Does HALOPERIDOL Cause Wrong product administered? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Wrong product administered have been filed in association with HALOPERIDOL (Haloperidol). This represents 0.2% of all adverse event reports for HALOPERIDOL.
29
Reports of Wrong product administered with HALOPERIDOL
0.2%
of all HALOPERIDOL reports
8
Deaths
8
Hospitalizations
How Dangerous Is Wrong product administered From HALOPERIDOL?
Of the 29 reports, 8 (27.6%) resulted in death, 8 (27.6%) required hospitalization, and 1 (3.4%) were considered life-threatening.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HALOPERIDOL. However, 29 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which HALOPERIDOL Alternatives Have Lower Wrong product administered Risk?
HALOPERIDOL vs HALOPERIDOL DECANOATE
HALOPERIDOL vs HECTOROL
HALOPERIDOL vs HEMIN
HALOPERIDOL vs HEPARIN
HALOPERIDOL vs HEPARIN\SODIUM