Does HALOPERIDOL Cause Product use in unapproved indication? 478 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 478 reports of Product use in unapproved indication have been filed in association with HALOPERIDOL (Haloperidol). This represents 3.0% of all adverse event reports for HALOPERIDOL.
478
Reports of Product use in unapproved indication with HALOPERIDOL
3.0%
of all HALOPERIDOL reports
28
Deaths
271
Hospitalizations
How Dangerous Is Product use in unapproved indication From HALOPERIDOL?
Of the 478 reports, 28 (5.9%) resulted in death, 271 (56.7%) required hospitalization, and 44 (9.2%) 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 HALOPERIDOL. However, 478 reports have been filed with the FAERS database.
What Other Side Effects Does HALOPERIDOL Cause?
Drug ineffective (1,771)
Neuroleptic malignant syndrome (1,244)
Off label use (1,136)
Toxicity to various agents (872)
Extrapyramidal disorder (838)
Somnolence (712)
Intentional self-injury (636)
Drug interaction (596)
Weight increased (583)
Tremor (579)
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)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which HALOPERIDOL Alternatives Have Lower Product use in unapproved indication Risk?
HALOPERIDOL vs HALOPERIDOL DECANOATE
HALOPERIDOL vs HECTOROL
HALOPERIDOL vs HEMIN
HALOPERIDOL vs HEPARIN
HALOPERIDOL vs HEPARIN\SODIUM