Does RISPERIDONE Cause Product use in unapproved indication? 5,551 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5,551 reports of Product use in unapproved indication have been filed in association with RISPERIDONE (Risperidone). This represents 7.0% of all adverse event reports for RISPERIDONE.
5,551
Reports of Product use in unapproved indication with RISPERIDONE
7.0%
of all RISPERIDONE reports
69
Deaths
686
Hospitalizations
How Dangerous Is Product use in unapproved indication From RISPERIDONE?
Of the 5,551 reports, 69 (1.2%) resulted in death, 686 (12.4%) required hospitalization, and 83 (1.5%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RISPERIDONE. However, 5,551 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)
Drug ineffective (5,232)
Injury (4,447)
Hyperprolactinaemia (4,124)
Galactorrhoea (3,513)
Emotional distress (3,195)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
TACROLIMUS (5,057)
CYCLOSPORINE (5,019)
Which RISPERIDONE Alternatives Have Lower Product use in unapproved indication Risk?
RISPERIDONE vs RITALIN
RISPERIDONE vs RITLECITINIB
RISPERIDONE vs RITODRINE
RISPERIDONE vs RITONAVIR
RISPERIDONE vs RITUXAN