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an antipsychotic agent of the butyrophenone group; used for the management of symptoms of psychoses and for control of the vocal utterances and tics of gilles de la tourette's syndrome.
Miller-Keane Encyclopedia and Dictionary of Medicine, Nursing, and Allied Health, Seventh Edition. © 2003 by Saunders, an imprint of Elsevier, Inc. All rights reserved.


Apo-Haloperidol (CA), Dozic (UK), Novo-Peridol (CA), Peridol (CA), PMS Haloperidol (CA), Serenace (UK)

haloperidol decanoate

Haldol Decanoate 50, Haloperidol LA Omega (CA)

haloperidol lactate


Pharmacologic class: Butyrophenone

Therapeutic class: Antipsychotic

Pregnancy risk category C

FDA Box Warning

• Drug increased mortality in elderly patients with dementia-related psychosis. Although causes of death were varied, most appeared to be cardiovascular or infectious. Drug isn't approved for treatment of dementia-related psychosis.


Unknown. Thought to block postsynaptic dopamine receptors in brain and increase dopamine turnover rate, inhibiting signs and symptoms of psychosis.


Injection (decanoate): 50 mg/ml, 100 mg/ml

Injection (lactate): 5 mg/ml

Oral concentrate (lactate): 2 mg/ml

Tablets: 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg

Indications and dosages

Symptomatic treatment of psychotic disorders or Tourette syndrome

Adults: For moderate symptoms, 0.5 to 2 mg P.O. two to three times daily. For severe symptoms or chronic or resistant disorder, 3 to 5 mg P.O. two to three times daily, to a maximum of 100 mg daily if needed. Adjust subsequent dosages carefully based on response and tolerance. Alternatively, 2 to 5 mg I.M. (lactate) may be given for prompt control of acutely agitated patient with moderate to severe symptoms; based on response, subsequent doses may be given q hour.

Schizophrenia in patients who need prolonged parenteral antipsychotic therapy

Adults: For patient previously stabilized on oral haloperidol, initial I.M. dose (decanoate) is 10 to 20 times the previous daily P.O. haloperidol equivalent, depending on patient's stability on low or high P.O. dosage. Initially, I.M. dosage shouldn't exceed 100 mg. If conversion requires dosage above 100 mg, give balance in 3 to 7 days. Maintenance dosage is 10 to 15 times the previous daily P.O. dosage, depending on response.

Psychotic disorders

Children ages 3 to 12 or weighing 15 to 40 kg (33 to 88 lb): 0.05 to 0.15 mg/kg/day P.O. in two or three divided doses. May be increased by 0.5 mg daily given in two or three divided doses at 5- to 7-day intervals, depending on response and tolerance.

Nonpsychotic behavior disorder; Tourette syndrome; hyperactivity

Children ages 3 to 12 or weighing 15 to 40 kg (33 to 88 lb): 0.05 to 0.075 mg/kg/day P.O. in two or three divided doses

Dosage adjustment

• Elderly or debilitated patients

Off-label uses

• Nausea and vomiting

• Infantile autism

• Intractable hiccups


• Hypersensitivity to drug, tartrazine, sesame oil, or benzyl alcohol (with some products)

• Severe CNS depression or comatose states

• Parkinson's disease


Use cautiously in:

• torsades de pointes, QT interval prolongation

• patients with allergies

• hepatic disease, bone marrow depression, cardiac disease, respiratory insufficiency, CNS tumors

• history of seizures, patients receiving anticonvulsants, EEG abnormalities

• concurrent anticoagulant use

• elderly patients

• pregnant or breastfeeding patients

• children (parenteral form not recommended).


• Be aware that torsades de pointes and QT interval prolongation have occurred in patients receiving haloperidol, especially when drug is given I.V. or in doses higher than recommended. Haloperidol isn't approved for I.V. use.

Don't give decanoate form I.V.

