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Step 2: Provider review and prescription

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And the agency has warned about companies illegally selling unapproved products containing semaglutide, tirzepatide or retatrutide falsely labeled "for research purposes" or "not for human consumption." As of May 31, 2026, the FDA had received 990 adverse event reports associated with compounded semaglutide and more than 730 associated with compounded tirzepatide