Safety
Semax
Adverse-event report summary for Semax, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 2
- Reports flagged serious
- 1
“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
- Dyspnoea1 reports
- Electrocardiogram Qt Prolonged1 reports
- Eye Pain1 reports
- Product Advertising Issue1 reports
- Somnolence1 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.