Safety
Retatrutide
Adverse-event report summary for Retatrutide, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 27
- Reports flagged serious
- 22
“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
- Vomiting5 reports
- Nausea4 reports
- Fatigue3 reports
- Abdominal Pain2 reports
- Burning Sensation2 reports
- Dehydration2 reports
- Headache2 reports
- Heart Rate Increased2 reports
- Illness2 reports
- Intentional Product Misuse2 reports
- Metabolic Acidosis2 reports
- Neuropathy Peripheral2 reports
- Off Label Use2 reports
- Product Advertising Issue2 reports
- Product Use In Unapproved Indication2 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.