experience in the ongoing Fixodent litigation can help evaluate your claim at no charge. The Fixodent recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Polygrip®

dom — Thu, 22 Sep 2011 21:22:13 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY POLYGRIP, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

In February of 2010, GlaxoSmithKline announced the discontinuation of the denture adhesive, Super Poligrip. The versions that will be discontinued are those containing zinc. So it should come as no surprise that the discontinuation was due to several lawsuits being filed against GlaxoSmithKline for zinc poisoning. GlaxoSmithKline did announce that Super Poligrip Original, Ultra Fresh and Extra Care would be replaced with alternatives that were free of zinc.

· Difficulty walking
· Dizziness
· Loss of balance
· Loss of sensation
· Muscle weakness
· Numbness
· Pain
· Paralysis
· Tingling
· Unexplained pain

Unfortunately, many of the people that have been experiencing these symptoms are elderly individuals that have been using Poligrip for years but have simply associated the symptoms with old age instead of an issue with their health. Those that have experienced some of the more serious side effects of using Poligrip have realized that something wasn’t right with their health and sought medical attention. However, in most cases, the physicians of these individuals have run them through an entire barrage of tests in an attempt to find the source of the issue.

Sotret®

dom — Thu, 22 Sep 2011 20:43:47 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY SOTRET, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Sotret is a drug that is used for treating severe cases of acne. The drug has also been used to treat other skin conditions and cancers over the years. Initially, this drug was developed for chemo therapies to help with treating brain cancer as well as pancreatic cancer. It is still being used for these conditions as it has been shown to help kill off the cells that divide rapidly. It can additionally be used for treating ichthyosis, which happens is a form of a skin deformation.

Side Effects of Sotret

There is scientific data that has shown there are higher risks of birth defects if Sotret is taken during pregnancy. Women who are at their reproductive age may be recommended to stay away from this medication and any other forms of isotretinoin medications.

The drug Accutane was removed from the market. Another significant side effect stems from risks of severe mental problems including depression, psychosis and even suicide. Hallucinations are also common while taking Accutane.

If you have experienced serious side effects as a result of taking Sotret/Rosiglitazone, a lawyer with experience in the ongoing Rosiglitazone litigation can help evaluate your claim at no charge. The Sotret recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Roaccutane®

dom — Thu, 22 Sep 2011 20:37:50 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ROACCUTANE, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Roaccutane is a drug that is used for treating severe cases of acne. The drug has also been used to treat other skin conditions and cancers over the years. Initially, this drug was developed for chemo therapies to help with treating brain cancer as well as pancreatic cancer. It is still being used for these conditions as it has been shown to help kill off the cells that divide rapidly. It can additionally be used for treating ichthyosis, which happens is a form of a skin deformation.

Side Effects of Roaccutane

There is scientific data that has shown there are higher risks of birth defects if Roaccutane is taken during pregnancy. Women who are at their reproductive age may be recommended to stay away from this medication and any other forms of isotretinoin medications.

If you have experienced serious side effects as a result of taking Roaccutane/Rosiglitazone, a lawyer with experience in the ongoing Rosiglitazone litigation can help evaluate your claim at no charge. The Roaccutane recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Oratane®

dom — Thu, 22 Sep 2011 08:35:27 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ORATANE, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Oratane is a drug that is used for treating severe cases of acne. The drug has also been used to treat other skin conditions and cancers over the years. Initially, this drug was developed for chemo therapies to help with treating brain cancer as well as pancreatic cancer. It is still being used for these conditions as it has been shown to help kill off the cells that divide rapidly. It can additionally be used for treating ichthyosis, which happens is a form of a skin deformation.

Side Effects of Oratane

There is scientific data that has shown there are higher risks of birth defects if Oratane is taken during pregnancy. Women who are at their reproductive age may be recommended to stay away from this medication and any other forms of isotretinoin medications.

If you have experienced serious side effects as a result of taking Oratane/Rosiglitazone, a lawyer with experience in the ongoing Rosiglitazone litigation can help evaluate your claim at no charge. The Oratane recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Isotrex®

dom — Thu, 22 Sep 2011 08:29:45 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ISOTREX, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Isotrex is a drug that is used for treating severe cases of acne. The drug has also been used to treat other skin conditions and cancers over the years. Initially, this drug was developed for chemo therapies to help with treating brain cancer as well as pancreatic cancer. It is still being used for these conditions as it has been shown to help kill off the cells that divide rapidly. It can additionally be used for treating ichthyosis, which happens is a form of a skin deformation.

Side Effects of Isotrex

There is scientific data that has shown there are higher risks of birth defects if Isotrex is taken during pregnancy. Women who are at their reproductive age may be recommended to stay away from this medication and any other forms of isotretinoin medications.

If you have experienced serious side effects as a result of taking Isotrex/Rosiglitazone, a lawyer with experience in the ongoing Rosiglitazone litigation can help evaluate your claim at no charge. The Isotrex recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Isotrexin®

dom — Thu, 22 Sep 2011 08:23:17 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ISOTREXIN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Isotrexin is a drug that is used for treating severe cases of acne. The drug has also been used to treat other skin conditions and cancers over the years. Initially, this drug was developed for chemo therapies to help with treating brain cancer as well as pancreatic cancer. It is still being used for these conditions as it has been shown to help kill off the cells that divide rapidly. It can additionally be used for treating ichthyosis, which happens is a form of a skin deformation.

Side Effects of Isotrexin

There is scientific data that has shown there are higher risks of birth defects if Isotrexin is taken during pregnancy. Women who are at their reproductive age may be recommended to stay away from this medication and any other forms of isotretinoin medications.

If you have experienced serious side effects as a result of taking Isotrexin/Rosiglitazone, a lawyer with experience in the ongoing Rosiglitazone litigation can help evaluate your claim at no charge. The Isotrexin recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Isotretinoin

dom — Thu, 22 Sep 2011 08:15:42 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ISOTRETINOIN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Isotretinoin is a drug that is used for treating severe cases of acne. The drug has also been used to treat other skin conditions and cancers over the years. Initially, this drug was developed for chemo therapies to help with treating brain cancer as well as pancreatic cancer. It is still being used for these conditions as it has been shown to help kill off the cells that divide rapidly. It can additionally be used for treating ichthyosis, which happens is a form of a skin deformation.

Side Effects of Isotretinoin

There is scientific data that has shown there are higher risks of birth defects if Isotretinoin is taken during pregnancy. Women who are at their reproductive age may be recommended to stay away from this medication and any other forms of isotretinoin medications.

If you have experienced serious side effects as a result of taking Isotretinoin/Rosiglitazone, a lawyer with experience in the ongoing Rosiglitazone litigation can help evaluate your claim at no charge. The Isotretinoin recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

ISOTRET®

dom — Thu, 22 Sep 2011 08:07:00 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ISOTRET, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

ISOTRET is a drug that is used for treating severe cases of acne. The drug has also been used to treat other skin conditions and cancers over the years. Initially, this drug was developed for chemo therapies to help with treating brain cancer as well as pancreatic cancer. It is still being used for these conditions as it has been shown to help kill off the cells that divide rapidly. It can additionally be used for treating ichthyosis, which happens is a form of a skin deformation.

Side Effects of ISOTRET

There is scientific data that has shown there are higher risks of birth defects if ISOTRET is taken during pregnancy. Women who are at their reproductive age may be recommended to stay away from this medication and any other forms of isotretinoin medications.

If you have experienced serious side effects as a result of taking ISOTRET/Rosiglitazone, a lawyer with experience in the ongoing Rosiglitazone litigation can help evaluate your claim at no charge. The ISOTRET recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Isotane®

dom — Thu, 22 Sep 2011 07:54:47 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ISOTANE, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Isotane is a drug that is used for treating severe cases of acne. The drug is also known as isotretinoin and has also been used to treat other skin conditions and cancers over the years. Initially, this drug was developed for chemo therapies to help with treating brain cancer as well as pancreatic cancer. It is still being used for these conditions as it has been shown to help kill off the cells that divide rapidly. It can additionally be used for treating ichthyosis, which happens is a form of a skin deformation.

Side Effects of Isotane

There is scientific data that has shown there are higher risks of birth defects if Isotane is taken during pregnancy. Women who are at their reproductive age may be recommended to stay away from this medication and any other forms of isotretinoin medications.

If you have experienced serious side effects as a result of taking Isotane/Rosiglitazone, a lawyer with experience in the ongoing Rosiglitazone litigation can help evaluate your claim at no charge. The Isotane recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Decutan®

dom — Thu, 22 Sep 2011 07:50:55 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY DECUTAN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Decutan is a drug that is used for treating severe cases of acne. The drug is also known as isotretinoin and has also been used to treat other skin conditions and cancers over the years. Initially, this drug was developed for chemo therapies to help with treating brain cancer as well as pancreatic cancer. It is still being used for these conditions as it has been shown to help kill off the cells that divide rapidly. It can additionally be used for treating ichthyosis, which happens is a form of a skin deformation.

Side Effects of Decutan

There is scientific data that has shown there are higher risks of birth defects if Decutan is taken during pregnancy. Women who are at their reproductive age may be recommended to stay away from this medication and any other forms of isotretinoin medications.

If you have experienced serious side effects as a result of taking Decutan/Rosiglitazone, a lawyer with experience in the ongoing Rosiglitazone litigation can help evaluate your claim at no charge. The Decutan recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Amnesteem®

dom — Thu, 22 Sep 2011 07:40:32 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY AMNESTEEM, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Amnesteem is a drug that is used for treating severe cases of acne. The drug is also known as isotretinoin and has also been used to treat other skin conditions and cancers over the years. Initially, this drug was developed for chemo therapies to help with treating brain cancer as well as pancreatic cancer. It is still being used for these conditions as it has been shown to help kill off the cells that divide rapidly. It can additionally be used for treating ichthyosis, which happens is a form of a skin deformation.

Side Effects of Amnesteem

There is scientific data that has shown there are higher risks of birth defects if Amnesteem is taken during pregnancy. Women who are at their reproductive age may be recommended to stay away from this medication and any other forms of isotretinoin medications.

Amnesteem was removed from the market. Another significant side effect stems from risks of severe mental problems including depression, psychosis and even suicide. Hallucinations are also common while taking Accutane.

If you have experienced serious side effects as a result of taking Amnesteem/Rosiglitazone, a lawyer with experience in the ongoing Rosiglitazone litigation can help evaluate your claim at no charge. The Amnesteem recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Accutane®

dom — Thu, 22 Sep 2011 07:28:56 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ACCUTANE, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Accutane is a drug that is used for treating severe cases of acne. The drug is also known as isotretinoin and has also been used to treat other skin conditions and cancers over the years. Initially, this drug was developed for chemo therapies to help with treating brain cancer as well as pancreatic cancer. It is still being used for these conditions as it has been shown to help kill off the cells that divide rapidly. It can additionally be used for treating ichthyosis, which happens is a form of a skin deformation.

Side Effects of Accutane

There is scientific data that has shown there are higher risks of birth defects if Accutane is taken during pregnancy. Women who are at their reproductive age may be recommended to stay away from this medication and any other forms of isotretinoin medications.

Accutane was removed from the market. Another significant side effect stems from risks of severe mental problems including depression, psychosis and even suicide. Hallucinations are also common while taking Accutane.

If you have experienced serious side effects as a result of taking Accutane/Rosiglitazone, a lawyer with experience in the ongoing Rosiglitazone litigation can help evaluate your claim at no charge. The Accutane recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Rosiglitazone

dom — Thu, 22 Sep 2011 04:56:17 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ROSIGLITAZONE, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Rosiglitazone and is a form of drug that has been designed to help with treating diabetes. It helps with lowering and balancing your sugar levels especially in those who have type 2 diabetes. This drug should be taken along with having an exercise routine in play to help control levels of your blood’s sugar.

Uses of Rosiglitazone

This medication is classified as a diabetic medication, which signifies that diabetic symptoms are going to be treated. Many sufferers experience blood sugar levels that always move up and down and this is especially true after a meal or a snack. This medication was designed to prevent patients from feeling faint, weak, emotional or just full of too much energy.

Medical professionals advise that patients should not begin taking this unless all other alternatives and options have been exhausted. This is an option that is only used on those who are not dependant on insulin. For anyone with type 1 diabetes, this is a drug you should refrain from taking. This medication works to help balance out the body’s level of insulin and its natural response.

Side Effects of Rosiglitazone

There are several side effects that patients may experience while taking this medication and can include:

· Cough
· Headache
· Dizziness
· Swelling
· Rash
· Difficulty breathing
· Rapid heartbeat
· Itching
· Fluid retention
· CHF
· High cholesterol
· High blood pressure
· Dry cough
· Increased tired feeling

There may be other side effects that patients experience and can vary from one person to another. If you experience dark urine or tingling in your feet or your hands you should stop taking this medication right away.

Lawsuits

There are lawsuits against Avandia (Rosiglitazone) as there are some patients that claim they became injured after using this drug. There are many individual claims that are being filed and a patient wins the case if they can prove that there were injuries that were caused as a result of taking this medication. Also, the patient or doctor needs to inform Glaxo Smith of these effects and of their severity.

If you develop CHF, stroke, liver toxicity, heart attack, or an allergic reaction, this will likely get you compensation in return. For those who have a partner or loved one that was on this medication and resulted in death, there are monetary settlements available to you. If there was a death, the best option is to file an individual case as opposed to filing a joint one.

Avandia (Rosiglitazone) has recently become more of a hot topic as the FDA has issued warnings based on the side effect of this medication. While there are benefits to those with type 2 diabetes, the side effects can be life threatening. There can be bone fractures as well as stroke which can do damage to an individual. Due to the side effects and the fact that they can be life threatening, the FDA over time may set a complete recall of this medication which will remove it entirely from the market.

If you have experienced serious side effects as a result of taking Avandia/Rosiglitazone, a lawyer with experience in the ongoing Rosiglitazone litigation can help evaluate your claim at no charge. The Avandia recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Avandaryl®

dom — Thu, 22 Sep 2011 04:18:16 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY AVANDARYL, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Avandaryl (glimepiride and rosiglitazone) is a combination of two oral diabetes medicines that help control blood sugar levels.

Avandaryl is a form of drug that has been designed to help with treating diabetes. It helps with lowering and balancing your sugar levels especially in those who have type 2 diabetes. This drug should be taken along with having an exercise routine in play to help control levels of your blood’s sugar.

Uses of Avandaryl

Side Effects of Avandaryl

There are several side effects that patients may experience while taking this medication and can include:

Lawsuits

There are lawsuits against Avandaryl as there are some patients that claim they became injured after using this drug. There are many individual claims that are being filed and a patient wins the case if they can prove that there were injuries that were caused as a result of taking this medication.

Avandia has recently become more of a hot topic as the FDA has issued warnings based on the side effect of this medication. While there are benefits to those with type 2 diabetes, the side effects can be life threatening. There can be bone fractures as well as stroke which can do damage to an individual. Due to the side effects and the fact that they can be life threatening, the FDA over time may set a complete recall of this medication which will remove it entirely from the market.

If you have experienced serious side effects as a result of taking Avandaryl or Avandia, a lawyer with experience in the ongoing Avandaryl litigation can help evaluate your claim at no charge. The Avandia recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Avandamet®

dom — Thu, 22 Sep 2011 04:08:52 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY AVANDAMET, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Avandamet contains a combination of metformin and rosiglitazone, two oral diabetes medicines that help control blood sugar levels.

Avandamet is a form of drug that has been designed to help with treating diabetes. It helps with lowering and balancing your sugar levels especially in those who have type 2 diabetes. This drug should be taken along with having an exercise routine in play to help control levels of your blood’s sugar.

Uses of Avandamet

Side Effects of Avandamet

There are several side effects that patients may experience while taking this medication and can include:

Lawsuits

There are lawsuits against Avandamet as there are some patients that claim they became injured after using this drug. There are many individual claims that are being filed and a patient wins the case if they can prove that there were injuries that were caused as a result of taking this medication.

The drug Avandia has recently become more of a hot topic as the FDA has issued warnings based on the side effect of this medication. While there are benefits to those with type 2 diabetes, the side effects can be life threatening. There can be bone fractures as well as stroke which can do damage to an individual. Due to the side effects and the fact that they can be life threatening, the FDA over time may set a complete recall of this medication which will remove it entirely from the market.

If you have experienced serious side effects as a result of taking Avandamet or Avandia, a lawyer with experience in the ongoing Avandamet litigation can help evaluate your claim at no charge. The Avandia recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Avandia®

dom — Thu, 22 Sep 2011 03:59:25 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY AVANDIA, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Avandia can also be referred to as Rosiglitazone and is a form of drug that has been designed to help with treating diabetes. It helps with lowering and balancing your sugar levels especially in those who have type 2 diabetes. This drug should be taken along with having an exercise routine in play to help control levels of your blood’s sugar.

Uses of Avandia

Side Effects of Avandia

There are several side effects that patients may experience while taking this medication and can include:

Lawsuits

There are lawsuits against Avandia as there are some patients that claim they became injured after using this drug. There are many individual claims that are being filed and a patient wins the case if they can prove that there were injuries that were caused as a result of taking this medication. Also, the patient or doctor needs to inform Glaxo Smith of these effects and of their severity.

If you have experienced serious side effects as a result of taking Avandia, a lawyer with experience in the ongoing Avandia litigation can help evaluate your claim at no charge. The Avandia recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Di-Gesic®

dom — Sun, 18 Sep 2011 01:02:41 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY DI-GESIC, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Darvon (Dextropropoxyphene) is manufactured by Eli Lilly and Company. It is an analgesic in the opioid category and is intended to treat mild pain. In addition, it has an anti-tussive and local anesthetic effects. It has been taken off the market in Europe and the US due to concerns of fatal overdoses and arrhythmias. An estimated 10 million patients have used these products.

Dextropropoxyphene is sometimes combined with paracetamol or acetylsalicylic acid. Trade-names include Darvocet-N and Di-Gesic Darvon with APAP for dextropropoxyphene and paracetamol and Darvon with ASA for dextropropoxyphene and aspirin.

FDA ANNOUNCES DARVON RECALL: In November 2010, The US Food and Drug Administration announced a nationwide recall of this drug due to its use being linked to a high number of heart problems, as well as overdose and suicide.

DARVON (Darvocet) is reported to have caused serious injury to many thousands of users in the U.S. who have begun filing claims in the U.S. against Xanodyne Pharmaceutical seeking to recover financial compensation as a result of their suffering from heart attacks, strokes, heart rhythm abnormalities (arrhythmia) or other serious injuries and even deaths from the use of this drug.

This pain control medication, with properties similar to codeine, is an enormously popular drug used by millions in the treatment of mild to moderate pain. Also marketed as Darvocet, a compound containing both propoxyphene and acetaminophen, is one of the most popular pain relieving drugs in the U.S. The active medication–propoxyphene–relieves pain by acting on the central nervous system; however, its use has been linked over the years to thousands of deaths and serious injuries, most recently to potentially fatal heart rhythm abnormalities (arrhythmia).

DARVON (Darvocet) FDA BLACK BOX WARNING: The Food and Drug Administration has mandated that all DARVON (Darvocet) packages contain a black box label to warn consumers regarding the higher risks associated with consumption of these drugs.

Have you or a loved one suffered from any of the following serious side effects associated with Darvon (Darvocet), such as:

* Heart Attack
* Stroke
* Heart Arrythmia
* Suicide
* Overdose
* Death
* Any other serious side effects?

If the answer is yes, a lawyer with experience in the ongoing Di-Gesic litigation can help evaluate your claim at no charge. The Di-Gesic recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Dextropropoxyphene

dom — Sun, 18 Sep 2011 00:54:37 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY DEXTROPROPOXYPHENE, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Dextropropoxyphene is manufactured by Eli Lilly and Company. It is an analgesic in the opioid category and is intended to treat mild pain. In addition, it has an anti-tussive and local anesthetic effects. It has been taken off the market in Europe and the US due to concerns of fatal overdoses and arrhythmias. An estimated 10 million patients have used these products.

Dextropropoxyphene is sometimes combined with paracetamol or acetylsalicylic acid. Trade-names include Darvocet-N and Di-Gesic Darvon with APAP for dextropropoxyphene and paracetamol and Darvon with ASA for dextropropoxyphene and aspirin.

Have you or a loved one suffered from any of the following serious side effects associated with Darvon (Darvocet), such as:

* Heart Attack
* Stroke
* Heart Arrythmia
* Suicide
* Overdose
* Death
* Any other serious side effects?

If the answer is yes, a lawyer with experience in the ongoing Dextropropoxyphene litigation can help evaluate your claim at no charge. The Dextropropoxyphene recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Darvocet-N®

dom — Sun, 18 Sep 2011 00:44:06 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY DARVOCET-N, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

FDA ANNOUNCES DARVOCET RECALL: In November 2010, The US Food and Drug Administration announced a nationwide recall of this drug due to its use being linked to a high number of heart problems, as well as overdose and suicide.

DARVOCET (Darvon) is reported to have caused serious injury to many thousands of users in the U.S. who have begun filing claims in the U.S. against Xanodyne Pharmaceutical seeking to recover financial compensation as a result of their suffering from heart attacks, strokes, heart rhythm abnormalities (arrhythmia) or other serious injuries and even deaths from the use of this drug.

This pain control medication, with properties similar to codeine, is an enormously popular drug used by millions in the treatment of mild to moderate pain. Also marketed as Darvon, a compound containing both propoxyphene and acetaminophen, is one of the most popular pain relieving drugs in the U.S. The active medication–propoxyphene–relieves pain by acting on the central nervous system; however, its use has been linked over the years to thousands of deaths and serious injuries, most recently to potentially fatal heart rhythm abnormalities (arrhythmia).

DARVOCET (DARVON) FDA BLACK BOX WARNING: The Food and Drug Administration has mandated that all DARVOCET (Darvon) packages contain a black box label to warn consumers regarding the higher risks associated with consumption of these drugs.

Have you or a loved one suffered from any of the following serious side effects associated with Darvon (Darvocet), such as:

* Heart Attack
* Stroke
* Heart Arrythmia
* Suicide
* Overdose
* Death
* Any other serious side effects?

If the answer is yes, a lawyer with experience in the ongoing Darvocet (Darvon) litigation can help evaluate your claim at no charge. The Darvocetn recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Darvocet®

dom — Sun, 18 Sep 2011 00:35:49 +0000

If you have been a victim of Darvocet and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

This pain control medication, with properties similar to codeine, is an enormously popular drug used by millions in the treatment of mild to moderate pain. Also marketed as Darvon, a compound containing both propoxyphene and acetaminophen, is one of the most popular pain relieving drugs in the U.S. The active medication–propoxyphene–relieves pain by acting on the central nervous system; however, its use has been linked over the years to thousands of deaths and serious injuries, most recently to potentially fatal heart rhythm abnormalities (arrhythmia).

Have you or a loved one suffered from any of the following serious side effects associated with Darvon (Darvocet), such as:

* Heart Attack
* Stroke
* Heart Arrythmia
* Suicide
* Overdose
* Death
* Any other serious side effects?

