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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 RISPERIDONE Cause Hyperprolactinaemia? 4,124 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 4,124 reports of Hyperprolactinaemia have been filed in association with RISPERIDONE (Risperidone). This represents 5.2% of all adverse event reports for RISPERIDONE.

4,124
Reports of Hyperprolactinaemia with RISPERIDONE
5.2%
of all RISPERIDONE reports
22
Deaths
257
Hospitalizations

How Dangerous Is Hyperprolactinaemia From RISPERIDONE?

Of the 4,124 reports, 22 (0.5%) resulted in death, 257 (6.2%) required hospitalization, and 7 (0.2%) were considered life-threatening.

Is Hyperprolactinaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RISPERIDONE. However, 4,124 reports have been filed with the FAERS database.

What Other Side Effects Does RISPERIDONE Cause?

Gynaecomastia (24,453) Off label use (10,376) Abnormal weight gain (9,418) Weight increased (6,885) Emotional disorder (5,809) Product use in unapproved indication (5,551) Drug ineffective (5,232) Injury (4,447) Galactorrhoea (3,513) Emotional distress (3,195)

What Other Drugs Cause Hyperprolactinaemia?

PALIPERIDONE (1,427) OLANZAPINE (520) ARIPIPRAZOLE (459) QUETIAPINE (331) HALOPERIDOL (214) CLOZAPINE (157) AMISULPRIDE (135) SERTRALINE (120) LITHIUM (76) VENLAFAXINE (71)

Which RISPERIDONE Alternatives Have Lower Hyperprolactinaemia Risk?

RISPERIDONE vs RITALIN RISPERIDONE vs RITLECITINIB RISPERIDONE vs RITODRINE RISPERIDONE vs RITONAVIR RISPERIDONE vs RITUXAN

Related Pages

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