Safety

BPC-157

Adverse-event report summary for BPC-157, drawn from the FDA Adverse Event Reporting System (FAERS).

Total reports
18
Reports flagged serious
16

“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. Drug Ineffective3 reports
  2. Erythema3 reports
  3. Abdominal Discomfort2 reports
  4. Balance Disorder2 reports
  5. Drug Intolerance2 reports
  6. Dyspnoea2 reports
  7. Flushing2 reports
  8. Headache2 reports
  9. Hypersensitivity2 reports
  10. Nausea2 reports
  11. Product Label Issue2 reports
  12. Product Use In Unapproved Indication2 reports
  13. Abdominal Pain1 reports
  14. Abdominal Pain Upper1 reports
  15. Adverse Drug Reaction1 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.