Darvon®

dom — Sun, 18 Sep 2011 00:28:07 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY DARVON, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Have you or a loved one suffered from any of the following serious side effects associated with Darvon (Darvocet), such as:

* Heart Attack
* Stroke
* Heart Arrythmia
* Suicide
* Overdose
* Death
* Any other serious side effects?

If the answer is yes, a lawyer with experience in the ongoing Darvon (Darvocet) litigation can help evaluate your claim at no charge. The Darvon recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Nuvaring®

dom — Sun, 18 Sep 2011 00:18:48 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY NUVARING, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

NUVARING is a birth control device, used by over a million women worldwide. It was first approved for sale in the U.S. in 2002. It contains two hormones, progestrin and estrogen, that are released slowly from the ring to prevent pregnancy.

Since the birth control ring is a relatively new device, there are few studies to determine its safety or effectiveness. As early as 1995 reports surfaced of an increased risk of venous thrombosis (blood clots) in contraceptives such as this containing desogestrel compared to earlier “second generation” birth control pills. However, since then, it has been fraught with problems, as its use has been linked to almost half a dozen deaths, as well as a large number of life threatening blood clots, heart attacks, and strokes. The FDA has reported studies of increased risk of blood clots forming in the legs (Deep vein thrombosis or “DVT”), breaking off and traveling to the lungs where they may cause blockage (pulmonary embolism or” PE”).

NUVARING side effects may be the result in changes in your blood clotting system which some studies link to an increased risk of developing blood clots, strokes, and heart attacks with the type of progestin in NUVARING. Side effects should be immediately evaluated by a doctor because complications can cause serious injuries and be life-threatening.

NUVARING is reported to have caused serious injury to hundreds of women who have so far filed claims in the U.S. against Organon,Inc. seeking to recover financial compensation as a result of their suffering from blood clots, heart attacks, strokes, or other injuries from the use of NUVARING.

NUVARING FDA BLACK BOX WARNING: The Food and Drug Administration has mandated that all NUVARING packages contain a black box label to warn consumers regarding the higher risks associated with consumption of these drugs.

Have you or a loved one suffered from any of the following serious side effects associated with NUVARING, such as:

• Heart Attack
• Stroke
• Blood Clots in the Legs(DVT or Deep Vein Thrombosis)
• Blood Clots in the Lungs(PE or Pulmonary Embolism)
• Portal Vein Thrombosis
• Any other serious side effects?

If the answer is yes, a lawyer with experience in the ongoing NUVARING litigation can help evaluate your claim at no charge. The NUVARING attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form below.

Zyban®

dom — Sat, 17 Sep 2011 23:51:21 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ZYBAN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Zyban, in its generic form, is a drug used as a smoking cessation aid and as an antidepressant. It is different from typically prescribed antidepressants in that it isn’t a tricyclic. This drug inhibits norepinephrine-dopamine reuptake, but is also an antagonist of the nicotinic acetylcholine receptor, which is why it is has had much success as a stop smoking aid. In 2007, it was actually listed as number four for the most frequently prescribed antidepressants in the U.S. market.

Medical Uses of Zyban

Zyban has been used in the treatment of depression and it was found that those taking Zyban resulted in a lower overall weight. Zyban has also been used to accompany SSRIs when the SSRI was not effective as a first-line antidepressant. In fact, many reported feelings of increased energy, mood, motivation, cognitive function and sexual function.

Zyban was also used to treat anxiety and has been proven to be a successful option for adult ADHD; however, at higher dosage rates, it has the ability to cause agitation. In addition, the drug has been very successful at curbing the cravings and withdrawal symptoms of individuals that are trying to quit smoking. In studies, Zyban actually slowed the increase in weight that is typically associated with quitting smoking. Yet, after a period of 26 weeks, there was no effect, as both study groups showed an average weight gain of 4.8 kg.

Adverse Effects of Zyban

Zyban has many side effects associated with its use. Several minor side effects exist, but there are also some much more serious side effects associated with this drug. These more serious side effects are actually what caused the drug to be initially pulled off the market.

Zyban’s minor side effects are:
· Appetite changes
· Constipation
· Dizziness
· Dry mouth
· Increase in sweating
· Loss of sexual interest
· Migraines, headaches
· Nausea or vomiting
· Sleep issues

More serious side effects:
· Confusion or issues with concentration
· Fever
· Joint pain
· Hallucinations
· Convulsions or seizures (chances increase with alcohol use)
· Strange behavior or thoughts
· Rash, skin peeling or blistering
· Swollen glands
· Suicidal thoughts

Seizure risk was found to be dosage dependant, but at 2% risk for dosages of 600 mg compared to other drugs that top out at risks of 0.6%, there was obvious concern. Another side effect, hypertension, was noted in one study as severe for some patients.

Zyban also has the ability to cause birth defects. In fact, an eight year study ending in 2004 found that mothers giving birth to newborns afflicted with heart defects, more specifically left flow tract defects, had a higher likelihood of reporting that they had taken Zyban in the early part of their pregnancy. However, the evidence was not as specific as was needed, thus it was ruled that further studies were necessary. The FDA placed Zyban in the C pregnancy category, which means that a risk to the unborn child is present if this drug is taken during pregnancy.

If you have suffered a serious injury by taking Zyban, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Voxra®

dom — Sat, 17 Sep 2011 23:30:39 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY VOXRA, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Voxra, in its generic form, is a drug used as a smoking cessation aid and as an antidepressant. It is different from typically prescribed antidepressants in that it isn’t a tricyclic. This drug inhibits norepinephrine-dopamine reuptake, but is also an antagonist of the nicotinic acetylcholine receptor, which is why it is has had much success as a stop smoking aid. In 2007, it was actually listed as number four for the most frequently prescribed antidepressants in the U.S. market.

Medical Uses of Voxra

Voxra has been used in the treatment of depression and it was found that those taking Voxra resulted in a lower overall weight. Voxra has also been used to accompany SSRIs when the SSRI was not effective as a first-line antidepressant. In fact, many reported feelings of increased energy, mood, motivation, cognitive function and sexual function.

Voxra was also used to treat anxiety and has been proven to be a successful option for adult ADHD; however, at higher dosage rates, it has the ability to cause agitation. In addition, the drug has been very successful at curbing the cravings and withdrawal symptoms of individuals that are trying to quit smoking. In studies, Voxra actually slowed the increase in weight that is typically associated with quitting smoking. Yet, after a period of 26 weeks, there was no effect, as both study groups showed an average weight gain of 4.8 kg.

Adverse Effects of Voxra

Voxra has many side effects associated with its use. Several minor side effects exist, but there are also some much more serious side effects associated with this drug. These more serious side effects are actually what caused the drug to be initially pulled off the market.

Voxra’s minor side effects are:
· Appetite changes
· Constipation
· Dizziness
· Dry mouth
· Increase in sweating
· Loss of sexual interest
· Migraines, headaches
· Nausea or vomiting
· Sleep issues

Voxra also has the ability to cause birth defects. In fact, an eight year study ending in 2004 found that mothers giving birth to newborns afflicted with heart defects, more specifically left flow tract defects, had a higher likelihood of reporting that they had taken Voxra in the early part of their pregnancy. However, the evidence was not as specific as was needed, thus it was ruled that further studies were necessary. The FDA placed Voxra in the C pregnancy category, which means that a risk to the unborn child is present if this drug is taken during pregnancy.

If you have suffered a serious injury by taking Voxra, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Bupropion

dom — Sat, 17 Sep 2011 23:26:00 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY BUPROPION, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Bupropion, in its generic form, is a drug used as a smoking cessation aid and as an antidepressant. It is different from typically prescribed antidepressants in that it isn’t a tricyclic. This drug inhibits norepinephrine-dopamine reuptake, but is also an antagonist of the nicotinic acetylcholine receptor, which is why it is has had much success as a stop smoking aid. In 2007, it was actually listed as number four for the most frequently prescribed antidepressants in the U.S. market.

Medical Uses of Bupropion

Bupropion has been used in the treatment of depression and it was found that those taking Bupropion resulted in a lower overall weight. Bupropion has also been used to accompany SSRIs when the SSRI was not effective as a first-line antidepressant. In fact, many reported feelings of increased energy, mood, motivation, cognitive function and sexual function.

Bupropion was also used to treat anxiety and has been proven to be a successful option for adult ADHD; however, at higher dosage rates, it has the ability to cause agitation. In addition, the drug has been very successful at curbing the cravings and withdrawal symptoms of individuals that are trying to quit smoking. In studies, Bupropion actually slowed the increase in weight that is typically associated with quitting smoking. Yet, after a period of 26 weeks, there was no effect, as both study groups showed an average weight gain of 4.8 kg.

Adverse Effects of Bupropion

Bupropion has many side effects associated with its use. Several minor side effects exist, but there are also some much more serious side effects associated with this drug. These more serious side effects are actually what caused the drug to be initially pulled off the market.

Bupropion’s minor side effects are:
· Appetite changes
· Constipation
· Dizziness
· Dry mouth
· Increase in sweating
· Loss of sexual interest
· Migraines, headaches
· Nausea or vomiting
· Sleep issues

Bupropion also has the ability to cause birth defects. In fact, an eight year study ending in 2004 found that mothers giving birth to newborns afflicted with heart defects, more specifically left flow tract defects, had a higher likelihood of reporting that they had taken Bupropion in the early part of their pregnancy. However, the evidence was not as specific as was needed, thus it was ruled that further studies were necessary. The FDA placed Bupropion in the C pregnancy category, which means that a risk to the unborn child is present if this drug is taken during pregnancy.

If you have suffered a serious injury by taking Bupropion, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Budeprion®

dom — Sat, 17 Sep 2011 23:22:28 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY BUDEPRION, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Budeprion, or Bupropion in its generic form, is a drug used as a smoking cessation aid and as an antidepressant. It is different from typically prescribed antidepressants in that it isn’t a tricyclic. This drug inhibits norepinephrine-dopamine reuptake, but is also an antagonist of the nicotinic acetylcholine receptor, which is why it is has had much success as a stop smoking aid. In 2007, it was actually listed as number four for the most frequently prescribed antidepressants in the U.S. market.

Medical Uses of Budeprion

Budeprion has been used in the treatment of depression and it was found that those taking Budeprion resulted in a lower overall weight. Budeprion has also been used to accompany SSRIs when the SSRI was not effective as a first-line antidepressant. In fact, many reported feelings of increased energy, mood, motivation, cognitive function and sexual function.

Budeprion was also used to treat anxiety and has been proven to be a successful option for adult ADHD; however, at higher dosage rates, it has the ability to cause agitation. In addition, the drug has been very successful at curbing the cravings and withdrawal symptoms of individuals that are trying to quit smoking. In studies, Budeprion actually slowed the increase in weight that is typically associated with quitting smoking. Yet, after a period of 26 weeks, there was no effect, as both study groups showed an average weight gain of 4.8 kg.

Adverse Effects of Budeprion

Budeprion has many side effects associated with its use. Several minor side effects exist, but there are also some much more serious side effects associated with this drug. These more serious side effects are actually what caused the drug to be initially pulled off the market.

Budeprion’s minor side effects are:
· Appetite changes
· Constipation
· Dizziness
· Dry mouth
· Increase in sweating
· Loss of sexual interest
· Migraines, headaches
· Nausea or vomiting
· Sleep issues

Budeprion also has the ability to cause birth defects. In fact, an eight year study ending in 2004 found that mothers giving birth to newborns afflicted with heart defects, more specifically left flow tract defects, had a higher likelihood of reporting that they had taken Budeprion in the early part of their pregnancy. However, the evidence was not as specific as was needed, thus it was ruled that further studies were necessary. The FDA placed Budeprion in the C pregnancy category, which means that a risk to the unborn child is present if this drug is taken during pregnancy.

If you have suffered a serious injury by taking Budeprion, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Aplenzin®

dom — Sat, 17 Sep 2011 23:18:20 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY APLENZIN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Aplenzin, or Bupropion in its generic form, is a drug used as a smoking cessation aid and as an antidepressant. It is different from typically prescribed antidepressants in that it isn’t a tricyclic. This drug inhibits norepinephrine-dopamine reuptake, but is also an antagonist of the nicotinic acetylcholine receptor, which is why it is has had much success as a stop smoking aid. In 2007, it was actually listed as number four for the most frequently prescribed antidepressants in the U.S. market.

Medical Uses of Aplenzin

Aplenzin has been used in the treatment of depression and it was found that those taking Aplenzin resulted in a lower overall weight. Aplenzin has also been used to accompany SSRIs when the SSRI was not effective as a first-line antidepressant. In fact, many reported feelings of increased energy, mood, motivation, cognitive function and sexual function.

Aplenzin was also used to treat anxiety and has been proven to be a successful option for adult ADHD; however, at higher dosage rates, it has the ability to cause agitation. In addition, the drug has been very successful at curbing the cravings and withdrawal symptoms of individuals that are trying to quit smoking. In studies, Aplenzin actually slowed the increase in weight that is typically associated with quitting smoking. Yet, after a period of 26 weeks, there was no effect, as both study groups showed an average weight gain of 4.8 kg.

Adverse Effects of Aplenzin

Aplenzin has many side effects associated with its use. Several minor side effects exist, but there are also some much more serious side effects associated with this drug. These more serious side effects are actually what caused the drug to be initially pulled off the market.

Aplenzin’s minor side effects are:
· Appetite changes
· Constipation
· Dizziness
· Dry mouth
· Increase in sweating
· Loss of sexual interest
· Migraines, headaches
· Nausea or vomiting
· Sleep issues

Aplenzin also has the ability to cause birth defects. In fact, an eight year study ending in 2004 found that mothers giving birth to newborns afflicted with heart defects, more specifically left flow tract defects, had a higher likelihood of reporting that they had taken Aplenzin in the early part of their pregnancy. However, the evidence was not as specific as was needed, thus it was ruled that further studies were necessary. The FDA placed Aplenzin in the C pregnancy category, which means that a risk to the unborn child is present if this drug is taken during pregnancy.

If you have suffered a serious injury by taking Aplenzin, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Amfebutamone

dom — Sat, 17 Sep 2011 23:13:59 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY AMFEBUTAMONE, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Amfebutamone, or Bupropion in its generic form, is a drug used as a smoking cessation aid and as an antidepressant. It is different from typically prescribed antidepressants in that it isn’t a tricyclic. This drug inhibits norepinephrine-dopamine reuptake, but is also an antagonist of the nicotinic acetylcholine receptor, which is why it is has had much success as a stop smoking aid. In 2007, it was actually listed as number four for the most frequently prescribed antidepressants in the U.S. market.

Medical Uses of Amfebutamone

Amfebutamone has been used in the treatment of depression and it was found that those taking Amfebutamone resulted in a lower overall weight. Amfebutamone has also been used to accompany SSRIs when the SSRI was not effective as a first-line antidepressant. In fact, many reported feelings of increased energy, mood, motivation, cognitive function and sexual function.

Amfebutamone was also used to treat anxiety and has been proven to be a successful option for adult ADHD; however, at higher dosage rates, it has the ability to cause agitation. In addition, the drug has been very successful at curbing the cravings and withdrawal symptoms of individuals that are trying to quit smoking. In studies, Amfebutamone actually slowed the increase in weight that is typically associated with quitting smoking. Yet, after a period of 26 weeks, there was no effect, as both study groups showed an average weight gain of 4.8 kg.

Adverse Effects of Amfebutamone

Amfebutamone has many side effects associated with its use. Several minor side effects exist, but there are also some much more serious side effects associated with this drug. These more serious side effects are actually what caused the drug to be initially pulled off the market.

Amfebutamone’s minor side effects are:
· Appetite changes
· Constipation
· Dizziness
· Dry mouth
· Increase in sweating
· Loss of sexual interest
· Migraines, headaches
· Nausea or vomiting
· Sleep issues

Amfebutamone also has the ability to cause birth defects. In fact, an eight year study ending in 2004 found that mothers giving birth to newborns afflicted with heart defects, more specifically left flow tract defects, had a higher likelihood of reporting that they had taken Amfebutamone in the early part of their pregnancy. However, the evidence was not as specific as was needed, thus it was ruled that further studies were necessary. The FDA placed Amfebutamone in the C pregnancy category, which means that a risk to the unborn child is present if this drug is taken during pregnancy.

If you have suffered a serious injury by taking Amfebutamone, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Wellbutrin®

dom — Sat, 17 Sep 2011 23:08:40 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY WELLBUTRIN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Wellbutrin, or Bupropion in its generic form, is a drug used as a smoking cessation aid and as an antidepressant. It is different from typically prescribed antidepressants in that it isn’t a tricyclic. This drug inhibits norepinephrine-dopamine reuptake, but is also an antagonist of the nicotinic acetylcholine receptor, which is why it is has had much success as a stop smoking aid. In 2007, it was actually listed as number four for the most frequently prescribed antidepressants in the U.S. market.

Medical Uses of Wellbutrin

Wellbutrin has been used in the treatment of depression and it was found that those taking Wellbutrin resulted in a lower overall weight. Wellbutrin has also been used to accompany SSRIs when the SSRI was not effective as a first-line antidepressant. In fact, many reported feelings of increased energy, mood, motivation, cognitive function and sexual function.

Wellbutrin was also used to treat anxiety and has been proven to be a successful option for adult ADHD; however, at higher dosage rates, it has the ability to cause agitation. In addition, the drug has been very successful at curbing the cravings and withdrawal symptoms of individuals that are trying to quit smoking. In studies, Wellbutrin actually slowed the increase in weight that is typically associated with quitting smoking. Yet, after a period of 26 weeks, there was no effect, as both study groups showed an average weight gain of 4.8 kg.

Adverse Effects of Wellbutrin

Wellbutrin has many side effects associated with its use. Several minor side effects exist, but there are also some much more serious side effects associated with this drug. These more serious side effects are actually what caused the drug to be initially pulled off the market.

Wellbutrin’s minor side effects are:
· Appetite changes
· Constipation
· Dizziness
· Dry mouth
· Increase in sweating
· Loss of sexual interest
· Migraines, headaches
· Nausea or vomiting
· Sleep issues

Wellbutrin also has the ability to cause birth defects. In fact, an eight year study ending in 2004 found that mothers giving birth to newborns afflicted with heart defects, more specifically left flow tract defects, had a higher likelihood of reporting that they had taken Wellbutrin in the early part of their pregnancy. However, the evidence was not as specific as was needed, thus it was ruled that further studies were necessary. The FDA placed Wellbutrin in the C pregnancy category, which means that a risk to the unborn child is present if this drug is taken during pregnancy.

If you have suffered a serious injury by taking Wellbutrin, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Zypadhera®

dom — Sat, 17 Sep 2011 22:50:27 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ZYPADHERA, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Zypadhera is an antipsychotic drug used for the treatment of bipolar disorder and schizophrenia. Zypadhera is a generic form of the drug that is also marketed under the trade names Zolafren, Oferta, Olzapin and Zyprexa. Pharmaceutical giant Eli Lilly manufactures the blockbuster drug Zyprexa and the patent will expire in 2011. It was approved by the FDA for the treatment of manifestations of psychotic disorders, bipolar disorder depressive episodes and for long-term bipolar disorder treatment.

Common Forms and Dosage of Zypadhera

Zypadhera is available in three forms: tablets, disintegrating wafers and intramuscular injection. Tablets come in six dosage strengths ranging from 2.5 mg to 20 mg. Wafers range in strength from 5 mg to 20mg and intramuscular injections intended for short-term use come in 10 mg strength. The dosage depends upon the patient’s medical issues and drug response.

How Zypadhera Works in the Body

As with many of the atypical antipsychotics, Zypadhera affects the dopamine receptors and has a low affinity for alpha adrenergic, cholinergic muscarinic and histamine receptors. Zypadhera’s sedating properties may be contributed to by its weak affinity for the GABAA, BZD receptor area. Although Zypadhera’s mode of action on antipsychotic activity still isn’t known, it is possible that it involves antagonism at the serotonin receptors as well. However, antagonism at the dopamine receptors can cause extrapyramidal effects like tardive dyskinesia along with any therapeutic effects.

Side Effects of Zypadhera

Zypadhera, as with most antipsychotics, has a long list of side effects and adverse reactions. These include:

Minor Side Effects of Zalasta
· Dry Mouth
· Runny Nose
· Irritability
· Weight gain
· Increased appetite
· Constipation
· Missed periods
· Apathy

Major Side Effects
· Akathisia
· Sedation
· Insomnia
· Urinary retention
· Impaired judgment, motor skills and thinking
· Orthostatic hypotension
· Impaired spatial orientation
· Seizures
· Trouble swallowing
· Impaired spatial orientation
· Dental problems including teeth discoloration
· Difficulty regulating body temperature
· Brain Zaps
· Endocrine system side effects, including hyperglycemia, diabetes mellitus and hyperprolactinemia
· Auditory hallucinations

Diabetes has been a very serious concern in users of Zypadhera and for good reason. Zypadhera has been linked to a total of 288 cases of Zypadhera induced diabetes, which includes 23 deaths. In fact, the concern was so serious that the European Union and Japan both now require that Zypadhera labeling contain a diabetes warning.

Other than diabetes, hyperglycemia and ketoacidosis are also concerns. In fact, in nearly 50% of ketoacidosis reports caused by Zypadhera, the results are fatal.

Several lawsuits have been filed against Eli Lilly suggesting that the company has attempted to hide the dangers associated with their best selling drug for schizophrenia. The health risks associated with Zypadhera that have resulted in lawsuits are typically those that have resulted from the drug’s ability to cause diabetes. However, other lawsuits have been filed against the company for additional and equally serious side effects.

The drug itself is Eli Lilly’s most popular drug and, as of the time of this writing, sales of the drug were reportedly $4.2 billion the previous year.

If you have suffered a serious injury by taking Zypadhera, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Zolafren®

dom — Sat, 17 Sep 2011 22:43:39 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ZOLAFREN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Zolafren is an antipsychotic drug used for the treatment of bipolar disorder and schizophrenia. Zolafren is a generic form of the drug that is also marketed under the trade names Zypadhera, Oferta, Olzapin and Zyprexa. Pharmaceutical giant Eli Lilly manufactures the blockbuster drug Zyprexa and the patent will expire in 2011. It was approved by the FDA for the treatment of manifestations of psychotic disorders, bipolar disorder depressive episodes and for long-term bipolar disorder treatment.

Common Forms and Dosage of Zolafren

Zolafren is available in three forms: tablets, disintegrating wafers and intramuscular injection. Tablets come in six dosage strengths ranging from 2.5 mg to 20 mg. Wafers range in strength from 5 mg to 20mg and intramuscular injections intended for short-term use come in 10 mg strength. The dosage depends upon the patient’s medical issues and drug response.

How Zolafren Works in the Body

As with many of the atypical antipsychotics, Zolafren affects the dopamine receptors and has a low affinity for alpha adrenergic, cholinergic muscarinic and histamine receptors. Zolafren’s sedating properties may be contributed to by its weak affinity for the GABAA, BZD receptor area. Although Zolafren’s mode of action on antipsychotic activity still isn’t known, it is possible that it involves antagonism at the serotonin receptors as well. However, antagonism at the dopamine receptors can cause extrapyramidal effects like tardive dyskinesia along with any therapeutic effects.

