Zuclopenthixol

Overview

Zuclopenthixol (brand names Cisordinol, Clopixol and others), also known as zuclopentixol, is a medication used to treat schizophrenia and other psychoses. It is classed, pharmacologically, as a typical antipsychotic. Chemically it is a thioxanthene. It is the cis-isomer of clopenthixol (Sordinol, Ciatyl). Clopenthixol was introduced in 1961, while zuclopenthixol was introduced in 1978.[1] WP⚠ Wikipedia itself has flagged this text: citation needed.

Zuclopenthixol is a D₁ and D₂ antagonist, α₁-adrenergic and 5-HT₂ antagonist. While it is approved for use in Australia, Canada, Ireland, India, New Zealand, Singapore, South Africa and the UK, it is not approved for use in the United States.[2][3][4] WP

Uses, dosage and effects

Available forms

Zuclopenthixol is available in three major preparations: WP

• As zuclopenthixol decanoate (Clopixol Depot, Cisordinol Depot), it is a long-acting intramuscular injection. Its main use is as a long-acting injection given every two or three weeks to people with schizophrenia who have a poor compliance with medication and suffer frequent relapses of illness. There is some evidence it may be more helpful in managing aggressive behaviour.[5][6] WP
• As zuclopenthixol acetate (Clopixol-Acuphase, Cisordinol-Acutard), it is a shorter-acting intramuscular injection used in the acute sedation of psychotic inpatients. The effect peaks at 48–72 hours providing 2–3 days of sedation.[7] WP
• As zuclopenthixol dihydrochloride (Clopixol, Cisordinol), it is a tablet used in the treatment of schizophrenia in those who are compliant with oral medication.[8] WP

It is also used in the treatment of acute bipolar mania. WP

Dosing

As a long-acting injection, zuclopenthixol decanoate comes in a 200 mg and 500 mg ampoule. Doses can vary from 50 mg weekly to the maximum licensed dose of 600 mg weekly. In general, the lowest effective dose to prevent relapse is preferred. The interval may be shorter as a patient starts on the medication before extending to 3 weekly intervals subsequently. The dose should be reviewed and reduced if side effects occur, though in the short-term an anticholinergic medication benztropine may be helpful for tremor and stiffness, while diazepam may be helpful for akathisia. 100 mg of zuclopenthixol decanoate is roughly equivalent to 20 mg of flupentixol decanoate or 12.5 mg of fluphenazine decanoate. WP

In oral form zuclopenthixol is available in 2, 10, 25 and 40 mg tablets, with a dose range of 20–60 mg daily.[9] WP

Risks and side effects

Side effects

Chronic administration of zuclopenthixol (30 mg/kg/day for two years) in rats resulted in small, but significant, increases in the incidence of thyroid parafollicular carcinomas and, in females, of mammary adenocarcinomas and of pancreatic islet cell adenomas and carcinomas. An increase in the incidence of mammary adenocarcinomas is a common finding for D₂ antagonists which increase prolactin secretion when administered to rats. An increase in the incidence of pancreatic islet cell tumours has been observed for some other D₂ antagonists. The physiological differences between rats and humans with regard to prolactin make the clinical significance of these findings unclear. WP

Withdrawal syndrome: Abrupt cessation of therapy may cause acute withdrawal symptoms (eg, nausea, vomiting, or insomnia). Symptoms usually begin in 1 to 4 days of withdrawal and subside within 1 to 2 weeks.[10][11] WP

Other permanent side effects are similar to many other typical antipsychotics, namely extrapyramidal symptoms as a result of dopamine blockade in subcortical areas of the brain. This may result in symptoms similar to those seen in Parkinson's disease and include a restlessness and inability to sit still known as akathisia, a slow tremor and stiffness of the limbs. Zuclopenthixol is thought to be more sedating than the related flupentixol, though possibly less likely to induce extrapyramidal symptoms than other typical depots. As with other dopamine antagonists, zuclopenthixol may sometimes elevate prolactin levels; this may occasionally result in amenorrhoea or galactorrhoea in severe cases. Neuroleptic malignant syndrome is a rare but potentially fatal side effect. Any unexpected deterioration in mental state with confusion and muscle stiffness should be seen by a physician.[5][8] WP

