Accutane Side Effects – Suicide, Birth Defects, Inflammatory Bowel Disease

Accutane Side Effects Drug Toxic Chemicals

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Accutane Side Effects – Suicide, Birth Defects, Inflammatory Bowel Disease

Accutane, a synthetic form of vitamin A used to treat severe acne, has been the subject of much controversy and litigation due to serious side effects including severe inflammatory bowel disease, birth defects, suicide, depression, psychiatric disorders, and the potential for violence in patients taking it, as well as a long list of less serious side effects.

Patients have reported both inflammatory bowel disease and lupus after using Accutane. Some possible symptoms to watch for are:

Stomach, chest, or bowel pain

Rectal bleeding or serious or bloody diarrhea

Pain or difficulty swallowing

Increased heartburn

Yellowing of the skin or eyes

Dark urine

Bad headache or dizziness

Nausea and vomiting

Joint or muscle pain

Bone problems

Hearing loss

Difficulty breathing

Fainting

Increased thirst or urination

Slurred speech

Difficulty moving

Leg swelling

Increased cholesterol or triglycerides in blood

If you suffer these side effects you should seek medical help immediately. Blood levels of cholesterol and triglycerides should be monitored during treatment with Accutane.

There have also been reports of suicides, suicidal thoughts, and other psychiatric disorders in patients taking Accutane since 1985. The FDA has required stronger warning on several occasions. Symptoms of these problems can include:

Depression

Sadness

Irritability

Unusual fatigue

Difficulty concentrating

Change of sleep patterns

Loss of appetite

Suicidal thoughts

Suicide attempts

Seizures

Patients taking Accutane should be carefully monitored for these symptoms and should contact a health care provider immediately if they occur.

The harm to infants whose mothers have taken Accutane during the pregnancy or shortly before getting pregnant is so clear that both the manufacturer, Hoffman La Roche, and the FDA (Food and Drug Administration) have worked to create programs to make sure that patients taking the drug do not become pregnant. These efforts have not been successful and both pregnancies and birth defects continue to occur.

Suffered harm from Accutane? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

At least one study has also linked Accutane to increased levels of tryglycerides, cholesterol, and transaminase. Less serious potential Accutane side effects include:

Increased risk of sunburn

Increased risk of scarring

Decreased night vision

Accutane should not be taken with several kinds of other medications, which might increase the risks of side effects. You should tell your health care providers all the medications and supplements you’re taking before deciding to take Accutane. With all the concerns about birth defects and emphasis on birth control, you should be aware that Accutane may interfere with the effectiveness of birth control pills that do not contain estrogen.

Check out the following articles for more information about Accutane, filing an Accutane lawsuit and finding an Accutane attorney.

For more information about Accutane, see Drug Overview: Accutane Side Effects and Claims.

For more information about Accutane updates, see Accutane Information and Warnings.

If you would like to learn more about Accutane lawsuits, see Accutane Lawsuits, Litigation & Lawyers.

To learn more about Accutane attorneys and how to find one, see Hiring an Accutane Attorney and Lawyer

Suffered harm from Accutane? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

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Accutane: Drug Overview

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Accutane: Drug Overview

Accutane (generic isotretinoin) is a form of synthetic vitamin A used to treat serious forms of cystic acne that will not respond to other treatment. The Accutane claim is that it sometimes permanently clears serious acne after a few months of treatment, while other treatments are only effective as long as they are continued. Accutane decreases the amount of oil (sebum) produced by the oil (sebaceous) glands in the skin and increases the rate at which the skin is renewed.
Suffered harm from Accutane? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.
Accutane is manufactured in the US by Hoffman La Roche, part of “The Roche Group,” a leading international pharmaceutical company with subsidiaries active in 150 countries. Accutane was approved by the FDA (Food and Drug Administration) in June 1982, and by 2000 Hoffman La Roche reported that 5 million people in the US and 12 million worldwide had taken the drug, most of them young adults.
Within a year of the FDA’s approval reports began to come in of serious deforming birth defects in children born to women using Accutane. Within 3 years of the FDA approval reports, other alarming side effects, including depression and seizures, began to come in. There were reports of several suicides in patients taking Accutane. Later reports of severe cases of inflammatory bowel disease and pancreatitis were reported.
The FDA has required several increased levels of warnings about side effects and Hoffman La Roche has designed two programs to reduce the number of pregnancies in women using Accutane that were not successful, followed by an equally unsuccessful FDA program.
Check out the following articles for more information about Accutane, filing an Accutane lawsuit and finding an Accutane attorney.
For more information about Accutane side effects, see Accutane Side Effects – Inflammatory Bowel Disease, Suicide & Birth Defects .
For more information about Accutane updates, see Accutane Information and Warnings.
If you would like to learn more about Accutane lawsuits, see Accutane Lawsuits, Litigation & Lawyers.
To learn more about Accutane attorneys and how to find one, see Hiring an Accutane Attorney and Lawyer
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Is Social Security counted as income in the means test under the new bankruptcy law?

