Does DESMOPRESSIN Cause Incorrect product storage? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Incorrect product storage have been filed in association with DESMOPRESSIN (Desmopressin Acetate). This represents 0.2% of all adverse event reports for DESMOPRESSIN.
7
Reports of Incorrect product storage with DESMOPRESSIN
0.2%
of all DESMOPRESSIN reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product storage From DESMOPRESSIN?
Of the 7 reports.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DESMOPRESSIN. However, 7 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 Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
Which DESMOPRESSIN Alternatives Have Lower Incorrect product storage Risk?
DESMOPRESSIN vs DESOGESTREL
DESMOPRESSIN vs DESOGESTREL\ETHINYL ESTRADIOL
DESMOPRESSIN vs DESONIDE
DESMOPRESSIN vs DESOXIMETASONE
DESMOPRESSIN vs DESVENLAFAXINE