Zuclopenthixol decanoate induces a transient dose-dependent sedation. However, if the patient is switched to maintenance treatment with zuclopenthixol decanoate from oral zuclopenthixol or from i.m. zuclopenthixol acetate the sedation will be no problem. Tolerance to the unspecific sedative effect develops rapidly.[12] WP

Very common Adverse Effects (≥10% incidence)[13] WP

• Hypersalivation[13] WP
• Somnolence[13] WP
• Akathisia[13] WP
• Hyperkinesia[13] WP
• Hypokinesia[13] WP

Common (1–10%)[13] WP

• Tachycardia[13] WP
• Heart palpitations[13] WP
• Vertigo[13] WP
• Accommodation disorder[13] WP
• Abnormal vision[13] WP
• Salivary hypersecretion[13] WP
• Constipation[13] WP
• Vomiting[13] WP
• Dyspepsia[13] WP
• Diarrhoea[13] WP
• Asthenia[13] WP
• Fatigue[13] WP
• Malaise[13] WP
• Pain (at the injection site)[13] WP
• Increased appetite[13] WP
• Weight gain[13] WP
• Myalgia[13] WP
• Tremor[13] WP
• Dystonia[13] WP
• Hypertonia[13] WP
• Dizziness[13] WP
• Headache[13] WP
• Paraesthesia[13] WP
• Disturbance in attention[13] WP
• Amnesia[13] WP
• Abnormal gait[13] WP
• Insomnia[13] WP
• Depression[13] WP
• Anxiety[13] WP
• Abnormal dreams[13] WP
• Agitation[13] WP
• Decreased libido[13] WP
• Nasal congestion[13] WP
• Dyspnoea[13] WP
• Hyperhidrosis[13] WP
• Pruritus[13] WP

Uncommon (0.1–1%)[13] WP

• Hyperacusis[13] WP
• Tinnitus[13] WP
• Mydriasis[13] WP
• Abdominal pain[13] WP
• Nausea[13] WP
• Flatulence[13] WP
• Thirst[13] WP
• Injection site reaction[13] WP
• Hypothermia[13] WP
• Pyrexia[13] WP
• Abnormal liver function tests[13] WP
• Decreased appetite[13] WP
• Weight loss[13] WP
• Muscle rigidity[13] WP
• Trismus[13] WP
• Torticollis[13] WP
• Tardive dyskinesia[13] WP
• Hyperreflexia[13] WP
• Dyskinesia[13] WP
• Parkinsonism[13] WP
• Syncope[13] WP
• Ataxia[13] WP
• Speech disorder[13] WP
• Hypotonia[13] WP
• Convulsion[13] WP
• Migraine[13] WP
• Apathy[13] WP
• Nightmares[13] WP
• Libido increased[13] WP
• Confused state[13] WP
• Ejaculation failure[13] WP
• Erectile dysfunction[13] WP
• Female orgasmic disorder[13] WP
• Vulvovaginal[13] WP
• Dryness[13] WP
• Rash[13] WP
• Photosensitivity[13] WP
• Pigmentation disorder[13] WP
• Seborrhoea[13] WP
• Dermatitis[13] WP
• Purpura[13] WP
• Hypotension[13] WP
• Hot flush[13] WP

Rare (0.01–0.1%)[13] WP

• Thrombocytopenia[13] WP
• Neutropenia[13] WP
• Leukopenia[13] WP
• Agranulocytosis[13] WP
• QT prolongation[13] WP
• Hyperprolactinaemia[13] WP
• Hypersensitivity[13] WP
• Anaphylactic reaction[13] WP
• Hyperglycaemia[13] WP
• Glucose tolerance impaired[13] WP
• Hyperlipidaemia[13] WP
• Gynaecomastia[13] WP
• Galactorrhoea[13] WP
• Amenorrhoea[13] WP
• Priapism[13] WP
• Withdrawal symptoms[13] WP

Very rare (<0.01%)[13] WP

• Cholestatic hepatitis[13] WP
• Jaundice[13] WP
• Neuroleptic malignant syndrome[13] WP
• Venous thromboembolism[13] WP

Pharmacology

Pharmacodynamics

Evidence from in vitro work and clinical sources (i.e. therapeutic drug monitoring databases) suggests that both CYP2D6 and CYP3A4 play important roles in zuclopenthixol metabolism.[14] WP⚠ A word may be missing here. It reads this way in the source too.

