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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 issue? 140 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 140 reports of Device issue have been filed in association with RISPERIDONE (Risperidone). This represents 0.2% of all adverse event reports for RISPERIDONE.

140
Reports of Device issue with RISPERIDONE
0.2%
of all RISPERIDONE reports
1
Deaths
1
Hospitalizations

How Dangerous Is Device issue From RISPERIDONE?

Of the 140 reports, 1 (0.7%) resulted in death, 1 (0.7%) required hospitalization.

Is Device issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RISPERIDONE. However, 140 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 issue?

ADALIMUMAB (17,630) SOMATROPIN (5,131) PEGFILGRASTIM (5,071) ETANERCEPT (4,143) INSULIN GLARGINE (3,175) EXENATIDE (2,862) LEVONORGESTREL (2,623) CARBIDOPA\LEVODOPA (2,574) GOLIMUMAB (1,827) USTEKINUMAB (1,716)

Which RISPERIDONE Alternatives Have Lower Device issue Risk?

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

Related Pages

RISPERIDONE Full Profile All Device issue Reports All Drugs Causing Device issue RISPERIDONE Demographics