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In recent enforcement actions, the agency identified multiple concerns with compounded GLP-1 products: use of incorrect salt forms of semaglutide that have not been studied for safety, dosing errors due to patient-drawn injections from multi-dose vials, improper storage and shipping conditions, and misleading marketing that implies FDA equivalence

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Patients referred by a licensed provider for evaluation of non-FDA-approved peptides in a structured care setting

Each person who received retatrutide started with a 2 mg dose, with amounts increasing every four weeks until they reached their targeted dose

Step 8: Label the vial with reconstitution date, concentration (mg/mL), and your calculated dose volume

2010;5(5):e10844