Safety
Tirzepatide
Adverse-event report summary for Tirzepatide, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 3,153
- Reports flagged serious
- 1,859
“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
- Nausea385 reports
- Vomiting342 reports
- Diarrhoea268 reports
- Fatigue157 reports
- Constipation143 reports
- Off Label Use143 reports
- Drug Interaction142 reports
- Drug Ineffective110 reports
- Headache106 reports
- Dizziness105 reports
- Decreased Appetite103 reports
- Acute Kidney Injury101 reports
- Weight Decreased97 reports
- Abdominal Pain94 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.