Safety
Ipamorelin
Adverse-event report summary for Ipamorelin, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 10
- Reports flagged serious
- 3
“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
- Recalled Product Administered4 reports
- Rash2 reports
- Arthralgia1 reports
- Blood Hiv Rna Increased1 reports
- Blood Pressure Increased1 reports
- Chills1 reports
- Constipation1 reports
- Dehydration1 reports
- Drug Dose Omission By Device1 reports
- Drug Hypersensitivity1 reports
- Euphoric Mood1 reports
- Feeling Jittery1 reports
- Hypokalaemia1 reports
- Injection Related Reaction1 reports
- Injection Site Abscess1 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.