Safety
Pramlintide
Adverse-event report summary for Pramlintide, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 84
- Reports flagged serious
- 42
“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 Increased20 reports
- Nausea15 reports
- Fatigue11 reports
- Dyspnoea9 reports
- Blood Glucose Decreased8 reports
- Diarrhoea8 reports
- Chest Pain7 reports
- Hypertension7 reports
- Weight Increased7 reports
- Dizziness6 reports
- Weight Decreased6 reports
- Decreased Appetite5 reports
- Drug Ineffective5 reports
- Gait Disturbance5 reports
- Oedema Peripheral5 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.