Does RISPERIDONE Cause Product prescribing error? 139 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 139 reports of Product prescribing error have been filed in association with RISPERIDONE (Risperidone). This represents 0.2% of all adverse event reports for RISPERIDONE.
139
Reports of Product prescribing error with RISPERIDONE
0.2%
of all RISPERIDONE reports
1
Deaths
92
Hospitalizations
How Dangerous Is Product prescribing error From RISPERIDONE?
Of the 139 reports, 1 (0.7%) resulted in death, 92 (66.2%) required hospitalization, and 23 (16.5%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RISPERIDONE. However, 139 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 Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which RISPERIDONE Alternatives Have Lower Product prescribing error Risk?
RISPERIDONE vs RITALIN
RISPERIDONE vs RITLECITINIB
RISPERIDONE vs RITODRINE
RISPERIDONE vs RITONAVIR
RISPERIDONE vs RITUXAN