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The safety profile was consistent with GLP-1 receptor agonists, primarily featuring transient, mild-to-moderate gastrointestinal adverse events (e.g., nausea, 55%), with low discontinuation rates (6-8.4%)

Lee TC, Ivester P, Hester AG, Sergeant S, Case LD, Morgan T,

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Retatrutide, in clinical trials, is administered via subcutaneous injection, typically once weekly, with doses ranging from 0.5 mg to 12 mg

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