Retatrutide risks and side effects: what the clinical trials actually show

Retatrutide is an investigational once-weekly injectable that activates the GIP, GLP-1 and glucagon receptors. In the published phase 2 obesity trial, the most common side effects were gastrointestinal (nausea, diarrhea, vomiting, constipation), they were dose-related and mostly mild to moderate, and heart rate rose in a dose-dependent way, peaking at 24 weeks. As of September 2026 retatrutide is not approved by the FDA or the EMA; Eli Lilly has said it plans to file for U.S. approval in the first quarter of 2027.

Method in one line: every figure on this site comes from a peer-reviewed publication, a ClinicalTrials.gov registration, an FDA prescribing document or a dated company announcement, each cited with a clickable DOI or URL on the same page.

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An independent editorial project that reads the primary literature on retatrutide and writes it up in plain language, with a preference for stating what is not known. Read the about page and the editorial policy.