Safety

Ipamorelin

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

Total reports
11
Reports flagged serious
4

“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. Recalled Product Administered4 reports
  2. Rash2 reports
  3. Abdominal Pain Upper1 reports
  4. Acute Kidney Injury1 reports
  5. Arthralgia1 reports
  6. Blood Glucose Increased1 reports
  7. Blood Hiv Rna Increased1 reports
  8. Blood Potassium Decreased1 reports
  9. Blood Pressure Increased1 reports
  10. Chills1 reports
  11. Constipation1 reports
  12. Dehydration1 reports
  13. Drug Dose Omission By Device1 reports
  14. Drug Hypersensitivity1 reports
  15. Dysphagia1 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.