Side Effects of Zolafren

Zolafren, as with most antipsychotics, has a long list of side effects and adverse reactions. These include:

Minor Side Effects of Zolafren
· Dry Mouth
· Runny Nose
· Irritability
· Weight gain
· Increased appetite
· Constipation
· Missed periods
· Apathy

Diabetes has been a very serious concern in users of Zolafren and for good reason. Zolafren has been linked to a total of 288 cases of Zolafren induced diabetes, which includes 23 deaths. In fact, the concern was so serious that the European Union and Japan both now require that Zolafren labeling contain a diabetes warning.

Other than diabetes, hyperglycemia and ketoacidosis are also concerns. In fact, in nearly 50% of ketoacidosis reports caused by Zolafren, the results are fatal.

Several lawsuits have been filed against Eli Lilly suggesting that the company has attempted to hide the dangers associated with their best selling drug for schizophrenia. The health risks associated with Zolafren that have resulted in lawsuits are typically those that have resulted from the drug’s ability to cause diabetes. However, other lawsuits have been filed against the company for additional and equally serious side effects.

The drug itself is Eli Lilly’s most popular drug and, as of the time of this writing, sales of the drug were reportedly $4.2 billion the previous year.

If you have suffered a serious injury by taking Zolafren, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Zalasta®

dom — Fri, 16 Sep 2011 17:18:16 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ZALASTA, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Zalasta is an antipsychotic drug used for the treatment of bipolar disorder and schizophrenia. Zalasta is a generic form of the drug that is also marketed under the trade names Zypadhera, Zolafren, Oferta and Olzapin. Pharmaceutical giant Eli Lilly manufactures the blockbuster drug Zyprexa and the patent will expire in 2011. It was approved by the FDA for the treatment of manifestations of psychotic disorders, bipolar disorder depressive episodes and for long-term bipolar disorder treatment.

Common Forms and Dosage of Zalasta

Zalasta is available in three forms: tablets, disintegrating wafers and intramuscular injection. Tablets come in six dosage strengths ranging from 2.5 mg to 20 mg. Wafers range in strength from 5 mg to 20mg and intramuscular injections intended for short-term use come in 10 mg strength. The dosage depends upon the patient’s medical issues and drug response.

How Zalasta Works in the Body

As with many of the atypical antipsychotics, Zalasta affects the dopamine receptors and has a low affinity for alpha adrenergic, cholinergic muscarinic and histamine receptors. Zalasta’s sedating properties may be contributed to by its weak affinity for the GABAA, BZD receptor area. Although Zalasta’s mode of action on antipsychotic activity still isn’t known, it is possible that it involves antagonism at the serotonin receptors as well. However, antagonism at the dopamine receptors can cause extrapyramidal effects like tardive dyskinesia along with any therapeutic effects.

Side Effects of Zalasta

Zalasta, as with most antipsychotics, has a long list of side effects and adverse reactions. These include:

Minor Side Effects of Zalasta
· Dry Mouth
· Runny Nose
· Irritability
· Weight gain
· Increased appetite
· Constipation
· Missed periods
· Apathy

Diabetes has been a very serious concern in users of Zalasta and for good reason. Zalasta has been linked to a total of 288 cases of Zalasta induced diabetes, which includes 23 deaths. In fact, the concern was so serious that the European Union and Japan both now require that Zalasta labeling contain a diabetes warning.

Other than diabetes, hyperglycemia and ketoacidosis are also concerns. In fact, in nearly 50% of ketoacidosis reports caused by Zalasta, the results are fatal.

Several lawsuits have been filed against Eli Lilly suggesting that the company has attempted to hide the dangers associated with their best selling drug for schizophrenia. The health risks associated with Zalasta that have resulted in lawsuits are typically those that have resulted from the drug’s ability to cause diabetes. However, other lawsuits have been filed against the company for additional and equally serious side effects.

The drug itself is Eli Lilly’s most popular drug and, as of the time of this writing, sales of the drug were reportedly $4.2 billion the previous year.

If you have suffered a serious injury by taking Zalasta, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Olzapin®

dom — Fri, 16 Sep 2011 16:56:02 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY OLZAPIN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Olzapin is an antipsychotic drug used for the treatment of bipolar disorder and schizophrenia. Olzapin is a generic form of the drug that is also marketed under the trade names Zalasta, Zypadhera, Zolafren, and Oferta. Pharmaceutical giant Eli Lilly manufactures the blockbuster drug Zyprexa and the patent will expire in 2011. It was approved by the FDA for the treatment of manifestations of psychotic disorders, bipolar disorder depressive episodes and for long-term bipolar disorder treatment.

Common Forms and Dosage of Olzapin

Olzapin is available in three forms: tablets, disintegrating wafers and intramuscular injection. Tablets come in six dosage strengths ranging from 2.5 mg to 20 mg. Wafers range in strength from 5 mg to 20mg and intramuscular injections intended for short-term use come in 10 mg strength. The dosage depends upon the patient’s medical issues and drug response.

How Olzapin Works in the Body

As with many of the atypical antipsychotics,Olzapin affects the dopamine receptors and has a low affinity for alpha adrenergic, cholinergic muscarinic and histamine receptors. Olzapin’s sedating properties may be contributed to by its weak affinity for the GABAA, BZD receptor area. Although Olzapin’s mode of action on antipsychotic activity still isn’t known, it is possible that it involves antagonism at the serotonin receptors as well. However, antagonism at the dopamine receptors can cause extrapyramidal effects like tardive dyskinesia along with any therapeutic effects.

Side Effects of Olzapin

Olzapin, as with most antipsychotics, has a long list of side effects and adverse reactions. These include:

Minor Side Effects of Olzapin
· Dry Mouth
· Runny Nose
· Irritability
· Weight gain
· Increased appetite
· Constipation
· Missed periods
· Apathy

Diabetes has been a very serious concern in users of Olzapin and for good reason. Olzapin has been linked to a total of 288 cases of Olzapin induced diabetes, which includes 23 deaths. In fact, the concern was so serious that the European Union and Japan both now require that Olzapin labeling contain a diabetes warning.

Other than diabetes, hyperglycemia and ketoacidosis are also concerns. In fact, in nearly 50% of ketoacidosis reports caused by Olzapin, the results are fatal.

Several lawsuits have been filed against Eli Lilly suggesting that the company has attempted to hide the dangers associated with their best selling drug for schizophrenia. The health risks associated with Olzapin that have resulted in lawsuits are typically those that have resulted from the drug’s ability to cause diabetes. However, other lawsuits have been filed against the company for additional and equally serious side effects.

Zyprexa is Eli Lilly’s most popular drug and, as of the time of this writing, sales of the drug were reportedly $4.2 billion the previous year.

If you have suffered a serious injury by taking Olzapin, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Olanzapine

dom — Fri, 16 Sep 2011 16:49:46 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY OLANZAPINE, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Olanzapine is an antipsychotic drug used for the treatment of bipolar disorder and schizophrenia. Olanzapine is a generic form of the drug that is also marketed under the trade names Zalasta, Zypadhera, Zolafren, Oferta and Olzapin. Pharmaceutical giant Eli Lilly manufactures the blockbuster drug Zyprexa and the patent will expire in 2011. It was approved by the FDA for the treatment of manifestations of psychotic disorders, bipolar disorder depressive episodes and for long-term bipolar disorder treatment.

Common Forms and Dosage of Olanzapine

Olanzapine is available in three forms: tablets, disintegrating wafers and intramuscular injection. Tablets come in six dosage strengths ranging from 2.5 mg to 20 mg. Wafers range in strength from 5 mg to 20mg and intramuscular injections intended for short-term use come in 10 mg strength. The dosage depends upon the patient’s medical issues and drug response.

How Olanzapine Works in the Body

As with many of the atypical antipsychotics, Olanzapine affects the dopamine receptors and has a low affinity for alpha adrenergic, cholinergic muscarinic and histamine receptors. Olanzapine’s sedating properties may be contributed to by its weak affinity for the GABAA, BZD receptor area. Although Olanzapine’s mode of action on antipsychotic activity still isn’t known, it is possible that it involves antagonism at the serotonin receptors as well. However, antagonism at the dopamine receptors can cause extrapyramidal effects like tardive dyskinesia along with any therapeutic effects.

Side Effects of Olanzapine

Olanzapine, as with most antipsychotics, has a long list of side effects and adverse reactions. These include:

Minor Side Effects of Olanzapine
· Dry Mouth
· Runny Nose
· Irritability
· Weight gain
· Increased appetite
· Constipation
· Missed periods
· Apathy

Diabetes has been a very serious concern in users of Olanzapine and for good reason. Olanzapine has been linked to a total of 288 cases of Olanzapine induced diabetes, which includes 23 deaths. In fact, the concern was so serious that the European Union and Japan both now require that Olanzapine labeling contain a diabetes warning.

Other than diabetes, hyperglycemia and ketoacidosis are also concerns. In fact, in nearly 50% of ketoacidosis reports caused by Zyprexa, the results are fatal.

Several lawsuits have been filed against Eli Lilly suggesting that the company has attempted to hide the dangers associated with their best selling drug for schizophrenia. The health risks associated with Olanzapine that have resulted in lawsuits are typically those that have resulted from the drug’s ability to cause diabetes. However, other lawsuits have been filed against the company for additional and equally serious side effects.

The drug itself is Eli Lilly’s most popular drug and, as of the time of this writing, sales of the drug were reportedly $4.2 billion the previous year.

If you have suffered a serious injury by taking Olanzapine, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Zyprexa®

dom — Fri, 16 Sep 2011 16:41:43 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ZYPREXA, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Zyprexa is an antipsychotic drug used for the treatment of bipolar disorder and schizophrenia. It is also known as Olanzapine (generic form) and under the trade names Zalasta, Zypadhera, Zolafren, Oferta and Olzapin. Pharmaceutical giant Eli Lilly manufactures the drug and the patent will expire in 2011. It was approved by the FDA for the treatment of manifestations of psychotic disorders, bipolar disorder depressive episodes and for long-term bipolar disorder treatment.

Common Forms and Dosage of Zyprexa

Zyprexa is available in three forms: tablets, disintegrating wafers and intramuscular injection. Tablets come in six dosage strengths ranging from 2.5 mg to 20 mg. Wafers range in strength from 5 mg to 20mg and intramuscular injections intended for short-term use come in 10 mg strength. The dosage
depends upon the patient’s medical issues and drug response.

How Zyprexa Works in the Body

As with many of the atypical antipsychotics, Zyprexa affects the dopamine receptors and has a low affinity for alpha adrenergic, cholinergic muscarinic and histamine receptors. Zyprexa’s sedating properties may be contributed to by its weak affinity for the GABAA, BZD receptor area. Although Zyprexa’s mode of action on antipsychotic activity still isn’t known, it is possible that it involves antagonism at the serotonin receptors as well. However, antagonism at the dopamine receptors can cause extrapyramidal effects like tardive dyskinesia along with any therapeutic effects.

Side Effects of Zyprexa

Zyprexa, as with most antipsychotics, has a long list of side effects and adverse reactions. These include:

Minor Side Effects of Zyprexa
· Dry Mouth
· Runny Nose
· Irritability
· Weight gain
· Increased appetite
· Constipation
· Missed periods
· Apathy

Diabetes has been a very serious concern in users of Zyprexa and for good reason. Zyprexa has been linked to a total of 288 cases of Zyprexa induced diabetes, which includes 23 deaths. In fact, the concern was so serious that the European Union and Japan both now require that Zyprexa labeling contain a diabetes warning.

Other than diabetes, hyperglycemia and ketoacidosis are also concerns. In fact, in nearly 50% of ketoacidosis reports caused by Zyprexa, the results are fatal.

Several lawsuits have been filed against Eli Lilly suggesting that the company has attempted to hide the dangers associated with their best selling drug for schizophrenia. The health risks associated with Zyprexa that have resulted in lawsuits are typically those that have resulted from the drug’s ability to cause diabetes. However, other lawsuits have been filed against the company for additional and equally serious side effects.

The drug itself is Eli Lilly’s most popular drug and, as of the time of this writing, sales of the drug were reportedly $4.2 billion the previous year.

If you have suffered a serious injury by taking Zyprexa, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Simvastatin

dom — Fri, 16 Sep 2011 16:22:20 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY SIMVASTATIN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Simvastatin falls into the statin pharmaceutical class and is a hypolipidemic drug that is frequently used in cholesterol control and hypercholesterolemia.

Simvastatin is the name of the drug in generic form. The drug has also been used to increase HDLs and lower triglyceride levels. It is possible that Zocor might actually inhibit atherosclerosis progression, but this is still being studied. Current theories suggest that this may be due to the effect that Simvastatin has on macrophages present in lesions of atherosclerotic plaque. It has further been suggested that patients with more than one cardiovascular disease risk factor may possibly benefit from statins like Simlup even if their cholesterol levels are not yet elevated.

Common Adverse Effects of Simvastatin

Like all pharmaceuticals, Simvastatin can have adverse effects. The most common of which are:

· Diarrhea
· Weakness
· Indigestion
· Abdominal Pain
· Hives
· Itching
· Fatigue
· Fever
· Rashes

More Serious Adverse Effects of Simvastatin

Simvastatin also has some more serious side effects associated with its use. These adverse reactions include:

· Muscle cramps
· Memory loss
· Joint pain
· Hepatic cirrhosis
· Myositis
· Cholestatic hepatitis
· Rhabdomyolysis
· Chest pain
· Yellow skin
· Swollen skin
· Yellow eyes
· Peeling skin
· Dark urine
· Pale stool

Simvastatin Dosage and Interactions

Simvastatin is available in dosages of 5 mg to as high as 80 mg. Simvastatin also has the ability to negatively interact with certain foods and other commonly prescribed medications. These include:

· Graprefruit – Individuals taking Simvastatin should refrain from eating grapefruit and other grapefruit products or drinking grapefruit juice because this will slow the matabolization of Simlup and cause toxicity risks.

· Amiodarone – Patients taking more than 20 mg of Simcard per day should refrain from using the drug in combination with Amiodarone, as this combination has a high risk of causing rhabdomyolysis. This condition can cause kidney failure and even death.

· Myopathy can occur in patients with high dosage rates (80 mg) at an estimated rate of 61 of 1,000 patients. Myopathy is essentially muscle injury or damage. Even smaller doses (40 mg) can cause myopathy; however, the occurrence is remarkably lower at 8 of 10,000 patients.

· Patients currently taking Clarithromycin, Erythromycin, Itraconazole, Ketoconazole, Nefazodone, Telithromycin and HIV protease inhibitors should not take Simcard in combination with these medications.

· Patients currently on a dosage of 10 mg of Simvastatin should not combine it with Cyclosporine, Danazol or Gemfibrozil.

· Patients taking 20 mg of Simvastatin should refrain from combining it with Verapamil.

· Patients taking 40 mg of Simvastatin should refrain from combining it with Diltiazem.

Merck is the maker of Zocor; however, the patent expired in June of 2006. Merck made a smart move at that time, choosing to reduce the price in order to remain competitive with companies offering generic forms of the drug. The result was that Merck was able to remain a key player in the game. In fact, two of the main health insurance companies in the United States, WellPoint and UnitedHealthcare, actually provide Simvastatin to members for the price of a generic copay drug.

If you have suffered a serious injury by taking Simvastatin, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Simvacor®

dom — Fri, 16 Sep 2011 16:18:22 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY SIMVACOR, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Simvacor falls into the statin pharmaceutical class and is a hypolipidemic drug that is frequently used in cholesterol control and hypercholesterolemia.

Also known as Simvastatin in generic form, this drug has also been used to increase HDLs and lower triglyceride levels. It is possible that Zocor might actually inhibit atherosclerosis progression, but this is still being studied. Current theories suggest that this may be due to the effect that Simvacor has on macrophages present in lesions of atherosclerotic plaque. It has further been suggested that patients with more than one cardiovascular disease risk factor may possibly benefit from statins like Simlup even if their cholesterol levels are not yet elevated.

Common Adverse Effects of Simvacor

Like all pharmaceuticals, Simvacor can have adverse effects. The most common of which are:

· Diarrhea
· Weakness
· Indigestion
· Abdominal Pain
· Hives
· Itching
· Fatigue
· Fever
· Rashes

More Serious Adverse Effects of Simvacor

Simvacor also has some more serious side effects associated with its use. These adverse reactions include:

Simvacor Dosage and Interactions

Simvacor is available in dosages of 5 mg to as high as 80 mg. Simvacor also has the ability to negatively interact with certain foods and other commonly prescribed medications. These include:

· Graprefruit – Individuals taking Simvacor should refrain from eating grapefruit and other grapefruit products or drinking grapefruit juice because this will slow the matabolization of Simlup and cause toxicity risks.

· Patients currently on a dosage of 10 mg of Simvacor should not combine it with Cyclosporine, Danazol or Gemfibrozil.

· Patients taking 20 mg of Simvacor should refrain from combining it with Verapamil.

· Patients taking 40 mg of Simvacor should refrain from combining it with Diltiazem.

Merck is the maker of Zocor; however, the patent expired in June of 2006. Merck made a smart move at that time, choosing to reduce the price in order to remain competitive with companies offering generic forms of the drug. The result was that Merck was able to remain a key player in the game. In fact, two of the main health insurance companies in the United States, WellPoint and UnitedHealthcare, actually provide Simvacor to members for the price of a generic copay drug.

If you have suffered a serious injury by taking Simvacor, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Simlup®

dom — Fri, 16 Sep 2011 16:14:17 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY SIMLUP, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Simlup falls into the statin pharmaceutical class and is a hypolipidemic drug that is frequently used in cholesterol control and hypercholesterolemia.

Also known as Simvastatin in generic form, this drug has also been used to increase HDLs and lower triglyceride levels. It is possible that Zocor might actually inhibit atherosclerosis progression, but this is still being studied. Current theories suggest that this may be due to the effect that Simlup has on macrophages present in lesions of atherosclerotic plaque. It has further been suggested that patients with more than one cardiovascular disease risk factor may possibly benefit from statins like Simlup even if their cholesterol levels are not yet elevated.

Common Adverse Effects of Simlup

Like all pharmaceuticals, Simlup can have adverse effects. The most common of which are:

· Diarrhea
· Weakness
· Indigestion
· Abdominal Pain
· Hives
· Itching
· Fatigue
· Fever
· Rashes

More Serious Adverse Effects of Simlup

Simlup also has some more serious side effects associated with its use. These adverse reactions include:

Simlup Dosage and Interactions

Simlup is available in dosages of 5 mg to as high as 80 mg. Simlup also has the ability to negatively interact with certain foods and other commonly prescribed medications. These include:

· Graprefruit – Individuals taking Simlup should refrain from eating grapefruit and other grapefruit products or drinking grapefruit juice because this will slow the matabolization of Simlup and cause toxicity risks.

· Patients currently on a dosage of 10 mg of Simlup should not combine it with Cyclosporine, Danazol or Gemfibrozil.

· Patients taking 20 mg of Simlup should refrain from combining it with Verapamil.

· Patients taking 40 mg of Simlup should refrain from combining it with Diltiazem.

Merck is the maker of Zocor; however, the patent expired in June of 2006. Merck made a smart move at that time, choosing to reduce the price in order to remain competitive with companies offering generic forms of the drug. The result was that Merck was able to remain a key player in the game. In fact, two of the main health insurance companies in the United States, WellPoint and UnitedHealthcare, actually provide Simcard to members for the price of a generic copay drug.

If you have suffered a serious injury by taking Simlup, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Simcard®

dom — Fri, 16 Sep 2011 16:08:06 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY SIMCARD, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Simcard falls into the statin pharmaceutical class and is a hypolipidemic drug that is frequently used in cholesterol control and hypercholesterolemia.

Also known as Simvastatin in generic form, this drug has also been used to increase HDLs and lower triglyceride levels. It is possible that Zocor might actually inhibit atherosclerosis progression, but this is still being studied. Current theories suggest that this may be due to the effect that Simcard has on macrophages present in lesions of atherosclerotic plaque. It has further been suggested that patients with more than one cardiovascular disease risk factor may possibly benefit from statins like Simcard even if their cholesterol levels are not yet elevated.

Common Adverse Effects of Simcard

Like all pharmaceuticals, Simcard can have adverse effects. The most common of which are:

· Diarrhea
· Weakness
· Indigestion
· Abdominal Pain
· Hives
· Itching
· Fatigue
· Fever
· Rashes

More Serious Adverse Effects of Simcard

Simcard also has some more serious side effects associated with its use. These adverse reactions include:

Simcard Dosage and Interactions

Simcard is available in dosages of 5 mg to as high as 80 mg. Simcard also has the ability to negatively interact with certain foods and other commonly prescribed medications. These include:

· Graprefruit – Individuals taking Simcard should refrain from eating grapefruit and other grapefruit products or drinking grapefruit juice because this will slow the matabolization of Simcard and cause toxicity risks.

· Patients currently on a dosage of 10 mg of Simcard should not combine it with Cyclosporine, Danazol or Gemfibrozil.

· Patients taking 20 mg of Simcard should refrain from combining it with Verapamil.

· Patients taking 40 mg of Simcard should refrain from combining it with Diltiazem.

Merck is the maker of Zocor; however, the patent expired in June of 2006. Merck made a smart move at that time, choosing to reduce the price in order to remain competitive with companies offering generic forms of the drug. The result was that Merck was able to remain a key player in the game. In fact, two of the main health insurance companies in the United States, WellPoint and UnitedHealthcare, actually provide Simcard to members for the price of a generic copay drug.

If you have suffered a serious injury by taking Simcard, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Metoclopramide

dom — Fri, 16 Sep 2011 00:12:54 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY METOCLOPRAMIDE, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Metoclopramide is what is known as a gastroprokinetic agent and antiemetic. The drug is frequently used in the treatment of vomiting or nausea and is often prescribed for patients suffering from gastroparesis to assist with gastric emptying. It has also been used to treat migraines.

If you have been a victim of Metoclopramide (marketed under the following trade names: Reglan, Cerucal, Degan, Maxeran, Maxolon, Metoclopramide, Pramin, Primperan, Pylomid) and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Metoclopramide has been given to treat the nausea and subsequent vomiting that is associated with morphine use, uremia, malignancy, infection, labor, migraines and radiation sickness. It has also been used in combination with acetaminophen or aspirin. Unfortunately, Metoclopramide has proved to be ineffective in relieving nausea due to motion sickness, chemotherapy and postoperative nausea.

Metoclopramide has also been used to inhibit dopamine’s action and stimulate lactation in mothers that are having trouble producing a suitable amount of milk for their breastfeeding infant.

Adverse Effects of Metoclopramide

Women in every stage of pregnancy have used Metoclopramide without issue to the unborn child or mother. The drug is excreted in the mother’s milk. However, Metoclopramide does have several adverse effects associated with its use, most of which occur after long-term use. Some of the more common side effects are listed below:

Metoclopramide has also been associated with some more serious side effects, including:

Any individual developing any of these serious complications while taking Metoclopramide should immediately seek medical care and be sure to complete any prescribed treatments in order to achieve the best chance possible of recovery. Unfortunately, some of the more serious side effects of Metoclopramide can be chronic and permanent, resulting in many previous Metoclopramide users choosing to file suit against the manufacturer.

