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The FDA said while the medications are eligible for compounding because of shortages, the compounded versions "pose a higher risk." "Compounded drugs pose a higher risk to patient than FDA-approved drugs because compounded drugs do not undergo FDA premarket review for safety, effectiveness, or quality," the agency said in a statement

Retatrutide is the first triple hormone receptor agonist (GIP, GLP-1, glucagon) to reach Phase 3 clinical trials

adults, are considered eligible to take semaglutide, according to research published in 2024 in JAMA Cardiology

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Alluvi Retatrutide is typically intended for research and development purposes only, and appropriate laboratory protocols should always be followed