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View Diary: White House task force reviewing gun violence options pushes to meet end of month deadline (235 comments)

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  •  FDA ordered Darvon and Darvocet (1+ / 0-)
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    glorificus

    Manufacturers to recall these meds as studies proved beyond any doubt their use was associated and contributed to users developing atrial fibrillation (irregular heart rhythm, which can be fatal).  And the FDA had these studies for some years and kept quiet on any action.  Which is why the manufacturers and the FDA are named in lawsuits.  Hope this answers your question.

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