Safety
Desmopressin
Adverse-event report summary for Desmopressin, drawn from the FDA Adverse Event Reporting System (FAERS).
- Total reports
- 6,588
- Reports flagged serious
- 4,965
“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
- Hyponatraemia691 reports
- Drug Ineffective515 reports
- Off Label Use394 reports
- Headache315 reports
- Nausea251 reports
- Vomiting249 reports
- Fatigue238 reports
- Drug Interaction192 reports
- Fall191 reports
- Dizziness186 reports
- Product Use In Unapproved Indication182 reports
- Diarrhoea181 reports
- Malaise177 reports
- Asthenia165 reports
- Seizure163 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.