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On Wednesday, the Food and Drug Administration issued a warning, calling compounded GLP-1 medications "risky for patients." "FDA is aware that some patients and health care professionals may look to unapproved versions of GLP-1 (glucagon-like peptide-1 (GLP-1) receptor agonists) drugs, including semaglutide and tirzepatide, as an option for weight loss," the FDA said

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Its unclear how many of the estimated 10 million or so Americans who use compounded versions of the medications will be affected by the changes, Lee Rosebush, the outsourcing association's chairman, said in an interview

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