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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 Hyperprolactinaemia? 37 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 37 reports of Hyperprolactinaemia have been filed in association with VALPROATE (Valproate Sodium). This represents 0.2% of all adverse event reports for VALPROATE.

37
Reports of Hyperprolactinaemia with VALPROATE
0.2%
of all VALPROATE reports
0
Deaths
13
Hospitalizations

How Dangerous Is Hyperprolactinaemia From VALPROATE?

Of the 37 reports, 13 (35.1%) required hospitalization.

Is Hyperprolactinaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for VALPROATE. However, 37 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 Hyperprolactinaemia?

RISPERIDONE (4,124) PALIPERIDONE (1,427) OLANZAPINE (520) ARIPIPRAZOLE (459) QUETIAPINE (331) HALOPERIDOL (214) CLOZAPINE (157) AMISULPRIDE (135) SERTRALINE (120) LITHIUM (76)

Which VALPROATE Alternatives Have Lower Hyperprolactinaemia Risk?

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

Related Pages

VALPROATE Full Profile All Hyperprolactinaemia Reports All Drugs Causing Hyperprolactinaemia VALPROATE Demographics