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UPDATE NOVEMBER 2010: Nearly two years after this recommendation, the FDA announced the re of Darvocet and Darvon on 11/19/2010, indicating that data now links the medications to a potential risk of heart arrythmias, in addition to other side effects, such as suicide, overdose and death. Last week, an FDA advisory panel voted to recommend that a re of Darvon and Darvocet be issued due to the risk of death, overdose and addiction, outwehing the eminimal benefits provided by the drugs over other available painers. While the FDA is not required to follow the advice of their advisory panel, they usually do.

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Ultram and darvocet:

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