Safety
Sermorelin
Adverse-event report summary for Sermorelin, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 58
- Reports flagged serious
- 35
“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
- Pruritus6 reports
- Nausea5 reports
- Hypersensitivity4 reports
- Malaise4 reports
- Rash4 reports
- Anaphylactic Reaction3 reports
- Burning Sensation3 reports
- Erythema3 reports
- Hyperhidrosis3 reports
- Infection3 reports
- Injection Site Pruritus3 reports
- Injection Site Urticaria3 reports
- Pain3 reports
- Swelling3 reports
- Wrong Product Administered3 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.