Does HALOPERIDOL Cause Product administration error? 44 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 44 reports of Product administration error have been filed in association with HALOPERIDOL (Haloperidol). This represents 0.3% of all adverse event reports for HALOPERIDOL.
44
Reports of Product administration error with HALOPERIDOL
0.3%
of all HALOPERIDOL reports
4
Deaths
22
Hospitalizations
How Dangerous Is Product administration error From HALOPERIDOL?
Of the 44 reports, 4 (9.1%) resulted in death, 22 (50.0%) required hospitalization, and 2 (4.5%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HALOPERIDOL. However, 44 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which HALOPERIDOL Alternatives Have Lower Product administration error Risk?
HALOPERIDOL vs HALOPERIDOL DECANOATE
HALOPERIDOL vs HECTOROL
HALOPERIDOL vs HEMIN
HALOPERIDOL vs HEPARIN
HALOPERIDOL vs HEPARIN\SODIUM