Does DESMOPRESSIN Cause Product administration error? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Product administration error have been filed in association with DESMOPRESSIN (Desmopressin Acetate). This represents 0.7% of all adverse event reports for DESMOPRESSIN.
29
Reports of Product administration error with DESMOPRESSIN
0.7%
of all DESMOPRESSIN reports
0
Deaths
12
Hospitalizations
How Dangerous Is Product administration error From DESMOPRESSIN?
Of the 29 reports, 12 (41.4%) required hospitalization, and 2 (6.9%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DESMOPRESSIN. However, 29 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which DESMOPRESSIN Alternatives Have Lower Product administration error Risk?
DESMOPRESSIN vs DESOGESTREL
DESMOPRESSIN vs DESOGESTREL\ETHINYL ESTRADIOL
DESMOPRESSIN vs DESONIDE
DESMOPRESSIN vs DESOXIMETASONE
DESMOPRESSIN vs DESVENLAFAXINE