Updated May 30, 2026, 4:23 PM
Antipsychotic/neuroleptic/antiemeticUS FDA Database Verified

chlorproMAZINE (Rx)

Generic: ChlorproMAZINE

Brand: not specified

(klor-proe'ma-zeen)

Pregnancy Category: C

Pharmacological Action

Depresses cerebral cortex, hypothalamus, limbic system, which control activity, aggression; blocks neurotransmission produced by dopamine at synapse; exhibits a strong a-adrenergic, anticholinergic blocking action; mechanism for antipsychotic effects is unclear

Therapeutic outcome: Decreased signs and symptoms of psychosis; control of nausea, vomiting, intractable hiccups, decreased anxiety preoperatively

Uses

Psychotic disorders, Tourette's syndrome, mania, schizophrenia, anxiety, intractable hiccups (adults), nausea, vomiting, preoperative relaxation, acute intermittent porphyria, behavioral problems in children, nonpsychotic patients with dementia

Contraindications

Hypersensitivity, circulatory collapse, liver damage, cerebral arteriosclerosis, coronary disease, severe hypo/hypertension, blood dyscrasias, coma, child <6 mo, brain damage, bone marrow depression, alcohol and barbiturate withdrawal, closed-angle glaucoma

Precautions: Pregnancy C, breastfeeding, geriatric, seizure disorders, hypertension, hepatic/cardiac disease, prostate enlargement, pulmonary/Parkinson's disease

BLACK BOX WARNING: Dementia; increased mortality in elderly patients with dementia-related psychosis

Dosage & Routes

Psychosis

Adult: PO 10-50 mg q1-4 hr initially, then increase up to 2 g/day if necessary; IM 10-50 mg q1-4 hr, usual dose 300-800 mg/day

Geriatric: PO 10-25 mg daily-bid, increased by 10-25 mg/day q4-7 day, max 800 mg/day Child >6 mo: PO 0.55 mg/kg q4-6 hr; IM 0.5 mg/kg q6-8 hr Nausea and vomiting

Adult: PO 10-25 mg q4-6 hr prn; IM 25-50 mg q3 hr prn; max 400 mg/day; IV 25-50 mg daily-qid Child ≥6 mo: PO 0.55 mg/kg q4-6 hr; IM q6-8 hr; IM <5 yr or <22.7 kg 40 mg; max IM 5-10 yr or 22.7-45.5 kg 75 mg Intractable hiccups/acute intermittent porphyria

Adult: PO 25-50 mg tid-qid; IM 25-50 mg (used only if PO dose does not work); IV 25-50 mg in 500-1000 ml saline (only for severe hiccups)

Available forms: Tabs 10, 25, 50, 100; inj 25 mg/ml

Implementation - Periodically attempt dosage reduction in patients with behavioral problems - Give with full glass of water, milk; or give with food to decrease GI upset - Store in tight, light-resistant container, oral sol in amber bottle IM route - Store in tight, light-resistant container - Use gloves to prepare product; if product touches skin, wash with soap and water to prevent contact dermatitis - Inject in deep muscle mass; do not give SUBCUT; may be diluted with 0.9% NaCl, 2% procaine as prescribed; do not administer sol with a precipitate - Remain lying down after IM inj for at least 30 min Rectal route - Give after placing in refrigerator for 30 min if too soft to insert; this route is used for nausea, vomiting, hiccups - Avoid skin contact with injection solution; may cause contact dermatitis Direct IV - Give by direct IV by diluting with 0.9% NaCl to a concentration of 1 mg/1 ml; administer at a rate of 1 mg/2 min, never give undiluted - Give by intermittent IV infusion diluting 50 mg/500-1000 ml of D5 W, D10 W, 0.9% NaCl, 0.45% NaCl, LR, Ringer's over ½ hr or combinations (used for intractable hiccups)

Adverse Effects

CNS: Neuroleptic malignant syndrome, dizziness, extrapyramidal symptoms: pseudoparkinsonism, akathisia, dystonia, tardive dyskinesia, seizures, headache

CV: Orthostatic hypotension, hypertension, cardiac arrest, ECG changes, tachycardia

EENT: Blurred vision, glaucoma, dry eyes

ENDO: SIADH

GI: Dry mouth, nausea, vomiting, anorexia, constipation, diarrhea, cholestatic jaundice, weight gain

GU: Urinary retention, enuresis, impotence, amenorrhea, gynecomastia, breast engorgement

HEMA: Anemia, leukopenia, leukocytosis, agranulocytosis

INTEG: Rash, photosensitivity, dermatitis

RESP: Laryngospasm, dyspnea, respiratory depression

SYST: Death in geriatric patients with dementia

Pharmacokinetics

Absorption: Variable (PO); well absorbed (IM)

Distribution: Widely distributed; crosses placenta

Metabolism: Liver, GI mucosa extensively

Excretion: Kidneys

Half-life: 30 hr

Pharmacodynamics

PO: Onset ½-1 hr, Peak Unknown, Duration 4-6 hr

RECT: Onset 12 hr, Peak Unknown, Duration 3-4 hr

IM: Onset Unknown, Peak Unknown, Duration 4-8 hr

IV: Onset Rapid, Peak Unknown, Duration Unknown Duration PO ext rel is 10-12 hr.

