Does DESMOPRESSIN Cause Product dose omission in error? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product dose omission in error have been filed in association with DESMOPRESSIN (Desmopressin Acetate). This represents 0.2% of all adverse event reports for DESMOPRESSIN.
9
Reports of Product dose omission in error with DESMOPRESSIN
0.2%
of all DESMOPRESSIN reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission in error From DESMOPRESSIN?
Of the 9 reports, 3 (33.3%) required hospitalization, and 3 (33.3%) were considered life-threatening.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DESMOPRESSIN. However, 9 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 dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which DESMOPRESSIN Alternatives Have Lower Product dose omission in error Risk?
DESMOPRESSIN vs DESOGESTREL
DESMOPRESSIN vs DESOGESTREL\ETHINYL ESTRADIOL
DESMOPRESSIN vs DESONIDE
DESMOPRESSIN vs DESOXIMETASONE
DESMOPRESSIN vs DESVENLAFAXINE