Safety

Semaglutide

Adverse-event report summary for Semaglutide, drawn from the FDA Adverse Event Reporting System (FAERS).

Total reports
7,580
Reports flagged serious
5,734

“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

  1. Nausea1,075 reports
  2. Vomiting940 reports
  3. Diarrhoea646 reports
  4. Off Label Use485 reports
  5. Drug Ineffective463 reports
  6. Fatigue457 reports
  7. Weight Decreased425 reports
  8. Dyspnoea401 reports
  9. Dizziness359 reports
  10. Weight Increased353 reports
  11. Acute Kidney Injury346 reports
  12. Headache346 reports
  13. Drug Interaction308 reports
  14. Constipation301 reports
  15. Malaise297 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.