• Administer decanoate form by deep I.M. injection using 21G needle. Two injections may be necessary; maximum volume shouldn't exceed 3 ml.

• Know that recommended interval between I.M. injections is 4 weeks.

• Dilute oral concentrate in water, soda, or juice (orange, apple, tomato) immediately before administering.

• Be aware that patient should be switched from parenteral form to oral form as soon as possible.

• Know that parenteral form is not recommended in children.

Adverse reactions

CNS: confusion, drowsiness, restlessness, extrapyramidal reactions, sedation, lethargy, insomnia, vertigo, tardive dyskinesia, seizures, neuroleptic malignant syndrome

CV: hypotension, hypertension, tachycardia, ECG changes, torsades de pointes (with I.V. use)

EENT: blurred vision, dry eyes

GI: constipation, ileus, dry mouth, anorexia

GU: urinary retention, menstrual irregularities, gynecomastia, priapism

Hematologic: anemia, leukocytosis, leukopenia

Hepatic: jaundice, drug-induced hepatitis

Metabolic: galactorrhea

Respiratory: dyspnea, respiratory depression, bronchospasm, laryngospasm

Skin: diaphoresis, photosensitivity, rash

Other: hyperpyrexia, hypersensitivity reactions


Drug-drug. Antidepressants, antihistamines, atropine, disopyramide, phenothiazines, quinidine, other anticholinergics: additive anticholinergic effects

Antihypertensives, nitrates: additive hypotension

CNS depressants (including antihistamines, opioid analgesics, sedative-hypnotics): additive CNS depression

Epinephrine: severe hypotension and tachycardia

Levodopa, pergolide: decreased therapeutic effects of haloperidol

Lithium: acute encephalopathic syndrome

Methyldopa: dementia

Rifampin: decreased haloperidol plasma level

Drug-diagnostic tests. Alanine aminotransferase, aspartate aminotransferase, thyroid function tests: increased values

Arterial blood gases, bicarbonate: altered values

White blood cells: increased or decreased count

Drug-herbs. Angel's trumpet, jimsonweed, scopolia: antagonism of cholinergic effects

Chamomile, hops, kava, skullcap, valerian: increased CNS depression

Nutmeg: reduced haloperidol efficacy

Drug-behaviors. Acute alcohol ingestion: additive hypotension

Patient monitoring

Monitor CNS status closely, especially for seizures and neuroleptic malignant syndrome (shown by extrapyramidal symptoms, hyperthermia, and autonomic disturbances).

Monitor cardiovascular status, particularly for ECG changes, blood pressure changes, torsades de pointes, and atypical rapid ventricular tachycardia, which may progress to ventricular fibrillation (with I.V. use).

• Assess respiratory status.

• Monitor liver function test results and CBC with white cell differential.

• With prolonged use, assess for tardive dyskinesia (which may occur months or even years after starting drug).

Patient teaching

• Tell patient to dilute oral concentrate with water, cola, or juice immediately before taking.

Instruct patient to immediately report signs or symptoms of serious adverse reactions, such as unusual weakness, yellowing of skin or eyes, difficulty breathing, or symptoms of neuroleptic malignant syndrome (such as fever, muscle pain or rigidity, rapid or irregular pulse, increased sweating, change in urination pattern, or decreased mental acuity).

• Advise patient to minimize GI upset by eating frequent, small servings of food and drinking adequate fluids.

• As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs, tests, herbs, and behaviors mentioned above.

McGraw-Hill Nurse's Drug Handbook, 7th Ed. Copyright © 2013 by The McGraw-Hill Companies, Inc. All rights reserved


(hăl′ō-pĕr′ĭ-dôl′, -dŏl′, -dōl′)
An antipsychotic drug, C21H23ClFNO2, often administered in its decanoate form, used in the treatment of schizophrenia and in the management of Tourette syndrome.
The American Heritage® Medical Dictionary Copyright © 2007, 2004 by Houghton Mifflin Company. Published by Houghton Mifflin Company. All rights reserved.


