Curt Furberg, a professor at Wake Forest University, has been removed from an FDA advisory panel set to review the safety of COX-2 inhibitors next year, after he publicly questioned the safety of Pfizer's Bextra, the Wall Street Journal reports. Preliminary results of a University of Pennsylvania study presented on Tuesday at the American Heart Association annual conference in New Orleans indicated that Bextra doubles patient risk for heart attack and stroke. Furberg said FDA informed him that he would no longer participate in a committee meeting next year to review the safety of COX-2 inhibitors, including Bextra, Pfizer's Celebrex and Merck's Vioxx, after he was quoted in the New York Times as saying Bextra appeared to have similar risks to Vioxx -- which was withdrawn from the market in September for safety reasons -- and Pfizer tried to conceal that information. The FDA meeting on COX-2 inhibitors is scheduled for mid-February.
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