Safety
Dulaglutide
Adverse-event report summary for Dulaglutide, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 2,300
- Reports flagged serious
- 1,885
“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
- Nausea220 reports
- Vomiting167 reports
- Diarrhoea160 reports
- Acute Kidney Injury147 reports
- Drug Interaction124 reports
- Dyspnoea116 reports
- Blood Glucose Increased94 reports
- Hyperglycaemia94 reports
- Metabolic Acidosis91 reports
- Fatigue85 reports
- Drug Ineffective84 reports
- Diabetic Ketoacidosis81 reports
- Weight Decreased80 reports
- Lactic Acidosis74 reports
- Decreased Appetite73 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.