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In clinical trial protocols, retatrutide followed a structured dose-escalation schedule designed to minimise gastrointestinal side effects the most commonly reported adverse effects with this class of medication

At meetings scheduled for July 23 and 24 at the FDA's White Oak Campus in Silver Spring, Maryland, the FDA's Pharmacy Compounding Advisory Committee will consider whether to recommend adding seven peptide substances to the agency's 503A Bulks List, which would allow them to be used in certain compounded prescription drugs

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