EMEA confirms withdrawal recommendation for dextropropoxyphene

This article was originally published in SRA

30 Oct 2009
News

Ian Schofield @ScripIanS ian.schofield@informa.com

Executive Summary

The European Medicines Agency has recommended that all non-parenteral forms of medicines containing the analgesic dextropropoxyphene be withdrawn because their risks – particularly the possibility of fatal overdose – outweigh their benefits¹.

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EMEA confirms withdrawal recommendation for dextropropoxyphene

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