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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 Wrong product administered? 21 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Wrong product administered have been filed in association with VALPROATE (Valproate Sodium). This represents 0.1% of all adverse event reports for VALPROATE.

21
Reports of Wrong product administered with VALPROATE
0.1%
of all VALPROATE reports
0
Deaths
9
Hospitalizations

How Dangerous Is Wrong product administered From VALPROATE?

Of the 21 reports, 9 (42.9%) required hospitalization.

Is Wrong product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for VALPROATE. However, 21 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 product administered?

INSULIN LISPRO (337) INSULIN GLARGINE (226) RISPERIDONE (141) QUETIAPINE (137) ACETAMINOPHEN (133) INSULIN ASPART (112) CLOZAPINE (106) INSULIN HUMAN (104) TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104) IBUPROFEN (102)

Which VALPROATE Alternatives Have Lower Wrong product administered Risk?

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

Related Pages

VALPROATE Full Profile All Wrong product administered Reports All Drugs Causing Wrong product administered VALPROATE Demographics