Does DESMOPRESSIN Cause Intentional dose omission? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Intentional dose omission have been filed in association with DESMOPRESSIN (Desmopressin Acetate). This represents 0.2% of all adverse event reports for DESMOPRESSIN.
8
Reports of Intentional dose omission with DESMOPRESSIN
0.2%
of all DESMOPRESSIN reports
0
Deaths
4
Hospitalizations
How Dangerous Is Intentional dose omission From DESMOPRESSIN?
Of the 8 reports, 4 (50.0%) required hospitalization, and 1 (12.5%) were considered life-threatening.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DESMOPRESSIN. However, 8 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 Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which DESMOPRESSIN Alternatives Have Lower Intentional dose omission Risk?
DESMOPRESSIN vs DESOGESTREL
DESMOPRESSIN vs DESOGESTREL\ETHINYL ESTRADIOL
DESMOPRESSIN vs DESONIDE
DESMOPRESSIN vs DESOXIMETASONE
DESMOPRESSIN vs DESVENLAFAXINE