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This was higher than the 8.2% of participants (718 people) who received the placebo (with no active ingredient)

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Visible changessuch as cloudiness, discoloration, or particles in the solutionindicate degradation and mean the medication is unsafe to inject

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Pharmacies must: Cease production of compounded semaglutide that duplicates FDA-approved products Dispense compounded medications only when supported by a valid, patient-specific prescription that meets Section 503A criteria Remaining Legal Pathways for Compounded Semaglutide Compounded semaglutide may be prescribed only in rare cases where an FDA-approved product cannot be used, such as a documented allergy to an inactive ingredient