Interactions

Individual drugs

Alcohol: increased effects of both products, oversedation Aluminum hydroxide, magnesium hydroxide: decreased absorption Bromocriptine, levodopa: decreased antiparkinsonian activity

EPINEPHrine: increased toxicity

Lithium: decreased chlorproMAZINE levels Valproic acid: increased valproic acid level

Warfarin: decreased anticoagulant effect

Drug classifications

Antacids: decreased absorption Anticholinergics, antidepressants, antiparkinsonian agents: increased anticholinergic effects

Anticonvulsants: decreased seizure threshold Antidepressants, antihistamines, barbiturate anesthetics, opioids, sedative/hypnotics: increased CNS depression Antithyroid agents: increased agranulocytosis

Barbiturates: decreased serum chlorproMAZINE β-Adrenergic blockers: increased effect of both products

Drug/lab test

Increased: liver function tests

Decreased: WBC, platelets, Hgb/Hct False positive: pregnancy tests, PKU False negative: urinary steroids, 17-OHCS

Nursing Considerations

Assessment - Assess mental status: orientation, mood, behavior, presence of hallucinations, and type before initial administration and monthly; this product should significantly reduce psychotic behavior - Assess any potentially reversible cause of behavior problems in geriatric before, during therapy - Check for swallowing of PO medication; check for hoarding or giving of medication to other patients - Monitor • I&O ratio; palpate bladder if low urinary output occurs, especially in geriatric; urinalysis recommended before, during prolonged therapy - Monitor bilirubin, CBC, liver function studies, ocular exam; agranulocytosis, glaucoma, cholestatic jaundice may occur - Assess respirations q4 hr during initial treatment; establish baseline before starting treatment; report drops of 30 mm Hg; obtain baseline ECG, Q wave, and T wave changes - Check for dizziness, faintness, palpitations, tachycardia on rising; severe orthostatic hypotension is common - Identify for neuroleptic malignant syndrome: hyperpyrexia, muscle rigidity, increased CPK, altered mental status; product should be discontinued - Assess for EPS including akathisia (inability to sit still, no pattern to movements), tardive dyskinesia (bizarre movements of the jaw, mouth, tongue, extremities), pseudoparkinsonism (rigidity, tremors, pill rolling, shuffling gate); an antiparkinsonian product should be prescribed - Assess for constipation, urinary retention daily; if these occur, increase bulk, water in diet

Patient/family education - Teach patient to use good oral hygiene; frequent rinsing of mouth, sugarless gum, candy, or ice chips for dry mouth - Caution patient to avoid hazardous activities until product response is determined; dizziness, blurred vision may occur - Inform patient that orthostatic hypotension occurs often and to rise from sitting or lying position gradually, to remain lying down after IM inj for at least 30 min; tell patient to avoid hot tubs, hot showers, tub baths, since hypotension may occur; tell patient that in hot weather heat stroke may occur; take extra precautions to stay cool - Advise patient to avoid abrupt withdrawal of this product, or extrapyramidal symptoms may result; product should be withdrawn slowly - Teach patient to avoid OTC preparations (cough, hay fever, cold) unless approved by prescriber, since serious product interactions may occur; avoid use with alcohol, CNS depressants, since increased drowsiness may occur - Caution patient to use sunscreen and sunglasses to prevent burns - Teach patient about extrapyramidal symptoms and necessity of meticulous oral hygiene, since oral candidiasis may occur - Instruct patient to take antacids 2 hr before or after taking this product - Instruct patient to report sore throat, malaise, fever, bleeding, mouth sores; if these occur, CBC should be drawn and product discontinued - Teach that urine may turn pink or reddish-brown - Teach patient to use contraceptive measures

Evaluation

Positive therapeutic outcome: Decrease in emotional excitement, hallucinations, delusions, paranoia; Reorganization of patterns of thought, speech; Increase in target behaviors

Reference

Mosby's Drug Guide; Davis Drug Guide

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