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

Manufacturer / TM Owner

Norton Waterford T/A Ivax Pharmaceuticals Ireland

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Indications & Clinical Uses

Paliperidone palmitate is a dopamine‑serotonin antagonist used in chronic psychotic disorders.

  • Schizophrenia: maintenance therapy to reduce relapse and control psychotic symptoms.
  • Schizoaffective disorder: management of psychotic features alongside mood symptoms.
  • Maintenance after acute episode: provides sustained drug levels to support long‑term stability.

How It Works

  • Paliperidone palmitate exerts its antipsychotic effect by antagonizing dopamine D2 receptors and serotonin 5‑HT2A receptors in the central nervous system, thereby modulating neurotransmission linked to psychosis. The long‑acting formulation releases the active moiety slowly after intramuscular injection, maintaining therapeutic plasma concentrations for up to a month.

Side Effects

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

Common Side Effects

  • Injection site pain: mild to moderate discomfort at the injection site.
  • Weight gain: gradual increase in body weight.
  • Akathisia: inner restlessness or inability to stay still.
  • Drowsiness: somnolence or reduced alertness.
  • Constipation: decreased bowel movements.
  • Elevated prolactin: hormonal changes leading to menstrual disturbances or galactorrhea.

Serious or Rare Side Effects

  • Neuroleptic malignant syndrome: life‑threatening reaction with fever and muscle rigidity.
  • Tardive dyskinesia: persistent involuntary movements.
  • Seizures: increased risk in susceptible individuals.
  • Orthostatic hypotension: sudden drop in blood pressure upon standing.
  • Hyperglycemia: elevated blood glucose levels.
  • Cardiovascular events: arrhythmias or myocardial infarction.

Precautions & Warnings

Before initiating therapy with Paliperidone Teva, clinicians should evaluate patient history and monitor for specific risks.

  • Cardiovascular disease: assess for history of arrhythmias or heart failure.
  • Metabolic disorders: monitor weight, glucose, and lipid profiles regularly.
  • Pregnancy: avoid use unless benefits outweigh potential fetal risks.
  • Breastfeeding: contraindicated as drug is excreted in milk.
  • Elderly patients: start at lower dose and observe for orthostatic hypotension.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Paliperidone palmitate can interact with several medication classes, altering efficacy or safety.

Major Interactions (Avoid)

  • CYP3A4 inhibitors (e.g., ketoconazole): may increase paliperidone levels and toxicity.
  • CNS depressants (e.g., benzodiazepines): can enhance sedation and respiratory depression.

Moderate Interactions (Monitor Closely):\n- CYP3A4 inducers (e.g., carbamazepine): may reduce drug exposure, risking loss of efficacy.

  • Antihypertensives: additive orthostatic hypotension may occur.
  • Anticholinergic agents: may exacerbate cognitive side effects.

Frequently Asked Questions

Paliperidone Teva is indicated for the long‑term management of schizophrenia and schizoaffective disorder in adult patients. It helps maintain symptom control and reduces the risk of relapse when administered as a monthly intramuscular injection.

Paliperidone palmitate blocks dopamine D2 and serotonin 5‑HT2A receptors in the brain, which moderates neurotransmitter activity linked to psychosis. The depot formulation releases the drug slowly after injection, providing stable plasma concentrations for up to four weeks.

The dosage of Paliperidone Teva is individualized by the prescribing clinician based on the patient’s clinical response, prior treatment history, and tolerability. The prescriber determines the appropriate injection strength and interval.

Paliperidone Teva should be avoided during pregnancy unless the potential benefit justifies the risk to the fetus. It is also contraindicated while breastfeeding because the drug is excreted in breast milk and may affect the infant.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying 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 (including cold‑chain if needed), and required import documentation.

Compared with oral atypical antipsychotics, Paliperidone Teva offers a once‑monthly injection, improving adherence for patients who have difficulty with daily oral dosing. Its efficacy is similar to other long‑acting formulations, but the side‑effect profile may differ, especially regarding injection‑site reactions and prolactin elevation.

Paliperidone Teva must be stored refrigerated at 2‑8 °C. Keep the vials in their original packaging, protect them from light, and do not freeze or shake the product. If the temperature rises above the recommended range, the product should not be used.

Paliperidone Teva is given as an intramuscular injection into the deltoid or gluteal muscle by a qualified healthcare professional. The injection is typically administered once every four weeks after an initial loading phase, as directed by the prescriber.

Serious risks include neuroleptic malignant syndrome, tardive dyskinesia, seizures, significant orthostatic hypotension, and hyperglycemia. Patients should be monitored regularly for these events, and treatment should be discontinued if any life‑threatening reaction occurs.

Paliperidone Teva is contraindicated in patients with known hypersensitivity to paliperidone or any excipients, in those who are pregnant or breastfeeding without a clear benefit, and in individuals with severe cardiovascular instability where the drug may exacerbate hypotension.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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