FDA Advisory Panel to Review Data Regarding Safety of Avandia

CNN (7/9, Hellerman) reported that, “A decade after critics first accused the Food and Drug Administration of downplaying side effects from Avandia (rosiglitazone), the agency says it will reveal on Friday the data it is reviewing ahead of an advisory panel meeting about the safety of the popular diabetes drug.” The meeting is scheduled for July 13 and 14, and follows  two new studies suggesting that Avandia may cause serious or even life-threatening heart problems — and a third study that seems to show just the opposite.”

An editorial in the USA Today (7/9) stated, “Since 2005, evidence has mounted that the blockbuster diabetes drug Avandia (rosiglitazone maleate) might increase the risk of cardiovascular complications — including heart attacks, one of the major causes of death among diabetics.”