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Is Social Security counted as income in the means test under the new bankruptcy law?

No. Social security payments are excluded from the calculation of income for purposes of the means test.
Some consumer bankruptcy lawyers believe that unemployment compensation derives from the Social Security Act and should also be excluded from Current Monthly Income.
(Reviewed 11.14.08)

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Accutane – New Study Reveals Increased Risks for Heart and Liver Problems

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Accutane – New Study Reveals Increased Risks for Heart and Liver Problems

Accutane, is a synthetic form of vitamin A used to treat severe acne. Accutane, while an effective drug for the treatment of acne, has been linked to some serious potential side effects, including birth defects, suicide, depression, and psychiatric disorders.
Accutane has also been linked to higher levels of cholesterol, liver enzymes and blood fats called triglycerides. But a recent study, published in the Archives of Dermatology [correct link http://archderm.ama-assn.org/cgi/content/full/142/8/1016?maxtoshow=&HITS=10&hits=10&RESULTFORMAT=&fulltext=accutane&searchid=1&FIRSTINDEX=0&resourcetype=HWCIT], found elevated levels in a higher percentage of patients than expected. While the drug insert indicates high triglyceride levels in 25% of the patients who had normal lab tests before taking the drug, the new study found elevated levels in 44% of healthy patients. Thirty-one percent of the patients in the study developed high cholesterol and 11% developed abnormal liver tests.
Suffered harm from Accutane? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.
While the recent UCSF study reveals increased risks for Accutane patients, the risks do not appear to be serious enough to cause alarm. Dermatologists are expected to continue to closely monitor patients who take Accutane. Most lab results for patients who participated in the study returned to normal once the patients were off the medication.
Always talk to your doctor if you are at all concerned about any drug you are taking. More detailed information about earlier Accutane studies, warnings, lawsuits, and how to find an Accutane lawyer are provided in the articles listed below.
For more information about Accutane, see Drug Overview: Accutane Side Effects and Claims.
For more information about Accutane side effects, see Accutane Side Effects – Suicide, Birth Defects & Inflammatory Bowel Disease.
For more information about Accutane updates, see Accutane Information and Warnings.
If you would like to learn more about Accutane lawsuits, see Accutane Lawsuits, Litigation & Lawyers.
To learn more about Accutane attorneys and how to find one, see Hiring an Accutane Attorney and Lawyer.
Suffered harm from Accutane? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.
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Hiring An Accutane Attorney and Lawyer

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Hiring An Accutane Attorney and Lawyer

If you or a member of your family has been injured after using the acne medication Accutane, you may be able to get compensation for your injuries. It’s important that you find a qualified Accutane attorney to help you evaluate your case. If you decided to proceed with an Accutane lawsuit, you will need to find an experienced pharmaceutical litigation attorney. Even if you manage to settle your case before going to court, you will almost certainly get a better settlement if you are represented by an experienced Accutane lawyer. A knowledgeable lawyer can add value that far exceeds the cost of the lawyer’s fees.
Suffered harm from Accutane? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.
Your Accutane lawyer will know how to handle the specialized aspects of pharmaceutical litigation and will also be experienced in more procedural aspects of your case. Your state law sets out the time you have to bring a lawsuit to recover damages for your injuries. The timing usually depends on several factors, and an experienced attorney can help you file your case on time.
Your Accutane attorney will also help you decided which parties to name as defendants. For example, you may have a claim against your physician for malpractice if the physician didn’t tell you about the risks of associated with Accutane, but you may not have a claim against the manufacturer. Your lawyer will also know the best place to file your suit, since some courts tend to produce better results for plaintiffs than others.
So how do you find a good Accutane attorney? For most types of lawsuits, word of mouth is usually the best way. But drug liability is pretty specialized, and you may not know anyone who has sued a drug company, and even if you did, their experience is limited. A good place to start is AttorneyPages.com, where you’ll find listings for drug liability specialists in your area, or post your case to the free Case Evaluation Form. After posting your case, an experienced law firm that handles Accutane and similar cases will contact you for a free case evaluation, without any cost or obligation.
Check out the following articles for more information about Accutane, filing an Accutane lawsuit and finding an Accutane attorney.
For more information about Accutane, see Drug Overview: Accutane Side Effects and Claims.
For more information about Accutane side effects, see Accutane Side Effects – Suicide, Birth Defects & Inflammatory Bowel Disease.
For more information about Accutane updates, see Accutane Information and Warnings.
If you would like to learn more about Accutane lawsuits, see Accutane Lawsuits, Litigation & Lawyers.
Suffered harm from Accutane? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

