Emails Confirm GlaxoSmithKline Concealed Avandia Injury Concerns

A series of e-mails confirm what medical injury lawyers have suspected for months now - that GlaxoSmithKline has been long aware of the side effects associated with the use of its diabetes medication, Avandia.

In 2007, a study by pioneering Cleveland Clinic cardiologist Dr. Steven Nissen, published in the New England Journal of Medicine, revealed that patients who took Avandia are at a higher risk of developing cardiac disease. Doctor Nissen studied the effects of Avandia use in more than 15,000 patients, monitoring 12,283 subjects in a control group. He found 86 cases of myocardial infarction in the group that was given Avandia, compared to 72 cases in the control group, and 39 deaths among Avandia users as opposed to 22 deaths in the control group. At the time, Dr. Nissen acknowledged that a few deaths in more than 15 thousand subjects may seem like an inconsequential number, but because the studies were conducted over a short period of time and because of the increased risk of heart disease in diabetic patients, the enhanced incidence of heart attacks in Avandia users was cause for worry. Glaxo was quick to refute the findings of the study. The company released a statement questioning the methods used by Dr. Nissen, but the FDA quickly issued a safety alert on Avandia.

Since then, the link between Avandia and heart disease has become stronger with more numbers of people killed and hundred of cases of heart failure. Now, reports indicate that the company was aware of the increased risk all along. According to reports, senior GlaxoSmithKline scientists wrote e-mails just before the publication of Doctor Nissan's study admitting that his findings were "very similar" to the conclusions reached by GlaxoSmithKline. The company, at the time, was under scrutiny because of the Vioxx scandal which associated Merck's painkiller with an increased risk of heart disease. The Vioxx concerns ended with the company withdrawing the drug and hundreds of medical injury lawsuits filed by patients who suffered heart attacks after taking Vioxx.  Desperate to avoid Merck's fate, Glaxo went all out to criticize Dr. Nissen's findings almost immediately after publication of the study. Avandia use has decreased dramatically since then, but it remains on the market and thousands of patients continue to take the drug.

Pursuing Medical Injury Claims

Pharmaceutical companies may often hide important safety information about their drugs in order to remove obstacles in their marketing plan. Such suppression of information may be grounds for a medical injury lawsuit against the drug maker in the event of injuries caused by the drug.

If you or a loved one have suffered heart problems after taking Avandia, you may have grounds for compensation. Contact the medical injury lawyers at Arnold & Itkin LLP for a free evaluation of your case.

 

Diabetes drug Byetta linked to injuries and death

Deaths have been reported in connection with the widely used diabetes drug, Byetta (exenatide), marketed by Amylin Pharmaceuticals and Eli Lilly & Co.  An alert from the FDA said they have received reports of 6 cases of hemorrhagic or necrotizing pancreatitis in patients taking Byetta.  Byetta is a medicine given by subcutaneous injection to help treat adults with type 2 diabetes. Of the 6 cases of hemorrhagic or necrotizing pancreatitis, all patients required hospitalization, two patients died and four patients were recovering at the time of reporting.  Byetta was discontinued in all 6 cases. Federal regulators are working on a stronger label fo the drug.

If you or a loved one have been seriously injured by a defective pharmaceutical drug like Byetta, you may be entitled to compensation from those responsible for your injury. Contact the medical injury lawyers at the Arnold & Itkin LLP law firm in Houston, Texas to learn more about your options.