The FDA suggests that drugs like Metoclopramide only be used as a short term option, preferably under 12 weeks. This is due to the reports that tardive dyskinesia frequently occurs in patients using the drug in excess of three months. This same concern eventually influenced the FDA to require that all metoclopramide manufacturers issue black box warnings for the side effect tardive dyskinesia, noting that this occurs with high dosage or chronic use.

Metoclopramide should not be taken in cases of phaeochromocytoma or a bowel obstruction. In addition, in patients with Parkinson’s disease it should be avoided or used cautiously. The same is true for those suffering from clinical depression because the drug can actually worsen the patient’s mental state with long-term use.

If you have suffered a serious injury by taking Metoclopramide, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Pylomid®

dom — Fri, 16 Sep 2011 00:05:09 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY PYLOMID, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Pylomid, also known as Metoclopramide, is what is known as a gastroprokinetic agent and antiemetic. The drug is frequently used in the treatment of vomiting or nausea and is often prescribed for patients suffering from gastroparesis to assist with gastric emptying. It has also been used to treat migraines.

If you have been a victim of Pylomid and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Pylomid has been given to treat the nausea and subsequent vomiting that is associated with morphine use, uremia, malignancy, infection, labor, migraines and radiation sickness. It has also been used in combination with acetaminophen or aspirin. Unfortunately, Pylomid has proved to be ineffective in relieving nausea due to motion sickness, chemotherapy and postoperative nausea.

Pylomid has also been used to inhibit dopamine’s action and stimulate lactation in mothers that are having trouble producing a suitable amount of milk for their breastfeeding infant.

Adverse Effects of Pylomid

Women in every stage of pregnancy have used Pylomid without issue to the unborn child or mother. The drug is excreted in the mother’s milk. However, Pylomid does have several adverse effects associated with its use, most of which occur after long-term use. Some of the more common side effects are listed below:

Pylomid has also been associated with some more serious side effects, including:

Any individual developing any of these serious complications while taking Pylomid should immediately seek medical care and be sure to complete any prescribed treatments in order to achieve the best chance possible of recovery. Unfortunately, some of the more serious side effects of Pylomid can be chronic and permanent, resulting in many previous Pylomid users choosing to file suit against the manufacturer.

The FDA suggests that drugs like Pylomid or Reglan only be used as a short term option, preferably under 12 weeks. This is due to the reports that tardive dyskinesia frequently occurs in patients using the drug in excess of three months. This same concern eventually influenced the FDA to require that all metoclopramide manufacturers issue black box warnings for the side effect tardive dyskinesia, noting that this occurs with high dosage or chronic use.

Pylomid should not be taken in cases of phaeochromocytoma or a bowel obstruction. In addition, in patients with Parkinson’s disease it should be avoided or used cautiously. The same is true for those suffering from clinical depression because the drug can actually worsen the patient’s mental state with long-term use.

If you have suffered a serious injury by taking Pylomid, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Primperan®

dom — Thu, 15 Sep 2011 23:51:16 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY PRIMPERAN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Primperan, also known as Metoclopramide, is what is known as a gastroprokinetic agent and antiemetic. The drug is frequently used in the treatment of vomiting or nausea and is often prescribed for patients suffering from gastroparesis to assist with gastric emptying. It has also been used to treat migraines.

If you have been a victim of Primperan and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Primperan has been given to treat the nausea and subsequent vomiting that is associated with morphine use, uremia, malignancy, infection, labor, migraines and radiation sickness. It has also been used in combination with acetaminophen or aspirin. Unfortunately, Primperan has proved to be ineffective in relieving nausea due to motion sickness, chemotherapy and postoperative nausea.

Primperan has also been used to inhibit dopamine’s action and stimulate lactation in mothers that are having trouble producing a suitable amount of milk for their breastfeeding infant.

Adverse Effects of Primperan

Women in every stage of pregnancy have used Primperan without issue to the unborn child or mother. The drug is excreted in the mother’s milk. However, Pramin does have several adverse effects associated with its use, most of which occur after long-term use. Some of the more common side effects are listed below:

Primperan has also been associated with some more serious side effects, including:

Any individual developing any of these serious complications while taking Primperan should immediately seek medical care and be sure to complete any prescribed treatments in order to achieve the best chance possible of recovery. Unfortunately, some of the more serious side effects of Primperan can be chronic and permanent, resulting in many previous Primperan users choosing to file suit against the manufacturer.

The FDA suggests that drugs like Primperan or Reglan only be used as a short term option, preferably under 12 weeks. This is due to the reports that tardive dyskinesia frequently occurs in patients using the drug in excess of three months. This same concern eventually influenced the FDA to require that all metoclopramide manufacturers issue black box warnings for the side effect tardive dyskinesia, noting that this occurs with high dosage or chronic use.

Primperan should not be taken in cases of phaeochromocytoma or a bowel obstruction. In addition, in patients with Parkinson’s disease it should be avoided or used cautiously. The same is true for those suffering from clinical depression because the drug can actually worsen the patient’s mental state with long-term use.

The drug Reglan is produced by pharmaceutical manufacturer Schwarz Pharma; however, it is known generically as metoclopramide and has been sold under several different brand names. These include: Degan, which is made by the manufacturer Lek; Primperan and Maxeran, both made by pharmaceutical company Sanofi Aventis; Maxolon, made by manufacturer Shire/Valeant; and Pylomid, made by a company called Bosnalijek.

If you have suffered a serious injury by taking Primperan, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Maxolon®

dom — Thu, 15 Sep 2011 23:38:19 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY MAXOLON, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Maxolon, also known as Metoclopramide, is what is known as a gastroprokinetic agent and antiemetic. The drug is frequently used in the treatment of vomiting or nausea and is often prescribed for patients suffering from gastroparesis to assist with gastric emptying. It has also been used to treat migraines.

If you have been a victim of Maxolon and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Maxolon has been given to treat the nausea and subsequent vomiting that is associated with morphine use, uremia, malignancy, infection, labor, migraines and radiation sickness. It has also been used in combination with acetaminophen or aspirin. Unfortunately, Maxolon has proved to be ineffective in relieving nausea due to motion sickness, chemotherapy and postoperative nausea.

Maxolon has also been used to inhibit dopamine’s action and stimulate lactation in mothers that are having trouble producing a suitable amount of milk for their breastfeeding infant.

Adverse Effects of Maxolon

Women in every stage of pregnancy have used Maxolon without issue to the unborn child or mother. The drug is excreted in the mother’s milk. However, Maxolon does have several adverse effects associated with its use, most of which occur after long-term use. Some of the more common side effects are listed below:

Maxolon has also been associated with some more serious side effects, including:

Any individual developing any of these serious complications while taking Maxolon should immediately seek medical care and be sure to complete any prescribed treatments in order to achieve the best chance possible of recovery. Unfortunately, some of the more serious side effects of Maxolon can be chronic and permanent, resulting in many previous Maxolon users choosing to file suit against the manufacturer.

The FDA suggests that drugs like Maxolon or Reglan only be used as a short term option, preferably under 12 weeks. This is due to the reports that tardive dyskinesia frequently occurs in patients using the drug in excess of three months. This same concern eventually influenced the FDA to require that all metoclopramide manufacturers issue black box warnings for the side effect tardive dyskinesia, noting that this occurs with high dosage or chronic use.

Maxolon should not be taken in cases of phaeochromocytoma or a bowel obstruction. In addition, in patients with Parkinson’s disease it should be avoided or used cautiously. The same is true for those suffering from clinical depression because the drug can actually worsen the patient’s mental state with long-term use.

The drug Reglan is produced by pharmaceutical manufacturer Schwarz Pharma; however, it is known generically as metoclopramide and has been sold under several different brand names. These include: Degan, which is made by the manufacturer Lek; Primperan and Maxeran, both made by pharmaceutical company Sanofi Aventis; Maxolon, made by manufacturer Shire/Valeant; and Pylomid, made by a company called Bosnalijek.

If you have suffered a serious injury by taking Maxolon, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Maxeran®

dom — Thu, 15 Sep 2011 23:33:31 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY MAXERAN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Maxeran, also known as Metoclopramide, is what is known as a gastroprokinetic agent and antiemetic. The drug is frequently used in the treatment of vomiting or nausea and is often prescribed for patients suffering from gastroparesis to assist with gastric emptying. It has also been used to treat migraines.

If you have been a victim of Maxeran and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Maxeran has been given to treat the nausea and subsequent vomiting that is associated with morphine use, uremia, malignancy, infection, labor, migraines and radiation sickness. It has also been used in combination with acetaminophen or aspirin. Unfortunately, Maxeran has proved to be ineffective in relieving nausea due to motion sickness, chemotherapy and postoperative nausea.

Maxeran has also been used to inhibit dopamine’s action and stimulate lactation in mothers that are having trouble producing a suitable amount of milk for their breastfeeding infant.

Adverse Effects of Maxeran

Women in every stage of pregnancy have used Maxeran without issue to the unborn child or mother. The drug is excreted in the mother’s milk. However, Maxeran does have several adverse effects associated with its use, most of which occur after long-term use. Some of the more common side effects are listed below:

Maxeran has also been associated with some more serious side effects, including:

Any individual developing any of these serious complications while taking Maxeran should immediately seek medical care and be sure to complete any prescribed treatments in order to achieve the best chance possible of recovery. Unfortunately, some of the more serious side effects of Maxeran can be chronic and permanent, resulting in many previous Maxeran users choosing to file suit against the manufacturer.

The FDA suggests that drugs like Maxeran or Reglan only be used as a short term option, preferably under 12 weeks. This is due to the reports that tardive dyskinesia frequently occurs in patients using the drug in excess of three months. This same concern eventually influenced the FDA to require that all metoclopramide manufacturers issue black box warnings for the side effect tardive dyskinesia, noting that this occurs with high dosage or chronic use.

Maxeran should not be taken in cases of phaeochromocytoma or a bowel obstruction. In addition, in patients with Parkinson’s disease it should be avoided or used cautiously. The same is true for those suffering from clinical depression because the drug can actually worsen the patient’s mental state with long-term use.

If you have suffered a serious injury by taking Maxeran, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Degan®

dom — Thu, 15 Sep 2011 23:25:50 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY DEGAN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Degan, also known as Metoclopramide, is what is known as a gastroprokinetic agent and antiemetic. The drug is frequently used in the treatment of vomiting or nausea and is often prescribed for patients suffering from gastroparesis to assist with gastric emptying. It has also been used to treat migraines.

If you have been a victim of Degan and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Degan has been given to treat the nausea and subsequent vomiting that is associated with morphine use, uremia, malignancy, infection, labor, migraines and radiation sickness. It has also been used in combination with acetaminophen or aspirin. Unfortunately, Degan has proved to be ineffective in relieving nausea due to motion sickness, chemotherapy and postoperative nausea.

Degan has also been used to inhibit dopamine’s action and stimulate lactation in mothers that are having trouble producing a suitable amount of milk for their breastfeeding infant.

Adverse Effects of Degan

Women in every stage of pregnancy have used Degan without issue to the unborn child or mother. The drug is excreted in the mother’s milk. However, Degan does have several adverse effects associated with its use, most of which occur after long-term use. Some of the more common side effects are listed below:

Degan has also been associated with some more serious side effects, including:

Any individual developing any of these serious complications while taking Degan should immediately seek medical care and be sure to complete any prescribed treatments in order to achieve the best chance possible of recovery. Unfortunately, some of the more serious side effects of Degan can be chronic and permanent, resulting in many previous Degan users choosing to file suit against the manufacturer.

The FDA suggests that drugs like Degan or Reglan only be used as a short term option, preferably under 12 weeks. This is due to the reports that tardive dyskinesia frequently occurs in patients using the drug in excess of three months. This same concern eventually influenced the FDA to require that all metoclopramide manufacturers issue black box warnings for the side effect tardive dyskinesia, noting that this occurs with high dosage or chronic use.

Degan should not be taken in cases of phaeochromocytoma or a bowel obstruction. In addition, in patients with Parkinson’s disease it should be avoided or used cautiously. The same is true for those suffering from clinical depression because the drug can actually worsen the patient’s mental state with long-term use.

The drug Reglan is produced by pharmaceutical manufacturer Schwarz Pharma; however, it is known generically as metoclopramide and has been sold under several different brand names. These include: Degan, which is made by the manufacturer Lek; Primperan and Maxeran, both made by pharmaceutical company Sanofi Aventis; Maxolon, made by manufacturer Shire/Valeant; and Pylomid, made by a company called Bosnalijek.

If you have suffered a serious injury by taking Degan, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Cerucal®

dom — Thu, 15 Sep 2011 23:11:59 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY CERUCAL, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Cerucal, also known as Metoclopramide, is what is known as a gastroprokinetic agent and antiemetic. The drug is frequently used in the treatment of vomiting or nausea and is often prescribed for patients suffering from gastroparesis to assist with gastric emptying. It has also been used to treat migraines.

If you have been a victim of Cerucal and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Cerucal has been given to treat the nausea and subsequent vomiting that is associated with morphine use, uremia, malignancy, infection, labor, migraines and radiation sickness. It has also been used in combination with acetaminophen or aspirin. Unfortunately, Reglan has proved to be ineffective in relieving nausea due to motion sickness, chemotherapy and postoperative nausea.

Reglan has also been used to inhibit dopamine’s action and stimulate lactation in mothers that are having trouble producing a suitable amount of milk for their breastfeeding infant.

Adverse Effects of Cerucal

Women in every stage of pregnancy have used Cerucal without issue to the unborn child or mother. The drug is excreted in the mother’s milk. However, Cerucal does have several adverse effects associated with its use, most of which occur after long-term use. Some of the more common side effects are listed below:

Cerucal has also been associated with some more serious side effects, including:

Any individual developing any of these serious complications while taking Cerucal should immediately seek medical care and be sure to complete any prescribed treatments in order to achieve the best chance possible of recovery. Unfortunately, some of the more serious side effects of Cerucal can be chronic and permanent, resulting in many previous Cerucal users choosing to file suit against the manufacturer.

The FDA suggests that drugs like Cerucal or Reglan only be used as a short term option, preferably under 12 weeks. This is due to the reports that tardive dyskinesia frequently occurs in patients using the drug in excess of three months. This same concern eventually influenced the FDA to require that all metoclopramide manufacturers issue black box warnings for the side effect tardive dyskinesia, noting that this occurs with high dosage or chronic use.

Cerucal should not be taken in cases of phaeochromocytoma or a bowel obstruction. In addition, in patients with Parkinson’s disease it should be avoided or used cautiously. The same is true for those suffering from clinical depression because the drug can actually worsen the patient’s mental state with long-term use.

If you have suffered a serious injury by taking Cerucal, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Reglan®

dom — Thu, 15 Sep 2011 22:55:25 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY REGLAN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Reglan, also known as Metoclopramide, is what is known as a gastroprokinetic agent and antiemetic. The drug is frequently used in the treatment of vomiting or nausea and is often prescribed for patients suffering from gastroparesis to assist with gastric emptying. It has also been used to treat migraines.

If you have been a victim of Reglan and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Reglan has been given to treat the nausea and subsequent vomiting that is associated with morphine use, uremia, malignancy, infection, labor, migraines and radiation sickness. It has also been used in combination with acetaminophen or aspirin. Unfortunately, Reglan has proved to be ineffective in
relieving nausea due to motion sickness, chemotherapy and postoperative nausea.

Reglan has also been used to inhibit dopamine’s action and stimulate lactation in mothers that are having trouble producing a suitable amount of milk for their breastfeeding infant.

Adverse Effects of Reglan

Women in every stage of pregnancy have used Reglan without issue to the unborn child or mother. The drug is excreted in the mother’s milk. However, Reglan does have several adverse effects associated with its use, most of which occur after long-term use. Some of the more common side effects are listed below:

Reglan has also been associated with some more serious side effects, including:

Any individual developing any of these serious complications while taking Reglan should immediately seek medical care and be sure to complete any prescribed treatments in order to achieve the best chance possible of recovery. Unfortunately, some of the more serious side effects of Reglan can be
chronic and permanent, resulting in many previous Reglan users choosing to file suit against the manufacturer.

The FDA suggests that Reglan only be used as a short term option, preferably under 12 weeks. This is due to the reports that tardive dyskinesia frequently occurs in patients using the drug in excess of three months. This same concern eventually influenced the FDA to require that all metoclopramide manufacturers issue black box warnings for the side effect tardive dyskinesia, noting that this occurs with high dosage or chronic use.

Reglan should not be taken in cases of phaeochromocytoma or a bowel obstruction. In addition, in patients with Parkinson’s disease it should be avoided or used cautiously. The same is true for those suffering from clinical depression because the drug can actually worsen the patient’s mental state with long-term use.

Reglan is produced by pharmaceutical manufacturer, Schwarz Pharma; however, it is known generically as metoclopramide and has been sold under several different brand names. These include: Degan, which is made by the manufacturer Lek; Primperan and Maxeran, both made by pharmaceutical company Sanofi Aventis; Maxolon, made by manufacturer Shire/Valeant; and Pylomid, made by a company called Bosnalijek.

If you have suffered a serious injury by taking Reglan, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Simply Thick

dom — Thu, 15 Sep 2011 16:45:32 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY SIMPLY THICK, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Following an FDA warning, a recall has been issued by Simply Thick, LLC of its “Simply Thick” infant formula/breast milk thickening agent. Simply Thick gel is mixed with breast milk or formula, and often fed to premature infants as part of a feeding program to assist them in swallowing.

If you have been a victim of this product and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

A substantial and growing number of lawsuits have now been filed throughout the U.S. by the families of critically injured infants who allegedly suffered from a life threatening condition known as necrotizing enterocolitis (NEC) from the ingestion of the Simply Thick thickening gel. The potentially deadly NEC condition is often characterized by symptoms such as severe bloating in the abdomen, greenish-tinged vomit, commonly causes severe inflammation or death of intestinal tissue purportedly as a result of using Simply Thick thickening agent.

The FDA in May 2010 issued a strict warning alleging that, although its investigation was ongoing, Simply Thick may be linked to the life threatening NEC condition, and therefore directed that “parents, caregivers and health care providers not feed Simply Thick to infants born before 37 weeks gestation who are currently receiving hospital care or have been discharged from the hospital in the past 30 days.”

In June 2011 the FDA reported 15 cases of life threatening NEC conditions suffered by premature infants after being fed Simply Thick, including two deaths.

Subject to additional FDA investigation, the recall only includes Simply Thick thickening gel products manufactured after June 1, 2009 by Thermo Pac, LLC at its Stone Mountain Georgia plant and not at two other manufacturing plants.

The Simply Thick thickening gel product is sold in individual packets/pouches, or in 64 ounce dispenser bottles and only the product manufactured at the Stone Mountain, Georgia plant is part of the current recall. TO DETERMINE IF YOUR SIMPLY THICK GEL WAS PART OF THE RECALL, please see below:

Products affected are 15 g, 30 g, 120 g and 240 g pouches:

All 15 g pouches are affected;
All 30 g pouches are affected;
Some 120 g pouches – identified as those with a “TP” in the lot code stamped into the edge of the packet;
Some 240 g pouches – identified as those with a “TP” in the lot code stamped into the edge of the packet.

Simply Thick item numbers affected:

ALL 01001, 01005, 01007, 02001, 02005, and 02007;
SOME 01004, 02004, 01006 and 02006 – identified as those with a “TP” in the lot code stamped into the edge of the packet;

Simply Thick item numbers are included as part of the UPC barcode on our packaging. The item number is the second group of 5 digits in the UPC barcode.

All products have a code embossed or stamped in the foil. The first 6 digits of that code represent a “best if used by” date in MMDDYY format. ANY date code that falls between 062610 (i.e. June 26, 2010) and 062612 (i.e. June 26, 2012) and contains the letter code “TP” in the code are affected by the recall.

An example of an affected date code is: 0312125TP1. The code breakdown would be the “Best If Used By Date”, 03/12/12 – i.e. March 12, 2012 AND it contains “TP” in the code .

Packets Code Dates Affected:

15 g packets (Nectar Individual Packets):

Embossed / Imprinted Date
080110#TP#
080210#TP#
082110#TP#
082210#TP#
082310#TP#
082410#TP#
082810#TP#
082910#TP#
092610#TP#
092710#TP#
092810#TP#
100310#TP#
101710#TP#
101810#TP#
101910#TP#
111310#TP#
111410#TP#
111510#TP#
111610#TP#
120410#TP#
121110#TP#
121210#TP#
010111#TP#
010211#TP#
010511#TP#
012911#TP#
013011#TP#
031311#TP#
031411#TP#
031511#TP#
032611#TP#
032711#TP#
032811#TP#
032911#TP#
041711#TP#
041811#TP#
050211#TP#
050311#TP#
050411#TP#
052111#TP#
052211#TP#
052311#TP#
052411#TP#
052511#TP#
052811#TP#
062611#TP#
062711#TP#
062811#TP#
062911#TP#
073111#TP#
080111#TP#
080211#TP#
080311#TP#
080411#TP#
080611#TP#
082711#TP#
082811#TP#
082911#TP#
091711#TP#
091811#TP#
091911#TP#
102911#TP#
103011#TP#
103111#TP#
110111#TP#
110211#TP#
110311#TP#
111211#TP#
111311#TP#
111411#TP#
111511#TP#
112011#TP#
112611#TP#
112711#TP#
120411#TP#
120511#TP#
120611#TP#
121011#TP#
121111#TP#
121211#TP#
121311#TP#
123111#TP#
010112#TP#
012212#TP#
012312#TP#
012412#TP#
012812#TP#
012912#TP#
013012#TP#
013112#TP#
020912#TP#
021212#TP#
021312#TP#
021412#TP#
021812#TP#
021912#TP#
031012#TP#
031112#TP#
031212#TP#
031312#TP#
031412#TP#
031912#TP#
032012#TP#
041412#TP#
041512#TP#
041612#TP#
050512#TP#
050612#TP#
050712#TP#
050812#TP#
050912#TP#
052112#TP#
052212#TP#
060212#TP#
060312#TP#
060412#TP#
060512#TP#

30 g Packets (Honey Individual Packets):

Embossed / Imprinted Date
062610#TP#
062710#TP#
080210#TP#
080310#TP#
082910#TP#
090410#TP#
090510#TP#
100310#TP#
100410#TP#
100510#TP#
101610#TP#
101710#TP#
120410#TP#
120510#TP#
120610#TP#
121210#TP#
121310#TP#
010211#TP#
010311#TP#
010411#TP#
030711#TP#
030811#TP#
030911#TP#
031211#TP#
031311#TP#
041611#TP#
041711#TP#
041911#TP#
042011#TP#
043011#TP#
050111#TP#
052811#TP#
052911#TP#
053011#TP#
060411#TP#
061811#TP#
061911#TP#
062011#TP#
080611#TP#
080711#TP#
080811#TP#
082911#TP#
083011#TP#
083111#TP#
091011#TP#
091111#TP#
091211#TP#
091711#TP#
100811#TP#
100911#TP#
101011#TP#
110511#TP#
110611#TP#
110711#TP#
110811#TP#
111911#TP#
112011#TP#
121011#TP#
121111#TP#
121211#TP#
121311#TP#
123111#TP#
010112#TP#
012212#TP#
012312#TP#
012812#TP#
012912#TP#
013012#TP#
013112#TP#
022012#TP#
022112#TP#
031712#TP#
031812#TP#
031912#TP#
041512#TP#
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041712#TP#
050512#TP#
050612#TP#
050712#TP#
050812#TP#
052212#TP#
052612#TP#
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052812#TP#

120g Packets (Nectar Bulk Packets)

Embossed / Imprinted Date
062710#TP#
080410#TP#
103110#TP#
110110#TP#
121910#TP#
122010#TP#
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102211#TP#
102311#TP#
120411#TP#
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032412#TP#
060912#TP#
061012#TP#

240g Packets (Honey Bulk Packets)

Embossed / Imprinted Date
062710#TP#
062810#TP#
080410#TP#
110110#TP#
110210#TP#
112010#TP#
112110#TP#
121810#TP#
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070211#TP#
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061112#TP#

Products manufactured at the Stone Mountain, GA plant subject to the voluntary recall were distributed across the United States and Canada through various food service and drug distributors, retail outlets, pharmacies, medical equipment suppliers, medical facilities, and directly to consumers. The voluntary recall is limited to only those products manufactured at the Stone Mountain, Georgia plant owned by Thermo Pac, LLC. Simply Thick products manufactured at two additional food processing plants are not affected.

