Safety

Teduglutide

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

Total reports
9,130
Reports flagged serious
8,618

“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. Vascular Device Infection1,094 reports
  2. Weight Decreased1,038 reports
  3. Product Dose Omission Issue1,011 reports
  4. Diarrhoea820 reports
  5. Abdominal Pain724 reports
  6. Nausea712 reports
  7. Weight Increased665 reports
  8. Dehydration657 reports
  9. Vomiting612 reports
  10. Death588 reports
  11. Abdominal Distension537 reports
  12. Pyrexia488 reports
  13. Inappropriate Schedule Of Product Administration464 reports
  14. Product Use Issue456 reports
  15. Decreased Appetite452 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.