Haldol® Psychiatry A dopamine-blocking antipsychotic for treatment-refractory schizophrenia; it ↓ hallucinations, delusions, thought disturbances, ameliorates withdrawal and apathy, used to control Sx, and to prevent relapse; it may be used for Tourette syndrome Adverse effects Sedation, weight gain, extrapyramidal signs–which may be may be immediate–eg, parkinsonism, akathisia and acute dystonia, or late with long-term therapy–eg, tardive dyskinesia, 'rabbit' syndrome, orthostatic hypotension, cardiovascular, GI effects, potentially fatal neuroleptic malignant syndrome. See Neuroleptic malignant syndrome, Positive & Negative Symptom Scale, 'Rabbit syndrome, ' Schizophrenia. Cf Clozapine.
McGraw-Hill Concise Dictionary of Modern Medicine. © 2002 by The McGraw-Hill Companies, Inc.


A butyrophenone drug used in the treatment of psychiatric disorders. It is similar in its effects to the PHENOTHIAZINE derivative drugs. The drug is on the WHO official list. Brand names are Dozic, Haldol, Haloperidol and Serenace.
Collins Dictionary of Medicine © Robert M. Youngson 2004, 2005
References in periodicals archive ?
The researchers found that for haloperidol and second-generation antipsychotics versus placebo, there was no difference in sedation status, delirium duration, hospital length of stay, or mortality.
* Haloperidol was started at 2.5 mg (age <70) or 1.25 mg (age [greater than or equal to]70) every 12 hours and titrated to a maximum dose of 20 mg/d as tolerated.
Patients in the KH group were given 0.04 mg/kg haloperidol plus 0.5 mg/kg ketamine IV in a 5 mL syringe, and patients in the PH group were given 0.04 mg/kg haloperidol plus 0.5 mg/kg pethidine IV in a 5 mL syringe.
As the haloperidol was used to induce the catalepsy, therefore, there was no standard to compare with the test drugs.
An hour after the last administrations of drug or saline administration, MK-801, apomorphine hydrochloride hemihydrate, or haloperidol were injected to mice, and then the animals were subjected to appropriate schizophrenia model.
Olanzapine was supplied by Eli Lilly Research Laboratories (Indianapolis, IN, USA), and haloperidol was purchased from Sigma (St.
Haloperidol, chlorpromazine, MG-132, pyrrolidine dithiocarbamate (PDTC), aprotinin, phenylmethylsulfonyl fluoride (PMSF), [beta]-mercaptoethanol, brilliant blue G-colloidal concentrate, Brij 35 solution, diethyl pyrocarbonate (DEPC), dithiothreitol (DTT), N-(2-hydroxyethyl)piperazine-N -(2-ethanesulfonic acid) (HEPES), leupeptin, lipopolysaccharide (LPS; Escherichia coli, serotype 0127: B8), parthenolide, and 3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide (MTT) were purchased from Sigma-Aldrich (St.
Haloperidol for treatment of cannabinoid hyperemesis syndrome, The American Journal of Emergency Medicine, 31, 1003.e5-1003e6.
[3] Many antipsychotics (both typical and atypical) like chlorpromazine, fluphenazine, haloperidol, trifluoperazine, amisulpride, olanzapine and risperidone have been implicated.
Side effects profile of haloperidol and granisetron like headache, constipation, dizziness, extrapyramidal symptoms were observed and noted.
As observacoes comportamentais dos Grupos 1 (haloperidol) e 2 (EA) aconteceram em tres etapas distintas, conforme delineamento ABA, no qual a letra "A" representa observacoes na ausencia do tratamento (haloperidol ou EA) e "B" observacoes na presenca dos tratamentos (YOUNG, 2003).
Antipsychotics such as haloperidol and risperidone are associated with a significant and dose-related increase in mortality in elderly patients with dementia, compared with antidepressants or nonuse, a retrospective case-control study involving 90,786 patients has found.