Pimozide is used in its oral preparation in schizophrenia and chronic psychosis (on-label indications in Europe only), Gilles de la Tourette syndrome and resistant tics (Europe, USA and Canada). In Germany the 1mg tablet is indicated for the treatment of some forms of reactive depression.
Off-label use
Pimozide has been used for ADHD (Attention Deficit Hyperactivity Disorder) in children and adolescents, when not controlled by monotherapy with a stimulant.[citation needed]
Pimozide has been used in the treatment of delusional disorder. (Munro, 1999)
Chemistry
Pimozide is a diphenylbutylpiperidine derivative.
Pharmacology
Pharmacokinetics
Plasma levels of pimozide can vary widely between patients, and in insufficient response therapeutic drug monitoring may be required to ascertain that the patient is developing adequate plasma levels before withdrawing the drug and attempting other antipsychotics.
Pharmacodynamics
Pimozide blocks the following postsynaptic receptors according to Bezchlinyk-Butler and Jeffries:
Extremely strong: D2
Strong: D3, ALPHA1, 5-HT2A
Moderate to moderately strong: D1, D4, ALPHA2
Weak: ACH, H1
Extremely weak: 5-HT1A
Pimozide also inhibits moderately the dopamine-reuptake from the synaptic cleft, accounting for the stimulant properties of the drug. The inhibition of dopamine-reuptake may also explain the synergistic effects of pimozide in the treatment of ADHD when given together with a stimulant.
Contraindications and precautions
Patients with prominent agitation or anxiety
Depressed patients
Severe intoxication with alcohol, opiates, and psychoactive drugs (e.g. antidepressants, benzodiazepines)
Comedication with nefazodone, clarithromycin and vetoconazol (see below under interactions)
Caution: Anticonvulsive treatment in epileptic patients should not be interrupted. Pimozide may in principle lower the seizure-threshold.
Caution: Patients under 18 yrs. of age. Side-effects may be particularly frequent and severe. Treatment should be started with low initial dose and the dose increased very slowly.
In particular, pimozide is known for causing the unpleasant extrapyramidal side-effect akathisia (commonly referred to as "restless pacing") in a large percentage of those who take it. This "restlessness" can sometimes be treated with anticholinergic drugs (mainly benztropine), beta blockers or benzodiazepines, particularly clonazepam (Klonopin). Unfortunately, in many cases this side effect can be so intense that even large doses of these drugs are unable to counter it, and often is so extreme that self-destructive behaviour, including attempting suicide, may occur.
Pimozide has no significant sedative properties, but behaves in some patients as a mild stimulant. If the drug is given shortly before bedtime, insomnia may result. Excitement, agitation, irritability, tension, anxiety, and nightmares have all been seen.
The drug can also cause depression in quite a number of patients, severe enough to result in suicide.
Pimozide has few but nonetheless existing anticholinerg side-effects (e.g. dry mouth, obstipation, urinay hesitancy), rarely of clinical importance.
Pimozide may rarely cause seizures of the grand-mal-type. Patients with epilepsia should be counselled to maintain anticonvulsive therapy.
Particularly disturbing is a relatively high incidence of the long QT syndrome, which may lead to ventricular tachycardia, torsades de pointes and death via ventricular fibrillation.
There is also specific information of carcinogenity both in animals and humans. The carcinogenity in animals has been proven and the carcinogenity in man is strongly suspected (breast cancer and probably liver tumors).
Because of these serious side effects, Pimozide should only be used after the patient has received full information about the drug and agrees to treatment with it despite the risks (fully informed consent).
Interactions
Central Depressants: Action of the other drug may be increased.
Drugs competing for the same cytochrome subenzymes: Risk of mutual and uncontrollable increased action. Nefazodone, Clarithromycin and Vetoconazol all lead to increased pimozide plasma levels and to a higher incidence of (potentially serious) side-effects of pimozide.
Grapefruit juice: Elimination of Pimozide is inhibited. Avoid drinking grapefruit juice during treatment with Pimozide.
Dosage
Due to its long halflife pimozide is usually given once a day (preferably in the morning, because pimozide may have a rather stimulating effect).
Recommended dose ranges are as follows:
Acute psychotic disorders: usually 2 to 12mg daily starting with low doses, than slowly increasing. More than 20mg daily should be avoided, because the benefit-risk ratio is unclear
Chronic psychotic disorders: for maintenance of acute results 6mg daily is the usual dose
Tics: 1 to 16 mg daily in slowly increasing doses
Reactive Depression: 1 to 2mg daily
ADHD: not clearly established, start with very small doses (e.g. 0.5 to 1.0mg) and increase slowly according to the clinical reaction and the side-effects encountered.
Animal toxicity and human overdose
The precise lethal dose in humans is unknown. The oral LD50 is 228 mg/kg in mice, 5120 mg/kg in rats, 188 mg/kg in guinea pigs, and 40 mg/kg in dogs.
Generally human overdoses show exaggerations of the pharmacologic effect of Pimozide. These are : ECG-abnormalities, severe extrapyramidal reactions, hypotension, and comatose state with respiratory depression.
Treatment is largely symptomatic. No specific antidote exists. Induction of emesis, gastric lavage and the repeated application of activated charcoal can all be helpful. Monitor and stabilize, if necessary, the vital functions. Hospitialization and/or admittance to intensive care treatment is in most cases necessary. Due to the long halflife of Pimozide, the symptoms of overdose may last for several days.
References
AFHS Database
Munro, A. (1999) Delusional disorder. Cambridge: Cambridge University Press. ISBN 0-521-58180-X
Van Vloten WA. Pimozide: Use in Dermatology. Dermatol Online J 2003;9(2):3 (fulltext)
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