Zentixol A Injection 50 mg/ml contains Zuclopenthixol, a potent typical antipsychotic belonging to the thioxanthene class. It is specifically formulated for parenteral administration and is used in the management of severe psychotic disorders where rapid symptom control is required. The injectable form provides long-acting antipsychotic effects, making it suitable for patients who are non-compliant with oral therapy or require immediate stabilization of acute psychotic episodes.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Typical Antipsychotic
Thioxanthene Derivative
Zuclopenthixol is a dopamine receptor antagonist, primarily acting at D1 and D2 receptors in the central nervous system. By blocking dopaminergic transmission in key areas of the brain, it reduces psychotic symptoms, including hallucinations, delusions, agitation, and aggression. Zuclopenthixol also exhibits antagonistic activity at alpha-adrenergic, histaminergic, and cholinergic receptors, contributing to sedation, reduced anxiety, and calming effects in acutely agitated patients.
The pharmacological profile of Zentixol A allows it to provide sustained antipsychotic action with slower onset of extrapyramidal side effects compared to some other typical antipsychotics, making it particularly useful in acute psychiatric care settings.
Zentixol A Injection is indicated for:
Acute schizophrenia and other psychotic disorders requiring rapid symptom control
Severe agitation, aggression, or hostility in psychotic patients
Non-compliance with oral antipsychotics or when oral administration is not feasible
Long-term maintenance therapy in stabilized patients through depot formulations
Adults: The recommended starting dose is individualized based on severity and prior response to antipsychotics.
For acute agitation, doses are typically administered intramuscularly, with careful monitoring of cardiovascular and central nervous system effects.
Dose titration may be required to achieve optimal symptom control while minimizing adverse effects.
Elderly patients or those with significant hepatic, renal, or cardiac impairment require careful dose adjustment.
Zentixol A should always be administered under the supervision of a qualified healthcare professional.
Known hypersensitivity to Zuclopenthixol or any component of the formulation
Severe cardiovascular disorders, including recent myocardial infarction or arrhythmias
Severe CNS depression or comatose states
Parkinson’s disease with severe motor symptoms
Common side effects include:
Sedation and drowsiness
Orthostatic hypotension, dizziness
Dry mouth, constipation
Extrapyramidal symptoms (tremor, rigidity)
Serious adverse effects may include:
Tardive dyskinesia (long-term risk)
Neuroleptic malignant syndrome (rare but potentially fatal)
Cardiac arrhythmias or myocarditis
Monitor blood pressure, heart rate, and neurological status during treatment
Caution in patients with hepatic or renal impairment, seizure disorders, or elderly individuals
Avoid abrupt discontinuation; tapering may be required to prevent rebound psychosis
Concomitant use with other CNS depressants or alcohol increases sedative effects
Safety in pregnancy has not been established; use only if clearly necessary
Zuclopenthixol may be excreted in breast milk; breastfeeding is not recommended during therapy
Store below 30°C in a dry place
Protect from light
Keep out of reach of children.
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