On Friday, the FDA announced that the maker of Darvon (and the similar drug, Darvocet) has voluntarily stopped all marketing of the drugs in the United States. Both drugs have been accused of causing deadly side-effects for decades. The reason for the current recall: A cardiac study conducted by the manufacturer at the FDA’s bequest showed that Darvon caused irregular heart rhythms. In other words, the doses of Darvon and Darvocet normally prescribed by doctors and taken by patients is harmful to the heart. Couple this with the unacceptable propensity of patients to abuse the drug (i.e., taking more than the prescribed amount) and the risk of heart damage is simply too great to keep the drug on the market.
This recall follows bans in England and the European Union based on a different reason: The long-held belief that the use of Darvon and Darvocet lead to unacceptable risks of suicides and overdoses. Many safety advocates in the U.S. have been calling for the ban of these drugs since at least 1978, but the FDA has refused until now.
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