Safety
Tirzepatide
Adverse-event report summary for Tirzepatide, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 2,641
- Reports flagged serious
- 1,463
“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
- Product Tampering408 reports
- Nausea327 reports
- Vomiting279 reports
- Diarrhoea231 reports
- Fatigue132 reports
- Constipation130 reports
- Off Label Use120 reports
- Drug Interaction104 reports
- Headache90 reports
- Drug Ineffective88 reports
- Abdominal Pain85 reports
- Incorrect Dose Administered84 reports
- Dizziness83 reports
- Abdominal Pain Upper77 reports
- Weight Decreased77 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.