FDA Panel on Drug-Eluting Stents - Day 2
Saturday December 9, 2006
Yesterday, in its second of 2 days of deliberation, the FDA's Circulatory Systems Devices Advisory Panel on drug-eluting stents (DES) considered what recommendations to make regarding the off-label usage of DES.
In general, the panel agreed that the risk of late thrombosis with DES is higher when these stents are used for off-label indications than when used for on-label indications, and that, at least for patients at highest risk for stent thrombosis, the off-label use of DES should be curtailed to at least some degree.
Click here for more details on the FDA panel's deliberations.


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