Does VALPROATE Cause Wrong patient received product? 102 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 102 reports of Wrong patient received product have been filed in association with VALPROATE (Valproate Sodium). This represents 0.6% of all adverse event reports for VALPROATE.
102
Reports of Wrong patient received product with VALPROATE
0.6%
of all VALPROATE reports
21
Deaths
43
Hospitalizations
How Dangerous Is Wrong patient received product From VALPROATE?
Of the 102 reports, 21 (20.6%) resulted in death, 43 (42.2%) required hospitalization, and 18 (17.6%) were considered life-threatening.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VALPROATE. However, 102 reports have been filed with the FAERS database.
What Other Side Effects Does VALPROATE Cause?
Foetal exposure during pregnancy (1,982)
Drug ineffective (1,268)
Seizure (1,083)
Epilepsy (878)
Somnolence (843)
Off label use (744)
Drug abuse (705)
Sopor (577)
Dysmorphism (552)
Drug interaction (513)
What Other Drugs Cause Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which VALPROATE Alternatives Have Lower Wrong patient received product Risk?
VALPROATE vs VALPROIC ACID
VALPROATE vs VALPROMIDE
VALPROATE vs VALSARTAN
VALPROATE vs VALTREX
VALPROATE vs VAMOROLONE