Safety
Retatrutide
Adverse-event report summary for Retatrutide, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 44
- Reports flagged serious
- 33
“Serious” is FAERS’s own report-level flag (e.g. death, hospitalization, or another outcome the reporter marked as serious) and does not indicate a verified or compound-caused outcome.
Most frequently reported reactions
- Vomiting8 reports
- Nausea7 reports
- Fatigue4 reports
- Heart Rate Increased4 reports
- Illness4 reports
- Product Use In Unapproved Indication4 reports
- Abdominal Pain3 reports
- Burning Sensation3 reports
- Feeling Abnormal3 reports
- Product Advertising Issue3 reports
- Product Use Issue3 reports
- Acute Kidney Injury2 reports
- Blood Potassium Decreased2 reports
- Dehydration2 reports
- Dysphagia2 reports
Counts reflect the most-reported reaction terms (MedDRA preferred terms) associated with reports naming this compound. A single report can list multiple reactions, so reaction counts need not sum to the total number of reports.