Safety
Exenatide
Adverse-event report summary for Exenatide, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 4,946
- Reports flagged serious
- 1,452
“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
- Nausea1,338 reports
- Weight Decreased1,141 reports
- Blood Glucose Increased962 reports
- Decreased Appetite682 reports
- Vomiting515 reports
- Blood Glucose Decreased360 reports
- Diarrhoea330 reports
- Dizziness282 reports
- Malaise258 reports
- Incorrect Dose Administered236 reports
- Headache225 reports
- Fatigue210 reports
- Weight Increased174 reports
- Pancreatitis169 reports
- Feeling Abnormal164 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.