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Safety

Melanotan II

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

Total reports
8
Reports flagged serious
8

“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. Renal Artery Thrombosis5 reports
  2. Renal Infarct3 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.