Product image of Paliperidone Teva (Paliperidone Palmitate) supplied by GNH India

Paliperidone Teva

Active Ingredient:
Paliperidone Palmitate
Origin:
EU

Paliperidone Teva (Paliperidone Palmitate)

Paliperidone palmitate, the active ingredient in Paliperidone Teva, is a long‑acting atypical antipsychotic presented as an injectable suspension for intramuscular use. It is indicated for the treatment of schizophrenia in adult patients. GNH India supplies Paliperidone Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

GNH India supplies Paliperidone Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Teva Gmbh

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Indications & Clinical Uses

Paliperidone palmitate is a long‑acting formulation that acts on dopamine and serotonin pathways to manage chronic psychotic disorders.

  • Schizophrenia: Reduces the frequency of psychotic relapses and stabilises mood in adult patients.
  • Schizoaffective disorder: Helps maintain symptom control when oral therapy is insufficient.
  • Maintenance therapy for schizophrenia: Provides consistent plasma levels to minimise breakthrough symptoms between oral dosing intervals.

How It Works

  • Paliperidone palmitate is a pro‑drug of paliperidone that, after intramuscular administration, is slowly hydrolysed to release paliperidone. The active moiety antagonises dopamine D2 and serotonin 5‑HT2A receptors, modulating neurotransmission in mesolimbic and mesocortical pathways and thereby reducing psychotic symptoms.

Side Effects

Paliperidone palmitate may cause a range of adverse reactions, most of which are dose‑dependent and reversible.

Common Side Effects

  • Injection site pain or erythema
  • Headache
  • Drowsiness or somnolence
  • Weight gain
  • Restlessness (akathisia)
  • Dry mouth

Serious or Rare Side Effects

  • Neuroleptic malignant syndrome
  • Tardive dyskinesia
  • Severe orthostatic hypotension
  • Hyperglycaemia or new‑onset diabetes
  • Seizures
  • Elevated prolactin with associated endocrine effects

Precautions & Warnings

When prescribing Paliperidone Teva, clinicians should consider several safety aspects.

  • Cardiovascular assessment: Evaluate for history of arrhythmias or QT prolongation.
  • Metabolic monitoring: Check blood glucose and lipid profiles regularly.
  • Movement disorders: Observe for signs of tardive dyskinesia or akathisia.
  • Pregnancy and lactation: Use only if the potential benefit justifies the risk.
  • Elderly patients: Start at the lowest recommended dose and monitor closely for sedation.
  • Store at ambient temperature: Keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Paliperidone palmitate can interact with other medicines that affect its metabolism or cardiac conduction.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): May increase paliperidone exposure.
  • QT‑prolonging agents (e.g., quinidine, sotalol): Heighten risk of cardiac arrhythmias.

Moderate Interactions (Monitor Closely)

  • CNS depressants (e.g., benzodiazepines, opioids): May enhance sedation.
  • Antihypertensives: May potentiate orthostatic hypotension.
  • Antidiabetic drugs: May require dose adjustment if hyperglycaemia develops.

Frequently Asked Questions

Paliperidone Teva is a long‑acting injectable antipsychotic indicated for the treatment of schizophrenia and for maintenance therapy in adults who require stable plasma concentrations to prevent relapse.

Paliperidone palmitate is a pro‑drug that is hydrolysed after intramuscular injection to release paliperidone, which blocks dopamine D2 and serotonin 5‑HT2A receptors, helping to normalise neurotransmission in brain pathways linked to psychosis.

The dosing regimen for Paliperidone Teva is determined by the prescribing clinician based on the patient’s clinical status, prior response to oral therapy, and approved labeling; no fixed public dose is provided here.

Paliperidone Teva should only be used during pregnancy or lactation if the potential benefit outweighs the risk to the fetus or infant, as safety data are limited and the drug crosses the placenta.

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

Compared with oral atypical antipsychotics, Paliperidone Teva offers a once‑monthly injection that improves adherence and provides steady drug levels, reducing the risk of missed doses that can trigger relapse.

Store the product at ambient temperature, preferably below 25 °C, in its original container, protected from moisture and direct sunlight. Do not freeze.

Paliperidone Teva is given as an intramuscular injection into the deltoid or gluteal muscle by a qualified healthcare professional, following the loading and maintenance schedule outlined in the prescribing information.

Serious risks include neuroleptic malignant syndrome, tardive dyskinesia, significant orthostatic hypotension, hyperglycaemia, seizures, and elevated prolactin levels that may cause endocrine disturbances.

Patients with known hypersensitivity to paliperidone or any formulation component, those with uncontrolled cardiovascular disease, or individuals with a history of severe neuroleptic malignant syndrome should avoid using Paliperidone Teva.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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