Safety
Liraglutide
Adverse-event report summary for Liraglutide, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 5,486
- Reports flagged serious
- 3,386
“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
- Nausea652 reports
- Dyspnoea336 reports
- Vomiting334 reports
- Blood Glucose Increased331 reports
- Diarrhoea326 reports
- Anxiety233 reports
- Condition Aggravated226 reports
- Drug Ineffective220 reports
- Pancreatitis219 reports
- Headache216 reports
- Decreased Appetite199 reports
- Asthma191 reports
- Therapeutic Product Effect Incomplete188 reports
- Wheezing184 reports
- Hypothyroidism183 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.