Safety
CJC-1295
Adverse-event report summary for CJC-1295, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 2
- Reports flagged serious
- 2
“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
- Drug Hypersensitivity1 reports
- Injection Site Abscess1 reports
- Product Dispensing Error1 reports
- Product Preparation Error1 reports
- Recalled Product Administered1 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.