Beasley, Allen, Crow, Methvin, Portis & Miles, P.C.

It’s a long time coming. This week the Food and Drug Administration (FDA) announced it is reviewing the primary data from a large, long-term clinical study, known as RECORD, on possible cardiovascular risks associated with the diabetes drug Avandia (rosiglitazone). The agency said it is also reviewing on an ongoing basis a number of other published observational studies on the cardiovascular safety of the drug. The FDA’s announcement comes on the heels of news that two U.S. senators are asking why the GlaxoSmithKline (GSK) drug is still on the market when an FDA oversight board in 2008 urged the agency to pull the drug because it was causing 500 additional heart attacks a month. That request by the oversight board was based on the findings from the RECORD study.

Read the rest of this entry »

Two U.S. senators are asking the Food and Drug Administration (FDA) why the diabetes drug Avandia is still on the market after an agency oversight board in 2008 urged the agency to remove the GlaxoSmithKline (GSK) drug from the market because it was causing 500 additional heart attacks a month. Senators Max Baucus and Charles Crassley said the major drug company even knew about the dangers of Avandia but initiated a cover up to keep the drug available to consumers.

Read the rest of this entry »