If you or your child have suffered a serious injury by taking Simply Thick, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Zocor®

dom — Thu, 15 Sep 2011 01:09:12 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ZOCOR, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

You may need an attorney specializing in Zocor if you have suffered any of the serious side effects of the drug described further below. If you have been a victim of this drug and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Zocor falls into the statin pharmaceutical class and is a hypolipidemic drug that is frequently used in cholesterol control and hypercholesterolemia.

Also known as Simvastatin in generic form, this drug has also been used to increase HDLs and lower triglyceride levels. It is possible that Zocor might actually inhibit atherosclerosis progression, but this is still being studied. Current theories suggest that this may be due to the effect that Zocor has on macrophages present in lesions of atherosclerotic plaque. It has further been suggested that patients with more than one cardiovascular disease risk factor may possibly benefit from statins like Zocor even if their cholesterol levels are not yet elevated.

Common Adverse Effects of Zocor

Like all pharmaceuticals, Zocor can have adverse effects. The most common of which are:

· Diarrhea
· Weakness
· Indigestion
· Abdominal Pain
· Hives
· Itching
· Fatigue
· Fever
· Rashes

More Serious Adverse Effects of Zocor

Zocor also has some more serious side effects associated with its use. These adverse reactions include:

Zocor Dosage and Interactions

Zocor is available in dosages of 5 mg to as high as 80 mg. Zocor also has the ability to negatively interact with certain foods and other commonly prescribed medications. These include:

· Graprefruit – Individuals taking Zocor should refrain from eating grapefruit and other grapefruit products or drinking grapefruit juice because this will slow the matabolization of Zocor and cause toxicity risks.

· Amiodarone – Patients taking more than 20 mg of Zocor per day should refrain from using the drug in combination with Amiodarone, as this combination has a high risk of causing rhabdomyolysis. This condition can cause kidney failure and even death.

· Patients currently taking Clarithromycin, Erythromycin, Itraconazole, Ketoconazole, Nefazodone, Telithromycin and HIV protease inhibitors should not take Zocor in combination with these medications.

· Patients currently on a dosage of 10 mg of Zocor should not combine it with Cyclosporine, Danazol or Gemfibrozil.

· Patients taking 20 mg of Zocor should refrain from combining it with Verapamil.

· Patients taking 40 mg of Zocor should refrain from combining it with Diltiazem.

Merck is the maker of Zocor; however, the patent expired in June of 2006. Merck made a smart move at that time, choosing to reduce the price in order to remain competitive with companies offering generic forms of the drug. The result was that Merck was able to remain a key player in the game. In fact, two of the main health insurance companies in the United States, WellPoint and UnitedHealthcare, actually provide Zocor to members for the price of a generic copay drug.

If you have suffered a serious injury by taking Zocor, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Ethinyl Estradiol

dom — Thu, 15 Sep 2011 00:30:12 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ETHINYL ESTRADIOL, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Ethynyl estradiol is an orally bio-active estrogen used in almost all modern formulations of combined oral contraceptive pills like Yaz, Yasmin, Yasminelle, Ocella, Zarah, Syeda, Gianvi, Zafyral, Loryna, etc. There have been concerns raised regarding ethynyl estradiol’s safety and is thus not recommended as a first line agent. It is one of the most commonly used medications.

You may need an attorney specializing in ethynyl estradiol if you have suffered any of the serious side effects of the drug described further below. If you have been a victim of this drug and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Ethynyl estradiol is part of certain birth control formulations. The compound differs from other synthetic progestins in that its pharmacological profile in preclinical studies shows it to be closer to the natural progesterone. As such it has anti-mineralocorticoid properties, counteracts the estrogen-stimulated activity of the renin-angiotensin-aldosterone system, and is not androgenic. With its activities similar to spironolactone it may lead to less water retention and breast tenderness while improving skin appearance (less acne).

Adverse Reactions to Ethynyl Estradiol:

Ethynyl estradiol does have the potential for adverse reactions. Many of them are quite serious. These side effects can include the following:

· Decreased sex drive
· Spotting or bleeding between periods
· Headaches
· Nausea
· Vomiting
· Increased appetite
· Weight gain
· Vaginal discharge
· Yeast infections

More Serious Side Effects of Ethynyl Estradiol:

· Venous thromboembolism
· Breast lumps
· Heart attack
· Depression
· Other psychiatric issues
· Hyperkalemia
· Liver damage
· Hypertension
· Migraines
· Stroke
· Frequent vaginal bleeding
· Serious allergic reactions
· Pulmonary embolism
· Arrhythmia

Arrhythmias have been developed by women taking ethynyl estradiol. These are characterized by chest pain, fatigue, sweating, feeling anxious, and dizziness, fluttering in the chest or neck, palpitations, lightheadedness, shortness of breath and loss of consciousness. Severity of the arrhythmia will ultimately determine the type of treatment necessary, as well as other factors including age and medical history. Some serious arrhythmias require pacemakers or other implant devices, medications and surgeries, while many can be treated by reducing caffeine, nicotine and alcohol and introducing stress reduction and relaxation techniques into the lifestyle. There is no known cure for an arrhythmia.

More recently, several class action lawsuits have been filed against Bayer, who was the manufacturer of Yaz, a drug that contains ethynyl estradiol. These lawsuits came after Bayer failed to warn users appropriately of the dangerous side effects of its original drug, “Yaz”. These side effects can be fatal and the FDA did bring the hammer down on Bayer, demanding that the Yaz marketing campaigns be changed to A.) stop exaggerating the contraceptive’s abilities and B.) include proper notification of the public to the dangerous adverse effects of this contraceptive medication.

Any woman who develops any of the severe symptoms mentioned above should discontinue ethynyl estradiol and seek medical attention immediately to ensure that their health and well being are secure.

If you have suffered a serious injury by taking ethynyl estradiol, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Drospirenone

dom — Thu, 15 Sep 2011 00:00:04 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY DROSPIRENONE, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Drospirenone is a synthetic progestin that is used in popular birth control pills like: Yaz, Yasmin, Yasminelle, Ocella, Zarah, Syeda, Gianvi, Zafyral, Loryna, etc. There have been concerns raised regarding its safety and is thus not recommended as a first line agent.

You may need an attorney specializing in Drospirenone if you have suffered any of the serious side effects of the drug described further below. If you have been a victim of this drug and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Drospirenone is part of certain birth control formulations. The compound differs from other synthetic progestins in that its pharmacological profile in preclinical studies shows it to be closer to the natural progesterone. As such it has anti-mineralocorticoid properties, counteracts the estrogen-stimulated activity of the renin-angiotensin-aldosterone system, and is not androgenic. With its activities similar to spironolactone it may lead to less water retention and breast tenderness while improving skin appearance (less acne).

Adverse Reactions to Drospirenone:

Drospirenone does have the potential for adverse reactions. Many of them are quite serious. These side effects can include the following:

· Decreased sex drive
· Spotting or bleeding between periods
· Headaches
· Nausea
· Vomiting
· Increased appetite
· Weight gain
· Vaginal discharge
· Yeast infections

More Serious Side Effects of Drospirenone:

Arrhythmias have been developed by women taking Drospirenone. These are characterized by chest pain, fatigue, sweating, feeling anxious, and dizziness, fluttering in the chest or neck, palpitations, lightheadedness, shortness of breath and loss of consciousness. Severity of the arrhythmia will ultimately determine the type of treatment necessary, as well as other factors including age and medical history. Some serious arrhythmias require pacemakers or other implant devices, medications and surgeries, while many can be treated by reducing caffeine, nicotine and alcohol and introducing stress reduction and relaxation techniques into the lifestyle. There is no known cure for an arrhythmia.

More recently, several class action lawsuits have been filed against Bayer, who was the manufacturer of Yaz, a drug containing Drospirenone. These lawsuits came after Bayer failed to warn users appropriately of the dangerous side effects of its original drug, “Yaz”. These side effects can be fatal and the FDA did bring the hammer down on Bayer, demanding that the Yaz marketing campaigns be changed to A.) stop exaggerating the contraceptive’s abilities and B.) include proper notification of the public to the dangerous adverse effects of this contraceptive medication.

Any woman who develops any of the severe symptoms mentioned above should discontinue Drospirenone and seek medical attention immediately to ensure that their health and well being are secure.

If you have suffered a serious injury by taking Drospirenone, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Loryna®

dom — Wed, 14 Sep 2011 23:04:47 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY LORYNA, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

You may need an attorney specializing in the drug Loryna if you have suffered any of the serious side effects of the drug described further below. Loryna is a birth control pill manufactured by pharma giant Sandoz, Inc. Loryna is a generic version of Yaz, the controversial birth control pill marketed by Bayer (see below).

If you have been a victim of this drug and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Loryna is a type of birth control formula that contains drospirenone, which is essentially a synthetic progestin present in the birth control. Loryna is different from the various other forms of synthetic progestins as it is actually closer in makeup to natural progesterone. Because of this close pharmacological makeup, it may give users less breast tenderness and water retention while reducing the instance of acne. Loryna has also been used for the treatment of premenstrual dysphoric disorder and moderate acne.

Loryna is part of newer formulations of oral contraceptives. It contains 20 mcg of ethinylestradiol and 3 mg of drospirenone per tablet and it is used for contraceptive purposes. This contraceptive comes in a 24/4 style dosage, which means that the initial 24 pills will be active and contain the drospirenone and the last four pills will actually be placebo pills. Loryna works to change the uterine and cervical lining. This change prevents the sperm from reaching the uterus, as well as prevents fertilized eggs from attaching to the lining of the uterus. When Loryna is used according to the instructions, it is 99% effective in the prevention of pregnancy. However, that prevention does come at some risk.

Adverse Reactions to Loryna:

Loryna does have the potential for adverse reactions. Many of them are quite serious. These side effects can include the following:

· Decreased sex drive
· Spotting or bleeding between periods
· Headaches
· Nausea
· Vomiting
· Increased appetite
· Weight gain
· Vaginal discharge
· Yeast infections

More Serious Side Effects of Loryna:

Arrhythmias have been developed by women taking Loryna. These are characterized by chest pain, fatigue, sweating, feeling anxious, and dizziness, fluttering in the chest or neck, palpitations, lightheadedness, shortness of breath and loss of consciousness. Severity of the arrhythmia will ultimately determine the type of treatment necessary, as well as other factors including age and medical history. Some serious arrhythmias require pacemakers or other implant devices, medications and surgeries, while many can be treated by reducing caffeine, nicotine and alcohol and introducing stress reduction and relaxation techniques into the lifestyle. There is no known cure for an arrhythmia.

More recently, several class action lawsuits have been filed against Bayer, who is the manufacturer of Yaz. These lawsuits came after Bayer failed to warn users appropriately of the dangerous side effects of Yaz. These side effects can be fatal and the FDA did bring the hammer down on Bayer, demanding that the Yaz marketing campaigns be changed to A.) stop exaggerating the contraceptive’s abilities and B.) include proper notification of the public to the dangerous adverse effects of this contraceptive medication.

Any woman who develops any of the severe symptoms mentioned above should discontinue Loryna and seek medical attention immediately to ensure that their health and well being are secure.

If you have suffered a serious injury by taking Loryna, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Yaz 28®

dom — Wed, 14 Sep 2011 20:22:16 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY YAZ 28, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

You may need an attorney specializing in the drug Yaz 28 if you have suffered any of the serious side effects of the drug described further below. If you have been a victim of this drug and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Yaz 28 is a type of birth control formula that contains drospirenone, which is essentially a synthetic progestin present in the birth control. Yaz 28 is different from the various other forms of synthetic progestins as it is actually closer in makeup to natural progesterone. Because of this close pharmacological makeup, it may give users less breast tenderness and water retention while reducing the instance of acne. Yaz has also been used for the treatment of premenstrual dysphoric disorder and moderate acne.

Yaz 28 is part of newer formulations of oral contraceptives. It contains 20 mcg of ethinylestradiol and 3 mg of drospirenone per tablet and it is used for contraceptive purposes. This contraceptive comes in a 24/4 style dosage, which means that the initial 24 pills will be active and contain the drospirenone and the last four pills will actually be placebo pills. Yaz 28 works to change the uterine and cervical lining. This change prevents the sperm from reaching the uterus, as well as prevents fertilized eggs from attaching to the lining of the uterus. When Yaz 28 is used according to the instructions, it is 99% effective in the prevention of pregnancy. However, that prevention does come at some risk.

Adverse Reactions to Yaz 28:

Yaz 28 does have the potential for adverse reactions. Many of them are quite serious. These side effects can include the following:

· Decreased sex drive
· Spotting or bleeding between periods
· Headaches
· Nausea
· Vomiting
· Increased appetite
· Weight gain
· Vaginal discharge
· Yeast infections

More Serious Side Effects of Yaz 28:

Arrhythmias have been developed by women taking Yaz 28. These are characterized by chest pain, fatigue, sweating, feeling anxious, and dizziness, fluttering in the chest or neck, palpitations, lightheadedness, shortness of breath and loss of consciousness. Severity of the arrhythmia will ultimately determine the type of treatment necessary, as well as other factors including age and medical history. Some serious arrhythmias require pacemakers or other implant devices, medications and surgeries, while many can be treated by reducing caffeine, nicotine and alcohol and introducing stress reduction and relaxation techniques into the lifestyle. There is no known cure for an arrhythmia.

Any woman who develops any of the severe symptoms mentioned above should discontinue Yaz 28 and seek medical attention immediately to ensure that their health and well being are secure.

If you have suffered a serious injury by taking Yax 28, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Syeda®

dom — Wed, 14 Sep 2011 19:57:04 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY SYEDA, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

You may need an attorney specializing in the drug Syeda if you have suffered any of the serious side effects of the drug described further below. If you have been a victim of this drug and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Manufactured by Barr Pharmaceuticals, the drug Syeda is being marketed by Sandoz, the generics arm of Swiss drug maker Novartis, as a birth control pill that prevents ovulation and egg fertilization. The drug is a generic version of Bayer HealthCare Pharmaceuticals’ Yasmin.

Syeda is a type of birth control formula that contains drospirenone, which is essentially a synthetic progestin present in the birth control. Syeda is different from the various other forms of synthetic progestins as it is actually closer in makeup to natural progesterone. Because of this close pharmacological makeup, it may give users less breast tenderness and water retention while reducing the instance of acne. Syeda has also been used for the treatment of premenstrual dysphoric disorder and moderate acne.

Ocella is part of newer formulations of oral contraceptives. It contains ethinylestradiol and drospirenone and it is used for contraceptive purposes. This contraceptive comes in a 24/4 style dosage, which means that the initial 24 pills will be active and contain the drospirenone and the last four pills will actually be placebo pills. Syeda works to change the uterine and cervical lining. This change prevents the sperm from reaching the uterus, as well as prevents fertilized eggs from attaching to the lining of the uterus. When Syeda is used according to the instructions, it is 99% effective in the prevention of pregnancy. However, that prevention does come at some risk.

Adverse Reactions to Syeda

Syeda does have the potential for adverse reactions. Many of them are quite serious. These side effects can include the following:

· Decreased sex drive
· Spotting or bleeding between periods
· Headaches
· Nausea
· Vomiting
· Increased appetite
· Weight gain
· Vaginal discharge
· Yeast infections

More Serious Side Effects of Syeda:

Arrhythmias have been developed by women taking Syeda. These are characterized by chest pain, fatigue, sweating, feeling anxious, and dizziness, fluttering in the chest or neck, palpitations, lightheadedness, shortness of breath and loss of consciousness. Severity of the arrhythmia will ultimately determine the type of treatment necessary, as well as other factors including age and medical history. Some serious arrhythmias require pacemakers or other implant devices, medications and surgeries, while many can be treated by reducing caffeine, nicotine and alcohol and introducing stress reduction and relaxation techniques into the lifestyle. There is no known cure for an arrhythmia.

More recently, several class action lawsuits have been filed against Bayer, who was the manufacturer of Yaz. These lawsuits came after Bayer failed to warn users appropriately of the dangerous side effects of its original drug, “Yaz”. These side effects can be fatal and the FDA did bring the hammer down on Bayer, demanding that the Yaz marketing campaigns be changed to A.) stop exaggerating the contraceptive’s abilities and B.) include proper notification of the public to the dangerous adverse effects of this contraceptive medication.

Any woman who develops any of the severe symptoms mentioned above should discontinue Syeda and seek medical attention immediately to ensure that their health and well being are secure.

If you have suffered a serious injury by taking Syeda, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Zarah®

dom — Wed, 14 Sep 2011 19:20:05 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ZARAH, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

You may need an attorney specializing in the drug Zarah if you have suffered any of the serious side effects of the drug described further below. If you have been a victim of this drug and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Manufactured by Watson Laboratories, the drug Zarah is being marketed as a birth control pill that prevents ovulation and egg fertilization.

Zarah is a type of birth control formula that contains drospirenone, which is essentially a synthetic progestin present in the birth control. Zarah is different from the various other forms of synthetic progestins as it is actually closer in makeup to natural progesterone. Because of this close pharmacological makeup, it may give users less breast tenderness and water retention while reducing the instance of acne. Zarah has also been used for the treatment of premenstrual dysphoric disorder and moderate acne.

Zarah is part of newer formulations of oral contraceptives. It contains ethinylestradiol and drospirenone and it is used for contraceptive purposes. This contraceptive comes in a 24/4 style dosage, which means that the initial 24 pills will be active and contain the drospirenone and the last four pills will actually be placebo pills. Zarah works to change the uterine and cervical lining. This change prevents the sperm from reaching the uterus, as well as prevents fertilized eggs from attaching to the lining of the uterus. When Zarah is used according to the instructions, it is 99% effective in the prevention of pregnancy. However, that prevention does come at some risk.

Adverse Reactions to Zarah

Zarah does have the potential for adverse reactions. Many of them are quite serious. These side effects can include the following:

· Decreased sex drive
· Spotting or bleeding between periods
· Headaches
· Nausea
· Vomiting
· Increased appetite
· Weight gain
· Vaginal discharge
· Yeast infections

More Serious Side Effects of Zarah:

Arrhythmias have been developed by women taking Zarah. These are characterized by chest pain, fatigue, sweating, feeling anxious, and dizziness, fluttering in the chest or neck, palpitations, lightheadedness, shortness of breath and loss of consciousness. Severity of the arrhythmia will ultimately determine the type of treatment necessary, as well as other factors including age and medical history. Some serious arrhythmias require pacemakers or other implant devices, medications and surgeries, while many can be treated by reducing caffeine, nicotine and alcohol and introducing stress reduction and relaxation techniques into the lifestyle. There is no known cure for an arrhythmia.

Any woman who develops any of the severe symptoms mentioned above should discontinue Zarah and seek medical attention immediately to ensure that their health and well being are secure.

If you have suffered a serious injury by taking Zarah, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Safyral®

dom — Wed, 14 Sep 2011 19:02:50 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY SAFYRAL, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

You may need an attorney specializing in the drug Safyral if you have suffered any of the serious side effects of the drug described further below. If you have been a victim of this drug and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Manufactured by pharmaceutical giant Bayer, the drug Safyral is being marketed as a birth control pill that prevents ovulation and egg fertilization.

Safyral is a type of birth control formula that contains drospirenone, which is essentially a synthetic progestin present in the birth control. Safyral is different from the various other forms of synthetic progestins as it is actually closer in makeup to natural progesterone. Because of this close pharmacological makeup, it may give users less breast tenderness and water retention while reducing the instance of acne. Safyral has also been used for the treatment of premenstrual dysphoric disorder and moderate acne.

Safyral is part of newer formulations of oral contraceptives. It contains ethinylestradiol and drospirenone and it is used for contraceptive purposes. This contraceptive comes in a 24/4 style dosage, which means that the initial 24 pills will be active and contain the drospirenone and the last four pills will actually be placebo pills. Safyral works to change the uterine and cervical lining. This change prevents the sperm from reaching the uterus, as well as prevents fertilized eggs from attaching to the lining of the uterus. When Safyral is used according to the instructions, it is 99% effective in the prevention of pregnancy. However, that prevention does come at some risk.

Adverse Reactions to Safyral

Safyral does have the potential for adverse reactions. Many of them are quite serious. These side effects can include the following:

· Decreased sex drive
· Spotting or bleeding between periods
· Headaches
· Nausea
· Vomiting
· Increased appetite
· Weight gain
· Vaginal discharge
· Yeast infections

More Serious Side Effects of Safyral:

Arrhythmias have been developed by women taking Safyral. These are characterized by chest pain, fatigue, sweating, feeling anxious, and dizziness, fluttering in the chest or neck, palpitations, lightheadedness, shortness of breath and loss of consciousness. Severity of the arrhythmia will ultimately determine the type of treatment necessary, as well as other factors including age and medical history. Some serious arrhythmias require pacemakers or other implant devices, medications and surgeries, while many can be treated by reducing caffeine, nicotine and alcohol and introducing stress reduction and relaxation techniques into the lifestyle. There is no known cure for an arrhythmia.

Any woman who develops any of the severe symptoms mentioned above should discontinue Safyral and seek medical attention immediately to ensure that their health and well being are secure.

If you have suffered a serious injury by taking Safyral, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Yasminelle®

dom — Wed, 14 Sep 2011 18:47:18 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY YASMINELLE, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

You may need an attorney specializing in the drug Yasminelle if you have suffered any of the serious side effects of the drug described further below. If you have been a victim of this drug and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Yasminelle is a type of birth control formula that contains drospirenone, which is essentially a synthetic progestin present in the birth control. Yasminelle is different from the various other forms of synthetic progestins as it is actually closer in makeup to natural progesterone. Because of this close pharmacological makeup, it may give users less breast tenderness and water retention while reducing the instance of acne. Yasminelle has also been used for the treatment of premenstrual dysphoric disorder and moderate acne.