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Accutane Lawsuits, Litigation & Lawyers

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Accutane Lawsuits, Litigation & Lawyers

The acne remedy Accutane, a synthetic form of vitamin A used to treat serious forms of acne that can cause scarring, has been the subject of extensive litigation because of a long list of side effects including inflammatory bowel disease, suicide, and birth defects.
Suffered harm from Accutane? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.
The U.S. manufacturer of Accutane, Hoffman La Roche, is part of the international conglomerate known as “The La Roche Group,” with affiliates in 150 countries. “The La Roche Group” is estimated to be the seventh largest pharmaceutical company in the world. Accutane is one of Hoffman La Roche’s top sellers with estimated annual sales of $1.2 billion. Accutane is also one of the 3 drugs on the market with the most reports of adverse side effects, and this has led to extensive litigation. Lawsuits have been brought against Hoffman La Roche for alleged adverse reactions caused by Accutane including gastrointestinal disorders, suicides, and birth defects.
In May of 2007, a man who suffered gastrointestinal harm received a judgment of $2.5 million against Roche. This was followed in October 2007 by a judgment for $7 million to a man who had his colon removed. Roche appealed the second judgment and it was upheld in February 2008. In April 2008, a 24-year-old woman who had part of her intestines removed won a $10 million verdict against Roche. Roche has vowed to appeal all judgments for injury caused by inflammatory bowel disease, claiming that the link between inflammatory bowel disease and Accutane has not been proven and that Roche has had a warning for the condition on the label for over 20 years.
Lawsuits about psychiatric side effects of Accutane include the following:
The family of Charles Bishop, a 15-year-old boy who crashed a small plane into a Tampa skyscraper after taking Accutane for 8 months.
The family of Steven Wertheimer, a 14-year-old who was killed when he stood in front of a commuter train next to the Palo Alto High School football field.
The family of a 22-year-old Virginia man who committed suicide.
The family of a 21-year-old woman who attempted suicide while taking Accutane.
Another suit against Hoffman La Roche was filed by a 33-year-old mother who suffered severe depression when she took Accutane and had a child with severe birth defects. At least one appeals court (New Jersey) has ruled, however, that Hoffman La Roche cannot be liable for birth defects caused by Accutane, because Hoffman La Roche has been warning both health care providers and patients about the risk for many years. Patients may still have claims against health care providers, clinics, or others who prescribed Accutane unnecessarily, did not warn of side effects, or did not monitor the patient adequately during treatment.
For more information about Accutane, see Drug Overview: Accutane Side Effects and Claims.
For more information about Accutane side effects, see Accutane Side Effects – Suicide, Birth Defects & Inflammatory Bowel Disease.
For more information about Accutane updates, see Accutane Information and Warnings.
To learn more about Accutane attorneys and how to find one, see Hiring an Accutane Attorney and Lawyer.
Suffered harm from Accutane? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

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Accutane Information and Warnings

Accutane Information Drug Toxic Chemicals

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Accutane Information and Warnings

