The US consumer group Public Citizen has sued the Food and Drug Administration for failing to act on its petition to withdraw Darvon, Darvocet and all other drugs containing propoxyphene gradually from the market as has now been required in the UK.
The group's complaint, filed in the US District Court for the District of Columbia, argues that the FDA is violating the law by not acting on Public Citizen's February 28, 2006, petition. By not doing so, the agency is allowing drugs containing propoxyphene to remain on the market, putting patients at risk, it says.
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