Safety
Desmopressin
Adverse-event report summary for Desmopressin, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 6,709
- Reports flagged serious
- 5,059
“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
- Hyponatraemia701 reports
- Drug Ineffective524 reports
- Off Label Use407 reports
- Headache319 reports
- Nausea263 reports
- Vomiting253 reports
- Fatigue243 reports
- Drug Interaction209 reports
- Fall197 reports
- Dizziness192 reports
- Diarrhoea186 reports
- Product Use In Unapproved Indication184 reports
- Malaise180 reports
- Asthenia168 reports
- Seizure164 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.