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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does VALPROATE Cause Product quality issue? 31 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Product quality issue have been filed in association with VALPROATE (Valproate Sodium). This represents 0.2% of all adverse event reports for VALPROATE.

31
Reports of Product quality issue with VALPROATE
0.2%
of all VALPROATE reports
0
Deaths
9
Hospitalizations

How Dangerous Is Product quality issue From VALPROATE?

Of the 31 reports, 9 (29.0%) required hospitalization, and 2 (6.5%) were considered life-threatening.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for VALPROATE. However, 31 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 Product quality issue?

ETONOGESTREL (4,651) ALBUTEROL (4,466) TIOTROPIUM (3,821) MOMETASONE FUROATE (3,406) LIDOCAINE (3,126) FLUTICASONE\SALMETEROL (2,986) FORMOTEROL\MOMETASONE FUROATE (2,458) FENTANYL (2,450) NICOTINE (1,987) EXENATIDE (1,839)

Which VALPROATE Alternatives Have Lower Product quality issue Risk?

VALPROATE vs VALPROIC ACID VALPROATE vs VALPROMIDE VALPROATE vs VALSARTAN VALPROATE vs VALTREX VALPROATE vs VAMOROLONE

Related Pages

VALPROATE Full Profile All Product quality issue Reports All Drugs Causing Product quality issue VALPROATE Demographics