History

History

Zuclopenthixol was introduced by Lundbeck in 1978.[15] WP

Legal status

Society and culture

A 45‑year‑old Australian man died on 22 May 2019 in Balga from combined drug toxicity while under a community treatment order (CTO) that forced him to receive monthly depot injections of zuclopenthixol decanoate, which he frequently declined. The coroner concluded that, despite the death, the use of compulsory treatment was justified given the patient's "lack of insight" and the absence of alternative facilities.[16] WP

Chemistry

Formula

C22H25ClN2OS PC

CAS number

53772-83-1 PC

Molar mass (g/mol)

401.0 PC

IUPAC name (computed by PubChem)

2-[4-[(3Z)-3-(2-chlorothioxanthen-9-ylidene)propyl]piperazin-1-yl]ethanol PC

SMILES

C1CN(CCN1CC/C=C\2/C3=CC=CC=C3SC4=C2C=C(C=C4)Cl)CCO PC

InChIKey

WFPIAZLQTJBIFN-DVZOWYKESA-N PC

PubChem CID

5311507

Harm reduction information

No harm reduction data is on file for this compound yet. That means no dose, timing or combination data from PsychonautWiki or TripSit. Please don't guess a dose from similar compounds. If you have taken it and feel unwell, contact emergency services or a poison control center.

User reports

Pop culture

No references added yet.

Sources

1. Other Sneader, Walter. Drug discovery: a history. 2005
2. Journal / agency Christensen AV, Arnt J, Hyttel J, Larsen JJ, Svendsen O. Pharmacological effects of a specific dopamine D-1 antagonist SCH 23390 in comparison with neuroleptics. Life Sciences. April 1984. doi:10.1016/0024-3205(84)90607-6 · PMID 6144029
3. Journal / agency Green AI, Noordsy DL, Brunette MF, O'Keefe C. Substance abuse and schizophrenia: pharmacotherapeutic intervention. Journal of Substance Abuse Treatment. January 2008. doi:10.1016/j.jsat.2007.01.008 · PMID 17574793 · PMC2930488
4. Other Martindale: The complete drug reference. 2009
5. Journal / agency da Silva Freire Coutinho E, Fenton M, Quraishi SN. Zuclopenthixol decanoate for schizophrenia. The Cochrane Database of Systematic Reviews. 1999. doi:10.1002/14651858.CD001164 · PMID 10796607 · PMC7032616
6. Journal / agency Haessler F, Glaser T, Beneke M, Pap AF, Bodenschatz R, Reis O. Zuclopenthixol in adults with intellectual disabilities and aggressive behaviours. British Journal of Psychiatry. 2007. doi:10.1192/bjp.bp.105.016535 · PMID 17470962
7. Other Lundbeck P/L. Clopixol Acuphase 50 mg/mL Injection Clopixol Acuphase 100 mg / 2 mL Injection. 1991
8. Journal / agency Bryan EJ, Purcell MA, Kumar A. Zuclopenthixol dihydrochloride for schizophrenia. The Cochrane Database of Systematic Reviews. November 2017. doi:10.1002/14651858.CD005474.pub2 · PMID 29144549 · PMC6486001
9. Other Clopixol 2 mg film-coated tablets - Summary of Product Characteristics (SmPC) - (emc)
10. Other Clopixol 2 mg film-coated tablets - Summary of Product Characteristics (SmPC) - (emc)
11. Other UpToDate
12. Other Summary of Product Characteristics
13. Other TGA eBS - Product and Consumer Medicine Information Licence
14. Journal / agency Davies SJ, Westin AA, Castberg I, Lewis G, Lennard MS, Taylor S, Spigset O. Characterisation of zuclopenthixol metabolism by in vitro and therapeutic drug monitoring studies. Acta Psychiatrica Scandinavica. 2010. doi:10.1111/j.1600-0447.2010.01619.x · PMID 20946203
15. Other William Andrew Publishing. Pharmaceutical Manufacturing Encyclopedia. 22 October 2013
16. Other Inquest into the Death of Boris DRLESKI. 13 April 2022

Text and values on this page are quoted from Wikipedia (CC BY-SA 4.0), PubChem (public domain). Each value links to the exact revision it came from.