MONDAY, July 30 (HealthDay News) -- The widely prescribed type 2
The U.S. Food and Drug Administration advisory panel voted 22-1
to keep the drug on the market, although it recommended Avandia
should carry new
"The committee felt, almost uniformly, that there is a risk to
some patients," said Dr. Clifford Rosen, the acting committee
chairman from the Maine Center for
"There was some increased risk of cardiac events to some patients. The signal for increased risk was there, with some qualifications," he told reporters at a teleconference.
Patients at risk include those with
But the decision to keep the drug on the market, according to an FDA official, came about because the committee wasn't convinced that the data presented about the risk was conclusive.
"If we have a clear answer, we don't take this to an advisory committee," Dr. Robert Meyer, the director of the FDA's Office of Evaluation II, Center for Drug Evaluation and Research, told reporters.
Dr. Gerald Dal Pan, director of the FDA's Office of Surveillance
and Epidemiology, said, "We will go back and formulate what we
think should be on the label." Panelists' suggestions included a
black box warning or other warning for
The FDA had previously asked the drug's manufacturer, GlaxoSmithKline, to add a black box warning about heart failure.
While the FDA isn't bound to follow the recommendations of its advisory panels, it typically does so.


















