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At least two of those cases were associated with deaths.
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In February 2026, the FDA publicly announced its intent to take action targeting mass-marketed, non-FDA-approved compounded GLP1 products, emphasizing that promotional claims implying equivalence to FDAapproved drugs can trigger enforcement risk
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Retatrutide 24mg a large-format supply of the triple incretin receptor agonist (GIP/GLP-1/Glucagon) designed for extended research programs
