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Red Flags When Evaluating a Peptide Vendor The FDA's 2025 and 2026 enforcement actions targeted suppliers whose labeling or website language implied human use, suggested therapeutic effects, or marketed the compound by comparison to FDA-approved drugs

They warn that the lack of rigorous clinical trials and standardized protocols raise serious safety concerns, including the risk of hepatotoxicity (liver damage caused by chemicals) and allergic reactions like anaphylaxis

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Although subcutaneous semaglutide is already approved by the FDA for cardiovascular risk reduction in adults with type 2 diabetes and established atherosclerotic cardiovascular disease, oral semaglutide is currently approved only for glycaemic control