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FDA Assessment FDA found insufficient evidence supporting intravenous emideltide for opioid withdrawal and no evidence supporting the nominated subcutaneous route

[DOI] [PubMed] [Google Scholar] 24.Hunjan MK, Evered DF

In the NEJM Phase 2 trial, participants assigned to an initial dose of 4 mg experienced significantly more adverse events than those who started at 2 mg, even when both groups ultimately reached the same target dose

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it seems to have reduced the size of my legs a little bit and thats the only change so far

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