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Additionally, the agency has received adverse event reports that may be related to patients prescribed compounded semaglutide or tirzepatide products in doses beyond what is in the FDA-approved drug label

10.1111/1759-7714.12783 168 UehiroN.SatoF.PuF.TanakaS.KawashimaM.KawaguchiK.et al (2016)

Of note, only small number of sudies investigated this outcome with heterogenity in inclusion criteria among study populations, and differences in AOX combinations and SDF assays used

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