Safety

Teduglutide

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

Total reports
9,301
Reports flagged serious
8,778

“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 Infection1,120 reports
  2. Weight Decreased1,062 reports
  3. Product Dose Omission Issue1,037 reports
  4. Diarrhoea848 reports
  5. Abdominal Pain743 reports
  6. Nausea732 reports
  7. Weight Increased683 reports
  8. Dehydration664 reports
  9. Vomiting627 reports
  10. Death595 reports
  11. Abdominal Distension552 reports
  12. Pyrexia504 reports
  13. Inappropriate Schedule Of Product Administration471 reports
  14. Product Use Issue467 reports
  15. Decreased Appetite464 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.