Accutane, the trade name for the generic drug isotretinoin, is approved by the FDA for the treatment of cystic or nodular acne that can cause severe scarring. Because of serious and varied side effects, Accutane is recommended for use only when all other possible treatments have failed. Accutane is a synthetic form of vitamin A that decreases the amount of oil on the skin and increases the rate of skin replacement.
Suffered harm from Accutane? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights. Accutane has been linked to pancreatitis and inflammatory bowel disease. Increased suicidal thoughts and suicide attempts may also be Accutane side effects. These issues have been the subject of several lawsuits, See Accutane Lawsuits, Litigation & Lawyers for more information. Some of these lawsuits argue that Hoffman La Roche has withheld information about the danger of suicide and other psychiatrically related Accutane side effects. The FDA has required Hoffman La Roche to increase the level of warning about psychiatric disorders related to Accutane use in 1998, 2000, and 2002.
Hoffman La Roche, the manufacturer of Accutane, admits that Accutane causes birth defects in many children born to mothers who took Accutane during pregnancy or shortly before becoming pregnant. A 1990 FDA report estimated 11,000 to 13,000 Accutane-related abortions and 900 to 1,100 Accutane-related birth defects since the drug had been approved. Under pressure from consumer advocacy groups and the FDA, Hoffman La Roche has issued warnings of the danger of birth defects and set up programs intended to educate patients and reduce the number of women who become pregnant while taking Accutane.
A more recent study has linked Accutane to heightened levels of tryglycerides, cholesterol, and transaminase.
If your health care provider recommends treatment with Accutane, carefully consider the side effects, take every care not to become pregnant during the treatment, and make sure that you and your health care provider monitor your health for possible side effects.
If you or a family member have been injured or a family member has died after using Accutane, you may be entitled to receive compensation for your damages. Consult a qualified Accutane attorney to have your case evaluated.
Check out the following articles for more information about Accutane, filing an Accutane lawsuit and finding an Accutane attorney.
For more information about Accutane, see Drug Overview: Accutane Side Effects and Claims.
For more information about Accutane side effects, see Accutane Side Effects – Inflammatory Bowel Disease, Suicide, & Birth Defects .
For more information about Accutane updates, see Accutane Information and Warnings.
If you would like to learn more about Accutane lawsuits, see Accutane Lawsuits, Litigation & Lawyers.
To learn more about Accutane attorneys and how to find one, see Hiring an Accutane Attorney and Lawyer.
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Expert Says New Drugs May Be More Harmful Than Existing Ones

Experts Say New Drugs Maybe More Harmful Drug Toxic Chemicals

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Expert Says New Drugs May Be More Harmful Than Existing Ones

A New Jersey sociologist has reported that new drugs may be more harmful than existing drugs due to how clinical trials are conducted by drug companies and how the U.S. Food and Drug Administration (FDA) uses that data.
Newer isn’t always better
According to news reports, Donald Light, a sociologist and professor of comparative health policy at the University of Medicine and Dentistry of New Jersey, says that newer isn’t always better when it comes to drugs and that “fatal flaws” exist in the process of testing new drugs that may put consumers at risk of serious injury or death. In a study conducted by Light that will be presented at a future American Sociological Association meeting, he alleges that out of every seven new drugs that comes on the market, only one is superior to a similar existing drug and that two of the seven result in serious side effects which may lead the FDA to issue black box or other warnings or even to withdraw the drugs from the market altogether.
Why the process doesn’t work
According to Light’s study, there are two reasons why the process doesn’t work. The first is that clinical trials of drugs are compared to placebos instead of a similar, existing product, so as long as a drug works better than the placebo, it is considered “effective.” The second is that many drug manufactures conduct their clinical trials in ways that will “minimize” any adverse effects, such as not conducting trials for an appropriate amount of time to discover the drug’s true side effects. Light’s conclusions seem to agree with other studies.
The FDA bases much of its decision on whether to approve a drug on the clinical trials conducted by the manufacturer itself. Critics of the FDA’s procedures say that drug companies understand that the FDA is understaffed and under funded to adequately direct the process – especially with the staggering number of new drugs that seek approval every year.
Consumers pay the price
Unfortunately, consumers end up paying the price for the information not gathered before a drug is approved for use and many feel as though drug companies should be ultimately responsible for their products regardless of the FDA’s requirements or actions. If you’ve been injured due to a drug, contact a lawyer whose practice focuses in this area of the law to discuss your situation free of charge. There is no obligation and the consultation is strictly confidential. To contact one of our experienced lawyers, please click here. We may be able to help.

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Avandia Overview: Avandia Side Effects and Claims

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Avandia Overview: Avandia Side Effects and Claims