Yasminelle is part of newer formulations of oral contraceptives. Each tablet contains 0.020 mg ethinylestradiol (as betadex clathrate) and 3 mg drospirenone and it is used for contraceptive purposes. This contraceptive comes in a 24/4 style dosage, which means that the initial 24 pills will be active and contain the drospirenone and the last four pills will actually be placebo pills. Yasminelle works to change the uterine and cervical lining. This change prevents the sperm from reaching the uterus, as well as prevents fertilized eggs from attaching to the lining of the uterus. When Yasmin is used according to the instructions, it is 99% effective in the prevention of pregnancy. However, that prevention does come at some risk.

Adverse Reactions to Yasminelle:

Yasminelle does have the potential for adverse reactions. Many of them are quite serious. These side effects can include the following:

· Decreased sex drive
· Spotting or bleeding between periods
· Headaches
· Nausea
· Vomiting
· Increased appetite
· Weight gain
· Vaginal discharge
· Yeast infections

More Serious Side Effects of Yasminelle:

Arrhythmias have been developed by women taking Yasminelle. These are characterized by chest pain, fatigue, sweating, feeling anxious, and dizziness, fluttering in the chest or neck, palpitations, lightheadedness, shortness of breath and loss of consciousness. Severity of the arrhythmia will ultimately determine the type of treatment necessary, as well as other factors including age and medical history. Some serious arrhythmias require pacemakers or other implant devices, medications and surgeries, while many can be treated by reducing caffeine, nicotine and alcohol and introducing stress reduction and relaxation techniques into the lifestyle. There is no known cure for an arrhythmia.

Any woman who develops any of the severe symptoms mentioned above should discontinue Yasminelle and seek medical attention immediately to ensure that their health and well being are secure.

If you have suffered a serious injury by taking Yasminelle, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Yasmin®

dom — Wed, 14 Sep 2011 17:48:41 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY YASMIN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

You may need an attorney specializing in the drug Yasmin if you have suffered any of the serious side effects of the drug described further below. If you have been a victim of this drug and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Yasmin is a type of birth control formula that contains drospirenone, which is essentially a synthetic progestin present in the birth control. Yasmin is different from the various other forms of synthetic progestins as it is actually closer in makeup to natural progesterone. Because of this close pharmacological makeup, it may give users less breast tenderness and water retention while reducing the instance of acne. Yasmin has also been used for the treatment of premenstrual dysphoric disorder and moderate acne.

Yasmin is part of newer formulations of oral contraceptives. It contains 30 mcg of ethinylestradiol and 3 mg of drospirenone per tablet and it is used for contraceptive purposes. This contraceptive comes in a 24/4 style dosage, which means that the initial 24 pills will be active and contain the drospirenone and the last four pills will actually be placebo pills. Yasmin works to change the uterine and cervical lining. This change prevents the sperm from reaching the uterus, as well as prevents fertilized eggs from attaching to the lining of the uterus. When Yasmin is used according to the instructions, it is 99% effective in the prevention of pregnancy. However, that prevention does come at some risk.

Adverse Reactions to Yasmin:

Yasmin does have the potential for adverse reactions. Many of them are quite serious. These side effects can include the following:

· Decreased sex drive
· Spotting or bleeding between periods
· Headaches
· Nausea
· Vomiting
· Increased appetite
· Weight gain
· Vaginal discharge
· Yeast infections

More Serious Side Effects of Yasmin:

Arrhythmias have been developed by women taking Yasmin. These are characterized by chest pain, fatigue, sweating, feeling anxious, and dizziness, fluttering in the chest or neck, palpitations, lightheadedness, shortness of breath and loss of consciousness. Severity of the arrhythmia will ultimately determine the type of treatment necessary, as well as other factors including age and medical history. Some serious arrhythmias require pacemakers or other implant devices, medications and surgeries, while many can be treated by reducing caffeine, nicotine and alcohol and introducing stress reduction and relaxation techniques into the lifestyle. There is no known cure for an arrhythmia.

Any woman who develops any of the severe symptoms mentioned above should discontinue Yasmin and seek medical attention immediately to ensure that their health and well being are secure.

If you have suffered a serious injury by taking Yasmin, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Gianvi®

dom — Wed, 14 Sep 2011 17:32:47 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY GIANVI, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

You may need an attorney specializing in the drug Gianvi if you have suffered any of the serious side effects of the drug described further below. If you have been a victim of this drug and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

In June of 2010, Teva Pharmaceuticals announced that it would beginning marketing a generic form of the Yaz birth control pill under the trade name Gianvi. Without delay, Bayer (the manufacturer of Yaz) filed a patent infringement lawsuit against Teva arguing that Teva was in violation of a reciprocal agreement between the two companies.

Gianvi contains the exact same dose of ethinyl estradiol and drosperinone as Yaz. It is a type of birth control formula that contains drospirenone, which is essentially a synthetic progestin present in the birth control. Gianvi is different from the various other forms of synthetic progestins as it is actually closer in makeup to natural progesterone. Because of this close pharmacological makeup, it may give users less breast tenderness and water retention while reducing the instance of acne. Gianvi has also been used for the treatment of premenstrual dysphoric disorder and moderate acne.

Gianvi is part of newer formulations of oral contraceptives. It contains 20 mcg of ethinylestradiol and 3 mg of drospirenone per tablet and it is used for contraceptive purposes. This contraceptive comes in a 24/4 style dosage, which means that the initial 24 pills will be active and contain the drospirenone and the last four pills will actually be placebo pills. Gianvi works to change the uterine and cervical lining. This change prevents the sperm from reaching the uterus, as well as prevents fertilized eggs from attaching to the lining of the uterus. When Gianvi is used according to the instructions, it is 99% effective in the prevention of pregnancy. However, that prevention does come at some risk.

Adverse Reactions to Gianvi:

Gianvi does have the potential for adverse reactions. Many of them are quite serious. These side effects can include the following:

· Decreased sex drive

· Spotting or bleeding between periods

· Headaches

· Nausea

· Vomiting

· Increased appetite

· Weight gain

· Vaginal discharge

· Yeast infections

More Serious Side Effects of Gianvi:

· Venous thromboembolism

· Breast lumps

· Heart attack

· Depression

· Other psychiatric issues

· Hyperkalemia

· Liver damage

· Hypertension

· Migraines

· Stroke

· Frequent vaginal bleeding

· Serious allergic reactions

· Pulmonary embolism

· Arrhythmia

Arrhythmias have been developed by women taking Gianvi. These are characterized by chest pain, fatigue, sweating, feeling anxious, and dizziness, fluttering in the chest or neck, palpitations, lightheadedness, shortness of breath and loss of consciousness. Severity of the arrhythmia will ultimately determine the type of treatment necessary, as well as other factors including age and medical history. Some serious arrhythmias require pacemakers or other implant devices, medications and surgeries, while many can be treated by reducing caffeine, nicotine and alcohol and introducing stress reduction and relaxation techniques into the lifestyle. There is no known cure for an arrhythmia.

Any woman who develops any of the severe symptoms mentioned above should discontinue Beyaz and seek medical attention immediately to ensure that their health and well being are secure.

If you have suffered a serious injury by taking Gianvi, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Ocella®

dom — Wed, 14 Sep 2011 16:56:27 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY OCELLA, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

You may need an attorney specializing in the drug Ocella if you have suffered any of the serious side effects of the drug described further below. If you have been a victim of this drug and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Manufactured by Barr Pharmaceuticals, the drug Ocella originally hit the market in the year 2008. It is market as a birth control pill that prevents ovulation and egg fertilization.

Ocella is a type of birth control formula that contains drospirenone, which is essentially a synthetic progestin present in the birth control. Beyaz is different from the various other forms of synthetic progestins as it is actually closer in makeup to natural progesterone. Because of this close pharmacological makeup, it may give users less breast tenderness and water retention while reducing the instance of acne. Beyaz has also been used for the treatment of premenstrual dysphoric disorder and moderate acne.

Ocella is part of newer formulations of oral contraceptives. It contains ethinylestradiol and drospirenone and it is used for contraceptive purposes. This contraceptive comes in a 24/4 style dosage, which means that the initial 24 pills will be active and contain the drospirenone and the last four pills will actually be placebo pills. Ocella works to change the uterine and cervical lining. This change prevents the sperm from reaching the uterus, as well as prevents fertilized eggs from attaching to the lining of the uterus. When Ocella is used according to the instructions, it is 99% effective in the prevention of pregnancy. However, that prevention does come at some risk.

Adverse Reactions to Ocella

Ocella does have the potential for adverse reactions. Many of them are quite serious. These side effects can include the following:

· Decreased sex drive
· Spotting or bleeding between periods
· Headaches
· Nausea
· Vomiting
· Increased appetite
· Weight gain
· Vaginal discharge
· Yeast infections

More Serious Side Effects of Ocella:

Arrhythmias have been developed by women taking Ocella. These are characterized by chest pain, fatigue, sweating, feeling anxious, and dizziness, fluttering in the chest or neck, palpitations, lightheadedness, shortness of breath and loss of consciousness. Severity of the arrhythmia will ultimately determine the type of treatment necessary, as well as other factors including age and medical history. Some serious arrhythmias require pacemakers or other implant devices, medications and surgeries, while many can be treated by reducing caffeine, nicotine and alcohol and introducing stress reduction and relaxation techniques into the lifestyle. There is no known cure for an arrhythmia.

Any woman who develops any of the severe symptoms mentioned above should discontinue Ocella and seek medical attention immediately to ensure that their health and well being are secure.

If you have suffered a serious injury by taking Ocella, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Beyaz®

dom — Wed, 14 Sep 2011 16:05:02 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY BEYAZ, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

You may need an attorney specializing in the drug Beyaz if you have suffered any of the serious side effects of the drug described further below. If you have been a victim of this drug and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Beyaz is a type of birth control formula that contains drospirenone, which is essentially a synthetic progestin present in the birth control. Beyaz is different from the various other forms of synthetic progestins as it is actually closer in makeup to natural progesterone. Because of this close pharmacological makeup, it may give users less breast tenderness and water retention while reducing the instance of acne. Beyaz has also been used for the treatment of premenstrual dysphoric disorder and moderate acne.

Beyaz is part of newer formulations of oral contraceptives. It contains 20 mcg of ethinylestradiol and 3 mg of drospirenone per tablet and it is used for contraceptive purposes. This contraceptive comes in a 24/4 style dosage, which means that the initial 24 pills will be active and contain the drospirenone and the last four pills will actually be placebo pills. Beyaz works to change the uterine and cervical lining. This change prevents the sperm from reaching the uterus, as well as prevents fertilized eggs from attaching to the lining of the uterus. When Beyaz is used according to the instructions, it is 99% effective in the prevention of pregnancy. However, that prevention does come at some risk.

Adverse Reactions to Beyaz:

Beyaz does have the potential for adverse reactions. Many of them are quite serious. These side effects can include the following:

· Decreased sex drive
· Spotting or bleeding between periods
· Headaches
· Nausea
· Vomiting
· Increased appetite
· Weight gain
· Vaginal discharge
· Yeast infections

More Serious Side Effects of Beyaz:

Arrhythmias have been developed by women taking Beyaz. These are characterized by chest pain, fatigue, sweating, feeling anxious, and dizziness, fluttering in the chest or neck, palpitations, lightheadedness, shortness of breath and loss of consciousness. Severity of the arrhythmia will ultimately determine the type of treatment necessary, as well as other factors including age and medical history. Some serious arrhythmias require pacemakers or other implant devices, medications and surgeries, while many can be treated by reducing caffeine, nicotine and alcohol and introducing stress reduction and relaxation techniques into the lifestyle. There is no known cure for an arrhythmia.

Any woman who develops any of the severe symptoms mentioned above should discontinue Beyaz and seek medical attention immediately to ensure that their health and well being are secure.

If you have suffered a serious injury by taking Beyaz, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

Zelnorm

dom — Fri, 09 Sep 2011 21:19:58 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ZELNORM, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Zelnorm® is also known by its generic name, Tegaserod, and is considered a 5-HT4 agonist. Novartis manufactures the drug for use in the management of constipation and IBS (irritable bowel syndrome). The drug was originally FDA approved in 2002; however, in late March of 2007, it was pulled off the market as the FDA believed it may have been causing unfavorable cardiovascular effects.

Prior to its market removal, Zelnorm was the one and only drug that the FDA had approved to assist with the relief of the symptoms of irritable bowel syndrome and chronic constipation. The drug acted as a stimulant for motility to stimulate gastrointestinal system motility as well as peristaltic reflex. Many claimed that the drug also reduced the abdominal pain associated with these issues.

Zelnorm had several reported side effects that were reported after studies had been conducted. These side effects can range from the minor and more common to the more extreme and serious and include:
· Body – Abdominal pain, facial edema, flushing
· Cardiovascular effects – angina pectoris, arrhythmia, heart attack, hypertension, hypotension,
stroke, syncope
· Central Nervous System – Anxiety, vertigo
· Female Reproductive System – unusually heavy menstrual bleeding, ovarian cysts
· Gastrointestinal – severe diarrhea, ischemic colitis
· Neoplasms – can cause breast cancer
· Psychiatric – anxiety, depression, concentration issues, appetite increaser, sleep disorders
· Skin – severe itching and increased sweating
The symptoms listed above that occurred most often in patients taking Zelnorm were the gastrointestinal and cardiovascular symptoms. Obviously, this was a major issue that the FDA noted in their decision to pull the drug altogether.

The FDA was prompted to pull Zelnorm from the U.S. market after receiving results of an analysis that had been performed on the drug. This analysis clearly linked Zelnorm to serious cardiovascular issues
which included stroke and heart attack. Since the drug has been removed, the FDA encourages anyone still using the drug to get medical attention as soon as possible if they should begin experiencing
dizziness, chest pain, shortness of breath, numbness, drooping eyelids, altered senses or any other stroke or heart attack symptoms.

Zelnorm was first approved, despite Public Citizen’s petitions to stop the approval, for use in women who had been suffering with IBS in 2002, albeit for short-term use only. Two years later, the FDA approved an expansion of Zelnorm’s uses. This expansion involved the drug being approved for women under 65 to use the drug for the treatment of chronic idiopathic constipation.

As previously touched on, the FDA’s decision was based on nearly 30 studies that involved in excess of 18,000 patients. What these studies revealed was that Zelnorm increased the patient’s risk of stroke, heart attack and angina. The FDA strongly recommends that anyone still using Zelnorm seriously consider halting use of the drug. This is especially true in patients that have recently developed hypotension, syncope, diarrhea, and ischemic colitis.

The FDA further stated that it has concluded that Zelnorm and any benefits that patients may see from its use fails to outweigh the risks associated with the drug for the majority of patients that it was initially approved for.

Levaquin Side Effects

dom — Thu, 10 Mar 2011 16:38:51 +0000

: Levaquin

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY LEVAQUIN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Levaquin (levofloxacin)

WARNING: THE FDA HAS NOTIFIED MANUFACTURERS OF FLUOROQUINOLONE ANTIMICROBIAL DRUGS THAT A BOXED WARNING IN THE PRODUCT CONCERNING THE INCREASED RISK OF TENDINITIS AND TENDON RUPTURE IS NECESSARY. THIS INCLUDES THE DRUG LEVOFLOXACIN. THE AGENCY HAS ALSO DETERMINED THAT IT IS NECESSARY FOR MANUFACTURERS OF THE DRUGS TO PROVIDE A MEDICATION GUIDE TO PATIENTS ABOUT POSSIBLE SIDE EFFECTS.

Severe effects of Levaquin:

- Severe allergic reactions
- Difficulty breathing and/or tightness in the chest
- Bloody or tarry stools
- Arrhythmia
- Decreased or painful urination
- Sore throat, or unusual cough
- Hallucinations
- Inability to move or bear weight on a joint or tendon area
- Mood or mental changes
- Severe or persistent diarrhea, stomach pains or cramps
- Severe or persistent dizziness,
- Lightheadedness
- Symptoms of high or low blood sugar
- Symptoms of liver problems (dark urine, loss of appetite, pale stools, jaundice)

If any of these severe side effects manifest themselves, you should see your doctor or seek medical help immediately.

Common side effects when using Levaquin:

- Constipation
- Diarrhea
- Dizziness
- Gas
- Headache
- Lightheadedness
- Nausea
- Stomach pain
- Insomnia

In clinical studies of Levaquin, the side effects that occurred in a group of people taking Levaquin were documented and compared to side effects that occurred in a similar group of people taking a different antibiotic. This methodology made it possible to see what side effects from using Levaquin occurred, how often they appeared, and how they compare to the group taking a different medication.

In 1 to 2 percent of Levaquin users, the following side effects manifested themselves:

- Yeast infections
- Shortness of breath
- Vomiting
- Indigestion or heartburn
- Water retention
- Pain at the injection site
- Vaginal irritation or infection

Rare side effects (less than 1 percent of users) from use of Levaquin include anemia, loss of appetite, vertigo, nosebleeds, ringing of the ears (tinnitus) and sensitivity to the sun.

If you have experienced adverse side effects from taking LEVAQUIN, you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

Qualaquin Side Effects

dom — Thu, 10 Mar 2011 16:22:41 +0000

Qualaquin

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY QUALAQUIN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Qualaquin (quinine sulfate). For the treatment of uncomplicated malaria caused by the parasite Plasmodium falciparum.

ISSUE: Due to continued reports of serious side effects in patients using Qualaquin “off-label” for night time leg cramps, the FDA has approved a risk management plan to warn against the use of this drug for such unapproved uses. Qualaquin should not be used for night time leg cramps. Qualaquin use may result in serious and life-threatening hematological reactions, including serious bleeding due to thrombocytopenia, and hemolytic-uremic syndrome/ thrombotic thrombocytopenic purpura, which in some cases may result in permanent kidney damage. In some patients, adverse reactions result in hospitalization and death.

Severe side effects of Qualaquin:

- Severe vomiting

- Diarrhea

- Vision or hearing problems

- Breathing difficulty

- Urinating less than usual or not at all

- Chest pain

- Increased or irregular heartbeats

- Shallow or weak breathing

- Severe dizziness or lightheadedness

- Severe nosebleed

- Unusual purple, brown, or red spots on your skin

- Jaundice

Allergic reactions may include hives, trouble breathing and swelling of the face, lips, tongue and/or throat. Seek emergency medical attention right away if any of these severe side effects occur when using Qualaquin.

Common side effects when using Qualaquin:

- Dizziness

- Headache

- Nausea

- Sweating

- Hypoglycemia, or low blood sugar

Complications:

In fewer than 1 percent of Qualaquin users, symptoms such as restlessness, asthma attacks, swelling of the lungs, increased or decreased blood pressure, coma, heart attack, disorientation, visual disturbances, night blindness, irregular color vision, deafness, kidney failure, kidney infection or inflammation and/or cardiac arrest can occur.

If you have experienced adverse side effects from taking QUALAQUIN, you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

Simvastatin Side Effects

dom — Wed, 09 Mar 2011 16:18:31 +0000

: Simvastatin

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY SIMVASTATIN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Simvastatin is a hypolipidemic drug used to control elevated cholesterol. It is a is a synthetic derivative of a fermentation product of Aspergillus terreus. It is marketed generically as well as under the trade names Zocor, Simlup, Simcard and Simvacor.

WARNING: THE FDA HAS WARNED THAT SIMVASTATIN INCREASES THE RISK OF MUSCLE INJURY FROM SIMVASTATIN. ALTHOUGH MUSCLE INJURY IS A RECOGNIZED SIDE EFFECT IN ALL STATINS, SIMVASTATINS POSE A GREATER RISK OF DEVELOPING MUSCLE INJURY, INCLUDING RHABDOMYOLYSIS, A SERIOUS FORM OF MYOPATHY, WHICH CAN LEAD TO KIDNEY DAMAGE OR FAILURE RESULTING IN DEATH.

Severe side effects of Simvastatin:

- Severe allergic reactions
- Change in urine volume or darkening or urine
- Arrhythmia
- Joint or muscle pain
- Numbness or tingling in the hands or feet
- Persistent dizziness or lightheadedness
- Persistent nausea or stomach pain
- Jaundice

Seek medical attention immediately if any of these severe effects occur when using Simvastatin.

Common Side Effects of Simvastatin:

- Headache
- Abdominal pain
- A general feeling of weakness
- Constipation
- Diarrhea
- Indigestion
- Flatulence
- Nausea
- Upper respiratory infections
- Muscle pain

These common side effects have been observed in more that 1 percent of the 21,000 people evaluated in simvastatin clinical studies.

Simvastatin use side effects and hair loss are also commonly observed. Simvastatin causes up to 50% lowering of blood cholesterol but impacts hair growth in a negative way. Cholesterol indirectly relates to the major hormones contributing to hair growth and a large amount of hair loss is observed as a side effect of simvastatin. Other rare side effects can be memory loss, depression, joint pain, flatulence and upper respiratory infections.

If you have experienced adverse side effects from taking SIMVASTATIN, you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

Avelox Side Effects

dom — Tue, 08 Mar 2011 16:41:28 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY AVELOX, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Avelox (moxifloxacin).

Moxifloxacin is used to treat a variety of bacterial infections. This medication belongs to a class of drugs called quinolone antibiotics.

WARNING: THE SAFETY AND EFFECTIVENESS OF MOXIFLOXACIN IN PEDIATRIC PATIENTS, ADOLESCENTS (LESS THAN 18 YEARS OF AGE), PREGNANT WOMEN, AND LACTATING WOMEN HAVE NOT BEEN ESTABLISHED. CONSULT YOUR HEALTHCARE PROFESSIONAL IF YOU BELONG TO ANY OF THESE GROUPS. FLUOROGQUINOLONES, INCLUDING AVELOX, ARE ASSOCIATED WITH AN INCREASED RISK OF TENDINITIS AND TENDON RUPTURE IN ALL AGES. THE RISK INCREASES IN PATIENTS OVER 60, OR IN PATIENTS TAKING CORTICOSTEROIDS.

Serious side effects of Avelox:

- Severe allergic reactions
- Diarrhea, bloody or tarry stools
- Burning, numbness, tingling, pain, or weakness of the arms, hands, legs, or feet
- Chest pain
- Dark urine or decreased urination
- Fainting, fever, chills, or unusual cough
- Failure to bear weight in a joint or tendon
- Arrhythmia
- Mood or mental changes
- Muscle pain or weakness
- Persistent sore throat
- Shortness of breath
- Stomach pain or cramps
- Yellowing of the skin or eyes

Quinolones have also been linked to photosensitivity and events affecting the central nervous system. Seek medical attention immediately if any of these severe side effects occur upon taking Avelox.

Common side effects of Avelox:

- Nausea
- Diarrhea
- Dizziness
- Signs of liver damage such as jaundice, upper-right abdominal pain, light-colored stools, dark urine
- Itching

Rare Avelox Side Effects:

- Yeast infection
- Vomiting
- Dry mouth
- Gas
- Thrush (a yeast infection of the mouth)
- Constipation
- Insomnia
- Drowsiness

These rare side effects manifest themselves in less than one percent of Avelox users. Because of the very low percentage, these effects are sometimes not caused by Avelox but by other factors.

If you have experienced adverse side effects from taking AVELOX, you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

Actonel Side Effects

dom — Tue, 08 Mar 2011 16:31:44 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY ACTONEL, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Actonel (risedronate).

Used to treat or prevent osteoporosis and to treat Paget’s disease of the bone.

