Product image of Neuleptil (Periciazine) supplied by GNH India

Neuleptil

Active Ingredient:
Periciazine
Origin:
EU

Neuleptil (Periciazine)

Periciazine, the active ingredient in Neuleptil, is a phenothiazine antipsychotic presented as an oral tablet for oral administration. It acts as a dopamine D2 receptor antagonist and is indicated for the treatment of schizophrenia and acute psychotic disorders in adult patients, helping to reduce hallucinations, delusions, and thought disorganization.

GNH India supplies Neuleptil as a licensed, GDP‑compliant international pharmaceutical supplier, providing reliable access to hospitals, pharmacies, and clinics worldwide. The company adheres to stringent quality standards and offers comprehensive logistics support to ensure product integrity throughout the supply chain.

Manufacturer / TM Owner

Teofarma S.R.L.

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Indications & Clinical Uses

Periciazine is used in the phenothiazine class to manage psychotic conditions by modulating dopamine pathways.

  • Schizophrenia: reduces positive symptoms such as hallucinations and delusions, and improves overall mental stability.
  • Acute psychotic disorders: helps control sudden onset psychotic episodes and stabilizes mood and perception.
  • Schizoaffective disorder: alleviates psychotic features when present alongside mood symptoms.

How It Works

  • Periciazine exerts its antipsychotic effect primarily by blocking dopamine D2 receptors in the mesolimbic and mesocortical pathways, decreasing dopaminergic neurotransmission that underlies psychotic symptoms. It also exhibits antagonism at certain serotonin (5‑HT2) and histamine (H1) receptors, contributing to its therapeutic profile and side‑effect spectrum. The blockade reduces overactivity in the nigrostriatal pathway, which may lead to motor side effects, while the combined receptor activity influences sedation and prolactin levels.

Side Effects

Periciazine may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Drowsiness: feeling of sleepiness or reduced alertness.
  • Dry mouth: decreased salivation leading to discomfort.
  • Constipation: slowed gastrointestinal motility.
  • Blurred vision: temporary visual disturbances.
  • Weight gain: increase in body weight over time.
  • Orthostatic hypotension: dizziness upon standing.

Serious or Rare Side Effects

  • Extrapyramidal symptoms: muscle rigidity, tremor, or involuntary movements.
  • Tardive dyskinesia: persistent involuntary facial or limb movements.
  • Neuroleptic malignant syndrome: life‑threatening fever, muscle rigidity, and autonomic instability.
  • Seizures: occurrence of convulsive episodes.
  • Agranulocytosis: severe reduction in white blood cells.
  • Cardiac arrhythmias: irregular heart rhythms.

Precautions & Warnings

When prescribing Periciazine, clinicians should consider several safety precautions to minimize risks.

  • Assess cardiovascular status: evaluate blood pressure and heart rhythm before initiating therapy.
  • Monitor for extrapyramidal signs: observe patients for early movement disorders.
  • Review metabolic profile: check weight, glucose, and lipid levels periodically.
  • Caution in elderly: increased sensitivity to sedation and orthostatic hypotension.
  • Avoid abrupt discontinuation: taper the dose to reduce withdrawal or relapse risk.
  • Store at ambient temperature: keep tablets below 25 °C in the original container, protected from moisture.

Avoid Interactions

Periciazine can interact with other medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • CNS depressants: concurrent use may enhance sedation and respiratory depression.
  • Anticholinergic agents: may worsen cognitive impairment and increase anticholinergic burden.
  • QT‑prolonging drugs: combined effect can raise the risk of cardiac arrhythmias.

Moderate Interactions (Monitor Closely)

  • Dopamine agonists (e.g., levodopa): may reduce antipsychotic effectiveness.
  • CYP2D6 inhibitors (e.g., fluoxetine): can increase Periciazine plasma levels.
  • Antihypertensives: orthostatic hypotension may be amplified.
  • Alcohol: additive central nervous system depression.

Frequently Asked Questions

Neuleptil contains the active ingredient Periciazine and is prescribed to treat schizophrenia and acute psychotic disorders. It helps control symptoms such as hallucinations, delusions, and severe thought disturbances, providing mental stabilization for adult patients.

Periciazine works by blocking dopamine D2 receptors in key brain pathways, reducing excessive dopaminergic activity that contributes to psychotic symptoms. It also antagonises certain serotonin and histamine receptors, which influences its overall therapeutic and side‑effect profile.

The appropriate dose of Neuleptil is determined individually by a qualified prescriber based on the patient’s clinical condition, response, and tolerability. Specific dosing regimens are not disclosed here and should follow the prescribing information provided by the healthcare professional.

Safety data for Periciazine in pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by the treating physician after a careful risk‑benefit assessment.

To request Neuleptil, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Neuleptil (Periciazine) belongs to the phenothiazine class, a typical antipsychotic, whereas many newer agents are atypical antipsychotics with broader receptor profiles. Phenothiazines often have a higher propensity for extrapyramidal side effects but may be effective for patients who respond poorly to atypicals.

Neuleptil tablets should be stored at ambient temperature, preferably below 25 °C, in the original packaging to protect them from moisture and light. Keep the product out of reach of children and do not use after the expiry date.

Neuleptil is taken orally, usually with a glass of water. The tablet should be swallowed whole and not crushed or chewed unless specifically instructed by a healthcare professional.

Serious risks include extrapyramidal symptoms such as severe muscle rigidity, tardive dyskinesia, neuroleptic malignant syndrome, agranulocytosis, and cardiac arrhythmias. Patients should be monitored closely for any signs of these conditions, and immediate medical attention is required if they occur.

Neuleptil is contraindicated in patients with known hypersensitivity to Periciazine or other phenothiazines, those with severe central nervous system depression, and individuals with a history of malignant hyperthermia. Caution is also advised for patients with uncontrolled cardiovascular disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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