FDA advisers to decide on continued sale of 2 pain drugs

An FDA panel is expected to decide today whether painkillers Darvon and Darvocet should be pulled from the market because of concerns about their addictive effects. The drugs contain propoxyphene, which has been linked to 3,028 cases of adverse events between 1957 and Sept. 24, 2008, according to the FDA. The agency sought advice from independent experts in response to a petition and lawsuit from advocacy group Public Citizen.

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This story published in FDLI SmartBrief on 01/30/2009





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