IN MARCH 2010, THE FDA ANNOUNCED THAT IS WAS PERFORMING A SAFETY REVIEW OF DRUGS LIKE ACTONEL SPECIFICALLY TO SEE IF THERE IS A RISK OF FRACTURES TO THE FEMUR JUST BELOW THE HIP JOINT. PATIENTS WHO HAVE TAKEN THE DRUG FOR SEVERAL YEARS MAY BE SUSCEPTIBLE TO SUCH FRACTURES.

Serious Side Effects Actonel:

- Throat pain, chest pain, or difficulty swallowing (a sign of esophageal ulcers)
- Severe or persistent heartburn
- Severe bone, muscle, or joint pain
- Jaw or tooth problems
- Anxiety
- Arrhythmia (irregular heart rhythm)
- Groin or thigh pain
- Signs of an allergic reaction, including unexplained rash, hives, itching, and unexplained swelling.

If any of these symptoms manifest themselves, you should seek immediate medical attention by visiting your doctor or consulting a healthcare professional.

Common Side Effects of Actonel:

- Abdominal Pain
- Back Pain
- Diarrhea
- Hypertension
- Joint Pain
- UTI
- Nausea
- Dizziness
- Neck pain
- Muscle pain
- Prostate enlargement (in men), also known as benign prostatic hyperplasia or BPH
- Leg cramps

Actonel has been thoroughly studied in clinical trials, in which a group of people taking the drug have side effects documented and compared to a control group who were not taking the drug. A few of these possible side effects included infections, hernia, tumors, chest pain, depression, pneumonia and cataracts.

If you have experienced adverse side effects from taking ACTONEL, you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

Vytorin Side Effects

dom — Mon, 07 Mar 2011 18:28:39 +0000

: Vytorin

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY VITORYN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Vytorin (ezetimibe and simvastatin)

A prescription tablet intended to lower bad cholesterol in the blood and raise good cholesterol.

Common Side Effects of Vytorin:

- Headache – in up to 5.8% of users;
- Diarrhea – in up to 5% of users;
- Upper respiratory infection, such as common colds (up to 5% of users);
- Myalgia or muscle pain (up to 3.6% of users);
- Flu (up to 2.3% of users);
- Pain, including back pain (up to 2.3% of users);
- Pain in an extremity, arm or leg (up to 2.3% of users).

The FDA has issued warnings as of December 2010 that Vytorin can cause erectile dysfunction and interstitial lung disease.

Other reported side effects of Vytorin include:

- General feeling of weakness (asthenia)
- Indigestion (dyspepsia)
- Unexplained rashes
- Abdominal pain (stomach pain)
- Eczema
- Bronchitis
- Urinary tract infection (UTI)
- Insomnia
- Constipation
- Gas
- A spinning sensation (vertigo)
- Sinus infection or inflammation
- Joint pain

Seek medical attention immediately if any of these SEVERE side effects manifest themselves when you use Vytorin: Severe allergic reactions (rash; hives; itching; difficulty breathing or swallowing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred vision or vision changes; change in urine volume; chest pain; dark urine; depression; fast heartbeat; fever; appetite loss; muscle tenderness, pain, or weakness (with or without fever and fatigue); numbness, tingling, burning, or weakness in the arms, hands, feet, or legs; pale stools; stomach tenderness; unexplained pain in the stomach or mid-upper back; unusual bruising or bleeding; unusual tiredness; vomiting; yellowing of the skin or eyes.

Vytorin has also been linked to liver and kidney problems as well as gastrointestinal disorders, memory loss, irritability and personality changes.

If you have experienced severe, adverse side effects from taking VYTORIN, you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

Ketek Side Effects

dom — Mon, 07 Mar 2011 18:08:43 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY KETEK, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Ketek (Telithromycin).

Used to treat mild to moderate respiratory infections.

THE FDA HAS ANNOUNCED BOXED WARNINGS FOR THE USAGE OF KETEK. THE WARNINGS STATE THAT KETEK IS CONTRAINDICATED IN PATIENTS WITH THE CONDITION MYASTHENIA GRAVIS, A DISEASE THAT CAUSES WEAKNESS OF THE MUSCLES. THE CHANGE IN LABELING ALSO REMOVES ACUTE BACTERIAL SINUSITIS AND ACUTE BACTERIAL EXACERBATIONS AS APPROVED INDICATIONS IN KETEK’S LABEL.

Side Effects of Ketek:

- Mild nausea and/or vomiting
- Vaginal itching or discharge;
- Headache or dizziness.

Telithromycin may cause sudden and serious liver damage. In some cases, death may result from liver failure. Cease using the medication and consult your doctor immediately if symptoms such as nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, or jaundice manifest themselves.

Serious side effects of Ketek:

- Watery or bloody diarrhea
- Irregular heartbeat
- Feeling of light-headedness or fainting
- Vision problems (difficulty focusing, drooping eyelid)
- Muscle pain or weakness
- Difficulty swallowing
- Loss of balance, coordination, or ability to climb stairs
- Difficulty in rising from a chair

An internal FDA memo has cited 12 cases of acute liver failure and up to four deaths, and more than 20 other cases of severe liver damage. In cases of allergic reactions to Ketek (such as hives, difficulty breathing, swelling of your face, lips, tongue, or throat), seek emergency medical help immediately.

Ketek also reacts negatively with medications that contain cisapride (Propulsid) or pimozide (Orap).

It has revealed that Aventis failed to disclose integrity problems in its studies when it submitted the drug’s clinical trial results to the FDA. This flawed approval process and recent evidence of adverse Ketek side effects has led to a Congressional investigation on the FDA process behind the popular drug. In fact, a doctor has been convicted of mail fraud for submitting false clinical information related to Phase III of Ketek’s comparative study.

If you have experienced adverse side effects from taking KETEK, you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

Fosamax Side Effects

dom — Sat, 05 Mar 2011 01:34:13 +0000

: Fosamax FDA

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY FOSAMAX, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Fosamax (Alendronic Acid).

NEWS FLASH: FOSAMAX LINKED TO CASES OF LOW-IMPACT BONE FRACTURES AND OSTEONECROSIS OF THE JAW. MERCK, MAKER OF FOSAMAX, IS CURRENTLY FACING HUNDREDS OF LAWSUITS DUE TO HARMFUL BONE-RELATED SIDE EFFECTS. See Wikipedia.

Fosamax is a bisphosphonate drug used to treat or prevent osteoporosis and other bone diseases in both men and women.

Fosamax Common Side Effects

Frequently encountered side effects when taking Fosamax:

• Bone, muscle or joint pain
• Nausea
• Vomiting
• Mild stomach pain
• Headache
• Dizziness
• Diarrhea
• Constipation
• Bloated feeling

FOSAMAX LINKED TO REPORTS OF FEMORAL FRACTURES AND OSTEONECROSIS OF THE JAW (ONJ). If you have experienced adverse side effects from taking FOSAMAX [Bone fractures, esophageal ulcers, and any other serious health issues] you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

Fosamax Serious Side Effects:

• Severe allergic reactions
• Difficulty breathing
• Swelling
• Chest pain
• Coughing or vomiting blood
• Mouth sores
• Black, tarry or bloody stool
• Severe heart burn
• Severe sore throat
• Esophageal ulcer
• Osteonecrosis of the jaw
• Leg fractures

According to ABC News there is increasing evidence that the long-term use of Fosamax could result in spontaneous femoral fractures that can be triggered by light, low-energy exercises or any other physical activity. Three female Fosamax users, all over the age of 40, broke both femurs from simply walking or jumping rope.

Precautions. Questions for Your Doctor.

Patients who cannot take Fosamax are patients with esophageal problems, low blood calcium levels, digestive problems, malabsorption syndrome, kidney disease, stomach ulcer, and vitamin D deficiency. It is also not recommended to pregnant or breastfeeding mothers.

IT IS STRONGLY ADVISED THAT YOU SPEAK WITH A MEDICAL PROFESSIONAL, INFORM THEM OF YOUR HISTORY AND ANY CONDITIONS AND ADDRESS YOUR CONCERNS BEFORE USING FOSAMAX.

Fentanyl Side Effects

dom — Fri, 04 Mar 2011 20:57:55 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY FENTANYL, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Fentanyl; Also marketed as Sublimaze, Actiq, Durogesic, Duragesic, Fentora, Onsolis, Instanyl, and Abstral.

NEWS FLASH: FDA ISSUES SECOND SAFETY WARNING ON FENTANYL PATCH. THE SECOND WARNING WAS ISSUED BY THE FDA ON DEC. 21, 2007 IN RESPONSE TO CONTINUED REPORTS OF DEATHS AND LIFE-ENDANGERING SIDE EFFECTS ASSOCIATED WITH THE FENTANYL SKIN PATCH. See FDA web site.

The Fentanyl transdermal system is a skin patch that is used to alleviate moderate to severe chronic pain. It is about 100 times stronger than morphine and works extremely fast.

Fentanyl Common Side Effects

Fentanyl patches, especially when not used properly, can often elicit adverse side effects such as:

• Diarrhea
• Constipation
• Dry mouth
• Somnolence
• Confusion
• Dizziness
• Weakness
• Sweating
• Difficulty in breathing

FENTANYL PATCHES CAN LEAD TO SERIOUS HARM OR EVEN DEATH. If you have experienced adverse side effects from using FENTANYL PATCHES [Severe allergic reactions, liver damage, and any other serious health issues] you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 1-888-736-4248.

• Fentanyl Serious Side Effects
• Addiction
• Respiratory depression
• Liver damage
• Severe allergic reaction
• Death

There have been many cases of fatal overdoses associated with fentanyl products throughout the past few years, causing the FDA to issue two consecutive safety warnings about the product. Manufacturers subsequently recalled Fentanyl products after it was revealed that some of the deaths reported were due to faulty patches that leaked too much of the product into the skin, causing respiratory depression, overdose, and death. However, according to the FDA, some deaths were also due to incorrect prescriptions and improper use of the patch.

Precautions. Questions for Your Doctor.

Fentanyl patches should not be prescribed to patients who have acute or sever bronchial asthma, paralytic ileus, and those who are not opioid-tolerant. It is also not to be used for sudden, sporadic, or mild pain, as well as post-surgery pain.

Correct usage of the patch is extremely crucial in avoiding life-threatening side effects or fatalities. Patients must take care to read and follow the instructions precisely. It is also important to avoid sources of heat while wearing the patch as high temperatures can cause increased skin permeation of the drug.

IT IS STRONGLY ADVISED THAT YOU SPEAK WITH A MEDICAL PROFESSIONAL, INFORM THEM OF YOUR HISTORY AND ANY CONDITIONS AND ADDRESS YOUR CONCERNS BEFORE USING FENTANYL PATCHES.

Chantix Side Effects

dom — Thu, 03 Mar 2011 15:42:33 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY CHANTIX, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Chantix (Varenicline). Also marketed as Champix.

NEWS FLASH: FDA ANNOUNCES “BLACK BOX” WARNINGS ON CHANTIX LABELS DUE TO REPORTS OF MENTAL HEALTH ISSUES IN USERS. FDA ANALYSIS REVEALS THAT THE USE OF CHANTIX CAN ELICIT ADVERSE PSYCHIATRIC SYMPTOMS, AS WELL AS WORSEN THE CONDITION OF THOSE WITH PRE-EXISTING MENTAL ILLNESSES. See FDA website.

Chantix is a nicotine-free prescription drug formulated primarily for smoking cessation purposes.

Chantix Common Side Effects:

• Nausea
• Headache
• Difficulty sleeping
• Strange dreams or nightmares
• Heartburn
• Vomiting
• Sleeping disorder
• Gas
• Constipation

FDA BLACK BOX WARNING ON CHANTIX. If you have experienced adverse side effects from taking CHANTIX [suicidal thoughts, seizures, or any other neuropsychiatric symptoms] you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

Chantix Serious Side Effects:

• Depression
• Hostility
• Suicidal tendencies
• Mood swings
• Psychosis
• Homicidal impulses
• Seizures
• Hallucinations
• Swelling of face, mouth, tongue, arms, legs or throat
• Other psychiatric issues

An analysis by the Institute for Safe Medication Practices (ISMP) revealed that over 1,000 cases of serious injuries, traffic accidents and falls, life-threatening heart rhythm disturbances, heart attacks, severe skin reactions, diabetes, seizures, psychosis, aggression, homicidal ideation, and suicide were reported to the FDA between 2006 to 2007, all of them attributed to the use of Varenicline, the trade name of Chantix. It also showed evidence connecting the smoking cessation drug to seriously harmful allergic reactions.

Precautions. Questions for Your Doctor.

Due to reports of amplified psychiatric problems in some Chantix users, patients with a history of mental illness are advised to avoid using the drug as it can further intensify their symptoms.

Other patients who should not be prescribed Chantix are pregnant or breastfeeding mothers, women who are trying to get pregnant, and people with a history of kidney problems.

IT IS STRONGLY ADVISED THAT YOU SPEAK WITH A MEDICAL PROFESSIONAL, INFORM THEM OF YOUR HISTORY AND ANY CONDITIONS AND ADDRESS YOUR CONCERNS BEFORE USING CHANTIX.

Wellbutrin Side Effects

dom — Thu, 03 Mar 2011 15:22:36 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY WELLBUTRIN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Wellbutrin (Bupropion). Also marketed as Zyban, Voxra, Budeprion, and Aplenzin.

NEWS FLASH: WELLBUTRIN REQUIRED TO CARRY “BLACK BOX” WARNING AFTER BEING LINKED TO INCREASE IN SUICIDAL BEHAVIOR. THE FDA WARNS THAT THE USE OF WELLBUTRIN COULD LEAD TO NEUROPSYCHIATRIC SYMPTOMS SUCH AS INTENSE RAGE AND SUICIDAL THOUGHTS See US Recall News website.

Wellbutrin is an antidepressant medication that is prescribed to those who suffer from clinical depression. It is also used as a smoking cessation aid.

Wellbutrin Common Side Effects:

It has been observed that users of Wellbutrin may experience the following symptoms:

• Agitation
• Weight loss
• Dry mouth
• Constipation
• Headache
• Nausea or vomiting
• Increased sweating
• Tremors
• Insomnia
• Appetite loss
• Blurred vision
• Increased heart rate or irregular heart rhythm
• Confusion
• Aggressiveness or hostility

FDA BLACK BOX WARNING ON WELLBUTRIN. If you have experienced adverse side effects from taking WELLBUTRIN [suicidal thoughts, seizures, or any other neuropsychiatric symptoms] you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 1-888-736-4248.

Wellbutrin Serious Side Effects:

• Seizures
• Suicidal ideation
• Hypertension
• Bouts of intense rage
• Mania
• Other psychotic symptoms

According to the eMedTV website, about 4 out of every 1,000 Wellbutrin users have experienced seizure episodes, which is one of the most controversial side effects of the drug. It is said that the risk of seizures is greater at the start of treatment.

Also, the FDA has issued a warning regarding the possible association of Wellbutrin with suicidal tendencies. “Black box” warnings are now required to appear on all Wellbutrin labels after occurrences of suicidal behavior have been observed in users with no history of mental disorders. Possible symptoms that patients may encounter include behavior changes, aggressiveness, agitation, depression, and suicidal tendencies.

Precautions. Questions for Your Doctor.

The use of Wellbutrin can be potentially dangerous to those who suffer from or have a history of epilepsy or seizure disorder, head injury, brain tumor, high blood pressure, heart disease, kidney and liver problems, and bipolar disorder.

IT IS STRONGLY ADVISED THAT YOU SPEAK WITH A MEDICAL PROFESSIONAL, INFORM THEM OF YOUR HISTORY AND ANY CONDITIONS AND ADDRESS YOUR CONCERNS BEFORE USING WELLBUTRIN.

Fixodent Side Effects

dom — Thu, 03 Mar 2011 04:43:37 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY FIXODENT, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Fixodent (Denture Cream).

NEWS FLASH: LAWSUIT FILED AGAINST MAKERS OF FIXODENT DUE TO ALLEGED REPORTS OF IRREPARABLE NERVE DAMAGE IN FREQUENT USERS. See ABC NEWS WEBSITE.

Fixodent is a denture adhesive that secures ill-fitting dentures to the mouth and allows wearers to be able chew faster and more naturally as they did with their own teeth.

Fixodent Adverse Side Effects

Fixodent, especially when used generously for a long period of time, has been alleged to cause the following:

• Zinc poisoning
• Copper depletion
• Peripheral neuropathy

Users who develop peripheral neuropathy may encounter symptoms such as:

• Numbness in limbs
• Inability to move limbs
• Tingling feelings
• Problems with balance
• Difficulty walking

FIXODENT MAY RESULT IN IRREPARABLE NERVE DAMAGE. If you have experienced adverse side effects from using Fixodent [zinc poisioning, nerve damage, and any other serious health issues] you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

As reported by ABC News, Proctor & Gamble faces a pending class-action lawsuit due to the alleged connection between the use of Fixodent and extreme nerve damage or peripheral neuropathy. Two long-time Fixodent users who have been diagnosed with zinc poisoning and irreparable nerve damage believe that their health issues are to be blamed on the zinc found in Fixodent.

Precautions. Questions for Your Doctor:

The ingestion of large amounts of zinc can lead to serious neurological problems. Fixodent users should take great caution when using the product as it may lead to irreversible adverse side effects.

IT IS STRONGLY ADVISED THAT YOU SPEAK WITH A MEDICAL PROFESSIONAL, INFORM THEM OF YOUR HISTORY AND ANY CONDITIONS, IN ADDITION TO ADDRESSING YOUR CONCERNS BEFORE TAKING FIXODENT.

Related Posts:
Polygrip Side Effects
Denture Cream Recall

Polygrip Side Effects

dom — Thu, 03 Mar 2011 04:33:13 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY POLYGRIP, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Polygrip (Denture Cream) also marketed as Super Poligrip Original, Super Poligrip Ultra Fresh and Super Poligrip Extra Care.

NEWS FLASH: POLYGRIP TO BE RECALLED DUE TO ITS ALLEGED CONNECTION TO NEUROLOGICAL ILLNESSES; GlaxoSmithKline to reformulate Polygrip denture creams after facing lawsuits due to reports of nerve damage in users. See NEWSMAX HEALTH WEBSITE.

Polygrip is a denture cream that acts as an adhesive to secure ill-fitting dentures to the mouth. It allows wearers to chew faster and more naturally as they did with their own teeth.

Polygrip Adverse Side Effects

The long-term use of Polygrip could lead to the following illnesses:

• Zinc poisoning
• Copper depletion
• Peripheral neuropathy

Users who develop peripheral neuropathy may encounter symptoms such as:

• Numbness
• Tingling feeling
• Pain
• Weak muscles
• Loss of balance
• Difficulty walking
• Loss of sensation
• Paralysis

POLYGRIP MAY RESULT IN IRREPARABLE NERVE DAMAGE. If you have experienced adverse side effects from using Polygrip [zinc poisioning, nerve damage, and any other serious health issues] you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

According to NewsMaxHealth.com, GlaxoSmithKline, maker of the Polygrip denture creams, has announced that they will recall and reformulate their product and come up with a new formula that is totally zinc free. This is due to the many lawsuits they are now facing, as Polygrip is alleged to have caused severe nerve damage and blood problems in its users after long-term usage.

Precautions. Questions for Your Doctor:

Taking large amounts of zinc for a long period of time can lead to peripheral neuropathy. Polygrip users should take great caution when using the product as it may lead to irreversible debilitating side effects.

IT IS STRONGLY ADVISED THAT YOU SPEAK WITH A MEDICAL PROFESSIONAL, INFORM THEM OF YOUR HISTORY AND ANY CONDITIONS IN ADDITION TO ADDRESSING YOUR CONCERNS BEFORE USING POLYGRIP.

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Meridia Side Effects

dom — Tue, 01 Mar 2011 03:26:34 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY MERIDIA, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Meridia (also known as Sibutramine) is a weight-reduction drug for people who have difficulty losing weight by means of the usual methods, such as dieting or exercising. It is prescribed for those who struggle with obesity and are medically at risk due to excessive body weight.

There are many frequent side effects that have been observed in patients using Meridia.

Meridia Common Side Effects

* dry mouth
* nausea
* dizziness
* migraines
* constipation
* insomnia
* confusion
* anxiety
* agitation
* fevers
* sweating
* vomiting
* upset stomach
* diarrhea
* tremors
* joint or muscle pain
* acne

Strangely enough, despite the fact that it is a drug used to lose weight, Meridia has actually caused an increase in appetite for some users.

Serious Side Effects of Meridia

* seizures
* unusual bleeding or bruising
* melena
* vomiting of blood
* urination problems
* jaundice
* hemiplegia
* and more (see below).

Hence it is not recommended to those patients with a history of seizures or epilepsy, bleeding disorders, kidney diseases, and liver dysfunction.

Also, one of the most serious side effects associated with Meridia is heightened heart rate and blood pressure. Due to a surprisingly high number of cardiovascular incidents that have occurred in relation to the drug, it has been observed that Meridia is especially dangerous to patients with heart-related problems as it can further aggravate their condition. It may increase the possibility of developing severe heart diseases such as coronary artery disease, congestive heart failure, myocardial infarction, cardiac arrhythmia, and more.

Aside from the physical symptoms there have also been cases of psychological side effects. Meridia has been known to elicit extreme mood changes or serious mental problems. Therefore, it is strongly inadvisable to be used by those suffering from psychiatric illnesses, particularly those with bipolar disorder. Some patients have had bouts of restlessness, over-excitement, depression, psychosis, and even suicidal thoughts.

If you have experienced adverse side effects from taking MERIDIA [seizures, bleeding, bruising, melena, jaundice, hemiplegia, or any other serious health issues] you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

Multaq Side Effects

dom — Mon, 28 Feb 2011 20:29:21 +0000

Multaq (Dronedarone); Also known as SR33589.

NEWS FLASH: MULTAQ ASSOCIATED WITH SEVERE LIVER DAMAGE. IN JANUARY OF 2011, THE FDA ISSUED A WARNING REGARDING THE USE OF MULTAQ DUE TO REPORTS OF ACUTE LIVER FAILURE ASSOCIATED WITH THE DRUG See FDA WEBSITE (http://www.fda.gov/Drugs/DrugSafety/ucm240011.htm).

Multaq is used to treat irregular heartbeats in patients who have had atrial fibrillation (AFib) or atrial flutter (AFlutter) throughout the past 6 months. The use of this drug can also help reduce the risk of being hospitalized for cardiovascular problems.

Multaq Common Side Effects

Frequent symptoms that are encountered while using Multaq:

• Diarrhea
• Stomach pain
• Skin rashes
• Nausea
• Slowed heartbeats

MULTAQ COULD CAUSE LIVER FAILURE. If you have experienced adverse side effects from taking MULTAQ [Severe liver injury or failure, jaundice, and any other serious health issues] you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

Other Multaq Side Effects:

• Wheezing or shortness of breath
• Tightening chest
• Foamy mucus
• Sleeping problems due to difficulty in breathing
• Weight gain
• Leg swelling
• Fainting
• Itching
• Jaundice

The most prominent and dangerous side effect that has been associated with Multaq is severe liver injury. Two patients who were using Multaq have reportedly experienced acute liver failure, which required them to get liver transplants. These cases both occurred in elderly women at around 70 years of age. The first patient suffered liver failure after six months of using the drug while the other after about four and a half months.