Avandia, generic rosiglitazone maleate, is a drug to treat Type 2 diabetes and is manufactured by the UK-based pharmaceutical giant GlaxoSmithKline (GSK). Type 2 diabetes is the most common form of diabetes, affecting about 18 million Americans. In Type 2 diabetes the body either does not produce enough insulin or does not use insulin properly. This results is high blood sugar levels that can cause problems such as kidney and eye damage. The Avandia claim is that it lowers blood sugar levels by increasing the sensitivity to insulin in peripheral tissue.
Avandia is the top-selling diabetes drug in the world and the second best seller for GSK, after its asthma drug Advair. It’s estimated that Avandia was taken by 1 million Americans in 2006 and generated $3 billion in sales. Avandia was approved by the FDA (Food and Drug Administration) on May 15, 1999 for the treatment of diabetes. There was some controversy about the approval, but the FDA may have wanted to expedite the approval since problems had already arisen with the other diabetes drug then on the market, Pfizer’s Rezulin. Rezulin was removed from the market in 2000 because it caused sometimes fatal liver problems.
Suffered harm from Avandia? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.
Avandia is part of a class of drugs known as PPAR agonists. These drugs activate or suppress dozens of genes, causing complex biologic effects. The effects differ from one PPAR agonist to another, depending on the genes affected.
Avandia hit the headlines on May 21, 2007 when a meta-analysis of 42 studies on the use of Avandia showed a significant increase in the risk of heart attack and other heart problems. See Avandia Information and Warnings for more information. The FDA eventually issued a warning about the study and required GSK to include a black box warning of cardiac side effects and to produce a new prescription guide that included these warnings. Critics claim the FDA should have acted sooner. The agency came under criticism and scrutiny for its handling of the Avandia approval and review. See Avandia Side Effects and Risks
Check out the following articles for more information about Avandia, filing an Avandia lawsuit and finding an Avandia attorney.
For more information about Avandia side effects, see Avandia Side Effects – Heart Attack and Fractures
To find out more about the FDA warning, see Avandia Side Effects and Risks
For more information about Avandia updates, see Avandia Information and Warnings
If you would like to learn more about Avandia lawsuits, see Avandia Lawsuits, Litigation & Lawyers
To learn more about Avandia attorneys and how to find one, see Hiring a Avandia Attorney and Lawyer
Suffered harm from Avandia? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

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Avandia Side Effects – Heart Attack

Avandia Heart Attack Drug Toxic Chemicals

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Avandia Side Effects – Heart Attack

An increased risk of heart attack and other cardiovascular problems have been linked to Avandia, GlaxoSmithKline’s best-selling drug for the treatment of Type 2 diabetes, in a recent meta-analysis. Because Avandia is used by approximately 1 million Americans, and because diabetes patients are particularly prone to heart attacks and cardiovascular difficulties, this potential risk is reason for serious concern.
A 2007 study found that women who take Avandia or the drugs Avandamet or Avandaryl, also manufactured by GlaxoSmithKline, have an increased risk of bone fractures, particularly in the upper arm, hand, or foot. Men taking these drugs don’t seem to be affected in this way. The active ingredient in the drugs causing this problem is rosiglitazone.
The following are identified as additional potential Avandia side effects:
Congestive heart failure
Pulmonary edema
Pleural effusion
Anemia
Swelling
Unexplained rapid weight gain
Trouble breathing
Unusual fatigue
Racing or pounding heartbeat
Dark urine
Yellowing of eyes or skin
Persistent nausea or vomiting
Stomach or abdominal pain
Suffered harm from Avandia? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.
Avandia has also been reported to worsen certain effects of diabetes, including:
New or worsening diabetic macular edema with decreased visual acuity
Hypergylcemic (high blood sugar level) effects
The symptoms of hyperglycemia include:
Thirst
Increased urination
Confusion
Drowsiness
Flushing
Rapid breathing
Fruity breath odor
Avandia has been reported to produce symptoms of hypoglycemia, or low blood sugar levels. Those symptoms include:
Chills
Cold sweats
Dizziness
Drowsiness
Shaking
Rapid heart rate
Weakness
Headache
Fainting
Tingling in the hands and feet
Hunger
Some patients are allergic to Avandia, and allergy symptoms can include:
Rash
Itching
Swelling
Dizziness
Trouble breathing
Suffered harm from Avandia? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.
The experts agree that patients currently taking Avandia should not stop taking the medication on their own, but they should consult with their health care providers to discuss alternate treatment possibilities. There are several drugs on the market for the treatment of diabetes that have not been linked to heart disease or bone fractures.
If you or someone close to you has suffered a heart attack or cardiovascular problems after taking Avandia, you should investigate the possibility that the injury was caused by Avandia. To find out if you might be eligible to file an Avandia lawsuit, you need to have your case evaluated by an experienced Avandia attorney. See Avandia Attorney and Lawyer – How to Hire to the right lawyer to help you.
Check out the following articles for more information about Avandia, filing an Avandia lawsuit and finding an Avandia attorney.
For more information about Avandia , see Drug Overview: Avandia Side Effects and Claims
To find out more about the FDA warning, see Avandia Side Effects and Risks
For more information about Avandia updates, see Avandia Information and Warnings
If you would like to learn more about Avandia lawsuits, see Avandia Lawsuits, Litigation & Lawyers
To learn more about Avandia attorneys and how to find one, see Hiring a Avandia Attorney and Lawyer
Suffered harm from Avandia? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.
Suffered harm from Avandia? You may have a lawsuit. Click here, for a top rated law firm to evaluate your legal rights.

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