Does DESMOPRESSIN Cause Product prescribing error? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Product prescribing error have been filed in association with DESMOPRESSIN (Desmopressin Acetate). This represents 0.7% of all adverse event reports for DESMOPRESSIN.
28
Reports of Product prescribing error with DESMOPRESSIN
0.7%
of all DESMOPRESSIN reports
0
Deaths
24
Hospitalizations
How Dangerous Is Product prescribing error From DESMOPRESSIN?
Of the 28 reports, 24 (85.7%) required hospitalization, and 11 (39.3%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DESMOPRESSIN. However, 28 reports have been filed with the FAERS database.
What Other Side Effects Does DESMOPRESSIN Cause?
Hyponatraemia (686)
Drug ineffective (456)
Headache (238)
Off label use (224)
Product use in unapproved indication (164)
Nasal discomfort (163)
Product storage error (162)
Nausea (131)
Blood sodium decreased (125)
Seizure (125)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which DESMOPRESSIN Alternatives Have Lower Product prescribing error Risk?
DESMOPRESSIN vs DESOGESTREL
DESMOPRESSIN vs DESOGESTREL\ETHINYL ESTRADIOL
DESMOPRESSIN vs DESONIDE
DESMOPRESSIN vs DESOXIMETASONE
DESMOPRESSIN vs DESVENLAFAXINE