Precautions. Questions for Your Doctor.

Accoding to the Multaq website, patients who have severe liver or heart problems should not use the drug as it may further aggravate their condition. There is also an increased chance of death for those who have suffered or are currently suffering from severe heart failure.

It is also not advisable for breastfeeding or expectant mothers as it is not yet certain whether or not it may harm their babies.

IT IS STRONGLY ADVISED THAT YOU SPEAK WITH A MEDICAL PROFESSIONAL, INFORM THEM OF YOUR HISTORY AND ANY CONDITIONS AND ADDRESS YOUR CONCERNS BEFORE USING MULTAQ.

Reglan Tardive Dyskinesia

dom — Sat, 26 Feb 2011 18:42:33 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY REGLAN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Reglan is used primarily to provide short-term relief to patients suffering from heartburn and esophagitis due to gastroesophageal reflux disease (GERD), though the FDA has warned against its use for more than 4 to 12 weeks at a time and advises restrictive prescription to patients who do not respond to alternative forms of therapy. Reglan is most helpful to those who experience heartburn during the daytime rather than at night. It is generally prescribed for use before meals that tend to cause heartburn in patients who only experience heartburn symptoms after eating certain foods.

Reglan may also be prescribed to relieve symptoms of heartburn and other uncomfortable conditions experienced by diabetics who are suffering from diabetic
gastric stasis.

If you or your family member has experienced Tardive Dyskinesia disorder or other serious injury from taking Reglan (Octamide/Maxolon) you may be entitled to compensation for your medical bills and for your pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

Related Posts:
Reglan Lawsuit
Reglan Side Effects

Reglan Side Effects

dom — Sat, 26 Feb 2011 18:35:46 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY REGLAN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

FDA Black Box Warning Issued on Reglan: In February 2009, Reglan and other metoclopramide containing drugs (Reglan/Octamide/Maxolon) were “black-boxed” by the F.D.A (strongest warning meant to call attention to possibly deadly or very serious side effect risks) warning consumers of the elevated risk of a condition known as tardive dyskinesia for people who take the drug in high doses and over a prolonged period. Tardive dyskinesia is a mostly irreversible, permanent tongue, mouth and jaw disorder which causes repetitive movements, such as rapid eye blinking, lip smacking, and face and body jerking, and tongue protrusion. It is a condition that tends to appear slowly, and for which there is, at present, no known cure. Under the FDA issuance, manufacturers were required to implement a risk evaluation and mitigation strategy, or REMS, to ensure patients are provided with a medication guide that discusses this risk.

“The FDA wants patients and health care professionals to know about this risk so they can make informed decisions about treatment,” said Doctor Janet Woodcock, director of the FDA’s Center for Drug Evaluation and Research. “The chronic use of metoclopramide therapy should be avoided in all but rare cases where the benefit is believed to outweigh the risk.”

Dr. Joseph Jankovic, a neurologist at Baylor College of Medicine in Houston, states about this condition” In some patients, the symptoms get better (once they are taken off the drug), “but in many cases, it becomes a permanent neurological disorder.”

Reglan (Octamide/Maxolon) Serious Side Effects Include:

• Tardive dyskinesia (neurological disorder causing involuntary movements, especially facial tic);
• Agranulocytosis (failure of the bone marrow to make sufficient white blood cells);
• Slow heart beat;
• Seizures;
• Aldosteronism (syndrome of high blood pressure and low blood potassium levels);
• Neuroleptic malignant syndrome (NMS);
• Endocrine disturbances;
• Liver problems;
• Disorders similar to Parkinson’s disease

If you have experienced adverse side effects from taking REGLAN, [Tardive Dyskinesia or other serious injury] you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. There are already numerous lawsuits throughout the U.S. for those alleging injury caused by Reglan, claiming among other things, that the drug’s manufacturer overstated the benefits and failed to adequately warn about the risk of severe injury linked to the drug. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

Related Posts:
Reglan Lawsuit
Reglan Tardive Dyskenesia

Reglan Lawsuit

dom — Sat, 26 Feb 2011 17:36:44 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY REGLAN, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Generic Name: Metoclopramide hydrochloride

Brand Names: Reglan, Octamide, Maxolon

Reglan Description:

Reglan is extremely popular drug for the treatment of heartburn and esophagitis due to gas reflux condition. It is also used to assist diabetics with diabetic gastroparesis, to treat nausea associated with surgery or cancer treatment, and to treat small intestine conditions. Reglan is intended for short term. Its use speeds up the muscle contractions that take place in the upper digestive tract of the stomach thereby helping solid and liquid food pass more quickly from the stomach into the intestines. For patients with gas reflux disease, it decreases the reflux of stomach acid, a condition that results in severe heart burn and damage to the esophagus due to the lower esophageal sphincter allowing stomach acid to rise up from the stomach.

Related Posts:
Reglan Side Effects
Reglan Tardive Dyskenesia

Yaz Side Effects

dom — Fri, 25 Feb 2011 21:42:57 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY YAZ, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

FDA Black Box Warning Issued on Yaz: Yaz has been “black-boxed” by the F.D.A (strongest warning meant to call attention to possibly deadly or very serious side effect risks) warning consumers of the elevated risk of cardiovascular side effects, such as blood clots, strokes and heart attacks in patients who smoke while taking the medicine. The warning states that this risk increases with age and for woman over 35 who smoke 15 or more cigarettes daily.

2009 Recall: In November 2009, Bayer was cited once again for sending low-quality batches of drosperinone to doctors and pharmacies. Under FDA pressure, Bayer recalled 33,000 boxes of Yaz and 122,208 boxes of Ocella. Each box contains three packages of one month’s supply of the birth control pills. The lot numbers for the recalled Ocella tablets are 84080A and 84081A. The lot number for the recalled Yaz tablets is 91605A. Bayer justified the defective shipments by explaining that they monitor the “average” quality of all shipments, not the quality of each individual batch.

Further FDA Warnings Required Bayer to Remake Inaccurate Commercials To Properly Warn Users of the Risks: The FDA accused Bayer of misleading consumers in their extensive advertising campaigns in television and elsewhere by overstating the benefits of Yaz and Yasmin and failing to properly warn users about the extremely serious side effects of these drugs in comparison to other birth control pills on the market. As a result, the FDA issued two warning letters to Bayer in 2003 and 2008.

Elevated Potassium: The hormone in Yaz, known as drospirenone, raises potassium levels. Dangerously high levels of potassium can cause numerous health issues such as heart attack, heart arrhythmias, deep vein thrombosis, blood clots, stroke, and heart attacks, all of which are known to be potential side effects of Yaz.

Yaz (Yasmine/Ocella) Serious and Deadly Side Effects Include:

• potentially fatal blood-clots

• deep vein thrombosis (DVT),

• pulmonary embolism (PE),

• strokes

• heart attacks

• gallbladder problems (cholecystitis)

• gallbladder removal (cholecystectomy),

• kidney failure or renal failure

• pancreatitis

• organ failure

• sudden death

If you or your family member has experienced blood clots, heart attack, stroke, gall bladder condition or other serious injury from taking Yaz (Yasmine/Ocella), you may be entitled to compensation for your medical bills and for your pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

Related Posts:

Yaz Recall

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Yaz Risks

dom — Fri, 25 Feb 2011 21:23:03 +0000

LAWSUIT INFORMATION:

IF YOU OR YOUR LOVED ONE BEEN INJURED BY YAZ, YOU MIGHT BE ENTITLED TO FINANCIAL COMPENSATION. LET OUR LEGAL TEAM HELP YOU GET THE JUSTICE YOU DESERVE. CALL US NOW AT 1-888-736-4248.

Depending on your particular case, if a dangerous drug has harmed you, you may qualify for large financial compensation for such things as:

- your medical bills,
- your lost wages,
- your pain and suffering.
- punitive damages

ACT NOW TO FIND OUT IF YOU QUALIFY. CONTACT US AT 1-888-736-4248.

The first step is to contact our team of experienced drug recall attorneys right away so that we can let you know if you have a case.

Yaz and Yasmin (also marketed under generic Ocella, and Gianvi , Beyaz, Zarah , Safyral)

Generic Name: Drospirenone, Ethinyl estradiol

Yaz is a birth control pill, also known as oral contraceptive, that is currently among the most widely used in the U.S. It is made with active ingredient ethinyl estradiol and the new “fourth generation” progestin, or progesterone, drospirenone (DRSP). These birth control drugs have been promoted for use by young women (over 14 who have had their first menstrual period) to prevent pregnancy, reduce acne, regulate and minimize periods, and the symptoms associated with them (premenstrual dysphoric disorder).

Side Effects

The use of Yasmin and Yaz may cause a patient to experience certain side effects. In most cases these side effects will not be serious. Several of the common side effects associated with the use of Yaz or Yasmin are:

Breast pain or tenderness

Nausea

Weight gain

Vomiting

Breakthrough bleeding during menstrual periods

If you have experienced adverse side effects from taking YAZ (Yasmine/Ocella), [Heart attack, stroke, blood clots, gall bladder condition or other serious injury or death] you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

YAZ BLACK BOX WARNING:

FDA Black Box Warning Issued on Yaz: Yaz has been “black-boxed” by the F.D.A (strongest warning meant to call attention to possibly deadly or very serious side effect risks) warning consumers of the elevated risk of cardiovascular side effects, such as blood clots, strokes and heart attacks in patients who smoke while taking the medicine. The warning states that this risk increases with age and for woman over 35 who smoke 15 or more cigarettes daily.

YAZ SERIOUS AND DEADLY SIDE EFFECTS

Though these side effects are rare, those taking Yaz should be aware that there is a risk of experiencing the following:

• potentially fatal blood-clots

• deep vein thrombosis (DVT)

• pulmonary embolism (PE)

• cardiac arrhythmias

• strokes

• heart attacks

• gallbladder problems (cholecystitis)

• gallbladder removal (cholecystectomy)

• kidney failure or renal failure

• pancreatitis

• organ failure

• sudden death

Risk Factors

Certain women such as those who are both over 35 and are heavy smokers (15 or more cigarettes a day) are at a greater risk of experiencing certain severe side effects associated with Yaz, including adverse cardiovascular effects (blood clots, heart attack and stroke), increased potassium levels, liver tumors, and breast cancer.

Additional precautions should be followed as there is increased risk of side effects for those with the following conditions:

• Jaundice

• Blood-clotting disorders

• Obesity

• High blood pressure

• Diabetes

• Migranes

• Severe chest pains

• Liver tumors

• High cholesterol

Drug Interactions

Those taking Yaz (Yasmin/Ocella) may experience additional adverse reactions when taking them with certain medications, including prescription drugs, over-the-counter drugs, and supplements. Drugs that increase potassium levels may negatively interact with the hormone in Yaz and Yasmin, causing a patient’s potassium levels to increase to dangerous levels. Potassium-increasing medications that may react negatively with Yaz (Yasmin/Ocella) include:

• Potassium-sparing diuretics (spironolactone)

• Potassium supplements

• Non-steroidal anti-inflammatory drugs (pain relievers), for example ibuprofen and naproxen, if taken daily or for extended time periods

• Angiotensin-converting enzyme (ACE) inhibitors (e.g. Capoten, Vasotec, Zestril)

• Angiotensin-II receptor antagonists (e.g. Cozaar, Diovan, Avapro)

• Aldosterone antagonists

• Heparin

Yaz Lawsuit

dom — Fri, 25 Feb 2011 20:40:55 +0000

Yaz Lawsuit Information.

Yaz and Yasmin (also marketed under generic Ocella, and Gianvi , Beyaz, Zarah , Safyral). Yaz is a new version of Yasmin, which was originally approved for use in the U.S. in 2001; Ocella is the generic brand of the drug.

ONGOING CLASS ACTION LAWSUIT IN U.S.

Serious and sometimes deadly side effects associated with the use of Yaz have, as of early 2011, prompted over 6000 women to bring claims against Bayer Pharmaceuticals, the maker of Yaz, alleging injuries, and seeking to received compensation for their medical bills, lost wages, pain and suffering, among other damages suffered. Among the many claims against Bayer is that they failed to notify the public about the extent of the risks associated with the use of the drug. There is a Yaz class action lawsuit, where multiple plaintiffs with similar injuries against Bayer Pharmaceuticals group their legal claims together in bringing their lawsuit.

Some injured by Yaz are unsure where to turn, asking: Do I have a Yaz claim? What are the settlements for Yaz injuries? Can I sue for my Yaz use? What kind of financial award can I get with a Yaz lawsuit? Are there time limits for a Yaz case to be filed?

If you have experienced adverse side effects from taking YAZ (Yasmin/Ocella), [Heart attack, stroke, blood clots, gall bladder condition or other serious injury or death] you may be entitled to financial compensation to cover your medical bills, lost wages, pain and suffering. For a free case evaluation, please fill out the form on this page or call 888-736-4248.

Yaz (Yasmin/Ocella) (Prospirenone)

Class action suits pending. Over 6000 Lawsuits Filed As of 2011. There has been a huge increase in the number of Yaz (Yasmine/Ocella) lawsuits filed in the U.S. over the past year as the number of lawsuits filed has now surpassed 6000 as of January 2011. Only a year ago, according to the annual report of Bayer, the drug’s manufacturer, there were only 1100 filed, and as of October 2009, there had only been 129 filed. Currently, however, as of January 2011, there had been 5353 cases filed in the Illinois MDL (MDL #2100 in RE: Yasmin/Yaz (Prospirenone) Marketing, Sales Practices and Products Liability against Bayer or related entities, and over 765 filed in the New Jersey mass tort litigation. Majority of the claims are for damages related to blood clots, heart problems, strokes, pulmonary embolism or gallbladder conditions.

ANYONE WHO HAS EXPERIENCED ANY OF THE FOLLOWING SEVERE SIDE EFFECTS FROM THE USE OF YAZ (YASMIN/OCELLA) MAY BE ENTITLED TO RECEIVE FINANCIAL COMPENSATION BY FILING A LAWSUIT:

• potentially fatal blood-clots

• deep vein thrombosis (DVT)

• pulmonary embolism (PE)

• cardiac arrhythmias

• strokes

• heart attacks

• gallbladder problems (cholecystitis)

• gallbladder removal (cholecystectomy),

• kidney failure or renal failure

• pancreatitis

• organ failure

• sudden death

Related Posts:

Yaz Risks

Yaz Side Effects

Nuvaring Side Effects

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Ocella Recall

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Divalproex Sodium Side Effects

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Depakote Side Effects

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Darvon Side Effects

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Lentogesic Side Effects

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Di-Gesic Side Effects

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Dextropropoxyphene Side Effects

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Darvocet-N Side Effects

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Capadex Side Effects

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Darvocet Side Effects

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Rosuvastatin Side Effects

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Crestor Side Effects

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Proquin Side Effects

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Prociflor Side Effects

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Ciproxin Side Effects

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Ciprofloxacin Side Effects

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Cipro XR Side Effects

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Ciloxan Side Effects

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Ciflox Side Effects

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Baycip Side Effects

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Cipro Side Effects

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Varenicline Side Effects

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Champix Side Effects

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Chantix Side Effects

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Myfortic Side Effects

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Mycophenolic Acid Side Effects

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CellCept Side Effects

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Exenatide Side Effects

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Byetta Side Effects

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Dysport Side Effects

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Botulinum Toxin Side Effects

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Botox Side Effects

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Valdecoxib Side Effects

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Bextra Side Effects

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Vigamox Side Effects

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Moxifloxacin Side Effects

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Avelon Side Effects

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Avalox Side Effects

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Rosiglitazone Side Effects

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Avandaryl Side Effects

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Avandamet Side Effects

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Avandia Side Effects

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Salofalk Side Effects

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Rowasa Side Effects

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Pentasa Side Effects

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Mezavant XL Side Effects

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Mesalazine Side Effects

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Mesalamine Side Effects

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Lialda Side Effects

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Ipocal Side Effects

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Canasa Side Effects

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Apriso Side Effects

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Asacol Side Effects

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Viani Side Effects

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Seroflo Side Effects

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Seretide Side Effects

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Salmeterol Side Effects

dom — Wed, 23 Feb 2011 17:48:15 +0000

Here goes the text about the side effects of this drug.

Foxair Side Effects

dom — Wed, 23 Feb 2011 17:47:09 +0000

Here goes the text about the side effects of this drug.

ForAir Side Effects

dom — Wed, 23 Feb 2011 17:33:22 +0000

Here goes the text about the side effects of this drug.

Fluticasone Side Effects

dom — Wed, 23 Feb 2011 17:32:35 +0000

Here goes the text about the side effects of this drug.

Adoair Side Effects

dom — Wed, 23 Feb 2011 17:31:20 +0000

Here goes the text about the side effects of this drug.

Advair Side Effects

dom — Wed, 23 Feb 2011 17:30:22 +0000

Here goes the text about the side effects of this drug.

Sotret Side Effects

dom — Wed, 23 Feb 2011 17:28:17 +0000

Here goes the text about the side effects of this drug

Roaccutane Side Effects

dom — Wed, 23 Feb 2011 17:27:19 +0000

Here goes the text about the side effects of this drug.

Oratane Side Effects

dom — Wed, 23 Feb 2011 17:26:14 +0000

Here goes the text about the side effects of this drug.

Izotek Side Effects

dom — Wed, 23 Feb 2011 17:23:30 +0000

Here goes the text about the side effects of this drug.

Isotrex Side Effects

dom — Wed, 23 Feb 2011 17:22:31 +0000

Here goes the text about the side effects of this drug.

Isotrexin Side Effects

dom — Wed, 23 Feb 2011 17:21:40 +0000

Here goes the text about the side effects of this drug.

ISOTRET Side Effects

dom — Wed, 23 Feb 2011 17:19:52 +0000

Here goes the text about the side effects of this drug.

Isotane Side Effects

dom — Wed, 23 Feb 2011 17:18:32 +0000

Here goes the text about the side effects of this drug.

Decutan Side Effects

dom — Wed, 23 Feb 2011 17:17:33 +0000

Here goes the text about the side effects of this drug.

Clarus Side Effects

dom — Wed, 23 Feb 2011 17:16:51 +0000

Here goes the text about the side effects of this drug.

Claravis Side Effects

dom — Wed, 23 Feb 2011 17:15:02 +0000

Here goes the text about the side effects of this drug.

Amnesteem Side Effects

dom — Wed, 23 Feb 2011 17:12:29 +0000

Here goes the text about the side effects of this drug.

Yaz Side Effects

dom — Wed, 23 Feb 2011 02:41:08 +0000

Yaz (Yasmine/Ocella) Serious and Deadly Side Effects Include:

• potentially fatal blood-clots

• deep vein thrombosis (DVT),

• pulmonary embolism (PE),

• strokes

• heart attacks

• gallbladder problems (cholecystitis)

• gallbladder removal (cholecystectomy),

• kidney failure or renal failure

• pancreatitis

• organ failure

• sudden death

Related Posts:

Yaz Recall

Teen Girl Drops Dead From Birth Control Pill

Drospirenone

dom — Tue, 22 Feb 2011 18:10:00 +0000

Here goes the text about the Drospirenone recall.

Yasminelle®

dom — Tue, 22 Feb 2011 18:08:56 +0000

Here goes the text about the Yasminelle recall.

Yasmin®

dom — Tue, 22 Feb 2011 18:07:45 +0000

Here goes the text about Yasmin® side effects.

Yaz®

dom — Tue, 22 Feb 2011 18:05:10 +0000

If you have been a victim of Yaz (generic name: Rosiglitazone) and have suffered serious injury as a result of taking it, please contact JD Law Group immediately at 1-888-736-4248 to discuss your legal rights and options.

You may need an attorney specializing in the drug Yaz if you have suffered any of the serious side effects of the drug described further below.

Yaz is a type of birth control formula that contains drospirenone, which is essentially a synthetic progestin present in the birth control. Yaz is different from the various other forms of synthetic progestins as it is actually closer in makeup to natural progesterone. Because of this close pharmacological makeup, it may give users less breast tenderness and water retention while reducing the instance of acne. Yaz has also been used for the treatment of premenstrual dysphoric disorder and moderate acne.

Yaz is part of newer formulations of oral contraceptives. It contains 20 mcg of ethinylestradiol and 3 mg of drospirenone per tablet and it is used for contraceptive purposes. This contraceptive comes in a 24/4 style dosage, which means that the initial 24 pills will be active and contain the drospirenone and the last four pills will actually be placebo pills. Yaz works to change the uterine and cervical lining. This change prevents the sperm from reaching the uterus, as well as prevents fertilized eggs from attaching to the lining of the uterus. When Yaz is used according to the instructions, it is 99% effective in the prevention of pregnancy. However, that prevention does come at some risk.

Adverse Reactions to Yaz:

Yaz does have the potential for adverse reactions. Many of them are quite serious. These side effects can include the following:

· Decreased sex drive
· Spotting or bleeding between periods
· Headaches
· Nausea
· Vomiting
· Increased appetite
· Weight gain
· Vaginal discharge
· Yeast infections

More Serious Side Effects of Yaz:

Arrhythmias have been developed by women taking Yaz. These are characterized by chest pain, fatigue, sweating, feeling anxious, and dizziness, fluttering in the chest or neck, palpitations, lightheadedness, shortness of breath and loss of consciousness. Severity of the arrhythmia will ultimately determine the type of treatment necessary, as well as other factors including age and medical history. Some serious arrhythmias require pacemakers or other implant devices, medications and surgeries, while many can be treated by reducing caffeine, nicotine and alcohol and introducing stress reduction and relaxation techniques into the lifestyle. There is no known cure for an arrhythmia.

Any woman who develops any of the severe symptoms mentioned above should discontinue Yaz and seek medical attention immediately to ensure that their health and well being are secure.

If you have experienced serious side effects as a result of taking Yaz/Rosiglitazone, a lawyer with experience in the ongoing Rosiglitazone litigation can help evaluate your claim at no charge. The Yaz recall attorneys at JD Law Group are qualified to review your claim. You can contact them directly via 1-888-736-4248 or by filling out the contact form at the bottom of this page.

Salmeterol

dom — Tue, 22 Feb 2011 04:22:32 +0000

Here goes the text about the Salmeterol recall.

Fluticasone

dom — Tue, 22 Feb 2011 04:19:42 +0000

Here goes the text about Fluticasone recall.

Advair®

dom — Tue, 22 Feb 2011 04:18:15 +0000

Here goes the text about Advair® recall.

Isotretinoin

dom — Tue, 22 Feb 2011 03:25:43 +0000

Here goes the text about Isotretinoin side effects.

Side Effects of Accutane®

dom — Mon, 21 Feb 2011 21:43:14 +0000

Scientific data has linked Accutane® use to the development of inflammatory bowel disease, ulcerative colitis and Crohn’s Disease in some patients. In fact, before it was pulled from the U.S. market in 2009, the FDA required Hoffmann-La Roche to change the label to include a warning about the increased risk of inflammatory bowel disease. If you or someone you love has been diagnosed with inflammatory bowel disease and have a history of taking the acne medication, you might qualify for compensation.