Safety
Dulaglutide
Adverse-event report summary for Dulaglutide, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 2,394
- Reports flagged serious
- 1,967
“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
- Nausea226 reports
- Vomiting172 reports
- Diarrhoea167 reports
- Acute Kidney Injury160 reports
- Drug Interaction136 reports
- Dyspnoea118 reports
- Blood Glucose Increased103 reports
- Metabolic Acidosis98 reports
- Hyperglycaemia95 reports
- Lactic Acidosis87 reports
- Drug Ineffective86 reports
- Fatigue86 reports
- Diabetic Ketoacidosis82 reports
- Weight Decreased82 reports
- Hypotension75 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.