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Description

Retatrutide is an investigational research compound and is not FDA approved

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NIDDK P30 DK04056, UE5 DK137285, and U24 DK132733

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Retatrutide is not approved by the MHRA or EMA and is not available as a licensed prescription medicine in the UK

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95% of gastrointestinal (GI) related adverse events were reported as mild or moderate

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Weeks 25-48: Optimization and Maintenance The latter half of the first year sees continued glucose improvements for most users, though the rate of change typically slows compared to earlier months

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That is a risk the clinical trials do not measure

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