Safety
Semaglutide
Adverse-event report summary for Semaglutide, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 6,618
- Reports flagged serious
- 5,186
“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
- Nausea943 reports
- Vomiting835 reports
- Diarrhoea589 reports
- Off Label Use426 reports
- Fatigue396 reports
- Dyspnoea382 reports
- Weight Decreased379 reports
- Drug Ineffective374 reports
- Dizziness328 reports
- Headache305 reports
- Malaise278 reports
- Acute Kidney Injury268 reports
- Abdominal Pain262 reports
- Constipation249 reports
- Weight Increased245 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.