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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 Device use error? 28 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Device use error have been filed in association with RISPERIDONE (Risperidone). This represents 0.0% of all adverse event reports for RISPERIDONE.

28
Reports of Device use error with RISPERIDONE
0.0%
of all RISPERIDONE reports
4
Deaths
22
Hospitalizations

How Dangerous Is Device use error From RISPERIDONE?

Of the 28 reports, 4 (14.3%) resulted in death, 22 (78.6%) required hospitalization.

Is Device use error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RISPERIDONE. However, 28 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) Hyperprolactinaemia (4,124) Galactorrhoea (3,513)

What Other Drugs Cause Device use error?

PEGFILGRASTIM (6,001) ALBUTEROL (5,215) ALBIGLUTIDE (4,056) EVOLOCUMAB (4,002) SOMATROPIN (2,801) FLUTICASONE\SALMETEROL (1,749) FLUTICASONE (783) FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766) ERENUMAB-AOOE (711) ETANERCEPT (665)

Which RISPERIDONE Alternatives Have Lower Device use error Risk?

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

Related Pages

RISPERIDONE Full Profile All Device use error Reports All Drugs Causing Device use error RISPERIDONE Demographics