Safety
Lixisenatide
Adverse-event report summary for Lixisenatide, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 334
- Reports flagged serious
- 303
“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
- Blood Glucose Increased40 reports
- Nausea32 reports
- Hypoglycaemia28 reports
- Diarrhoea25 reports
- Vomiting24 reports
- Malaise23 reports
- Weight Decreased19 reports
- Diabetic Ketoacidosis18 reports
- Off Label Use15 reports
- Abdominal Discomfort14 reports
- Hyperglycaemia13 reports
- Asthenia12 reports
- Decreased Appetite12 reports
- Abdominal Distension11 reports
- Dizziness11 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.