Does VALPROATE Cause Condition aggravated? 372 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 372 reports of Condition aggravated have been filed in association with VALPROATE (Valproate Sodium). This represents 2.3% of all adverse event reports for VALPROATE.
372
Reports of Condition aggravated with VALPROATE
2.3%
of all VALPROATE reports
18
Deaths
174
Hospitalizations
How Dangerous Is Condition aggravated From VALPROATE?
Of the 372 reports, 18 (4.8%) resulted in death, 174 (46.8%) required hospitalization, and 40 (10.8%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VALPROATE. However, 372 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which VALPROATE Alternatives Have Lower Condition aggravated Risk?
VALPROATE vs VALPROIC ACID
VALPROATE vs VALPROMIDE
VALPROATE vs VALSARTAN
VALPROATE vs VALTREX
VALPROATE vs VAMOROLONE