Avandia (Rosiglitazone) Side Effects Lawsuit News:

More FDA Corruption

-AlterNet

03/08/2010 - FDA and Avandia a diabetes drug linked to 83,000 heart attacks. The FDA’s own research showed Avandia to be associated with a significant increase in heart attack risk, and yet the FDA did nothing to protect the public. The AMA admitted Avandia was dangerous. In its journal “Among patients with impaired glucose tolerance or type 2 diabetes, rosiglitazone (avandia) use for at least 12 months is associated with a significantly increase risk of myocardial infarction.” The New England Journal of Medicine also warned about the safety of the drug. Despite these multiple warnings, an FDA panel voted 22-1 in favor of keeping Avandia on the market. When it comes to safety vs. profits, the FDA chooses profit for BigPharma time and time again.

Then there is the case of Dr.Scott Reuben, who published fake studies on drug research for 13 years published in major medical journals. His research proving the efficacy of celebrex helped reduce pain during post-surgical recovery, had one problem there were no patients enrolled in the study. Dr. Rueban faked the entire study. Where was the FDA when all this was going on? Then his faked studies on Vioxx and Bextra. FDA panel members regularly rely on falsified reports, and that is how the FDA protects the public.

Avandia Side Effects Class Action Lawsuit Cases Still Being Accepted:

The lawyers of Ennis & Ennis, P.A. are still accepting Avandia side effects cases and have extensive experience representing plaintiffs in Avandia lawsuits nationwide.