Product image of Olpinat (Olanzapine) supplied by GNH India

Olpinat

Active Ingredient:
Olanzapine
Origin:
EU

Olpinat (Olanzapine)

Olanzapine, the active ingredient in Olpinat, is an atypical antipsychotic presented as a 10 mg tablet for oral use. It treats schizophrenia and bipolar I disorder in adults and adolescents. GNH India supplies Olpinat as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

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

Manufacturer / TM Owner

Vipharm S.A.

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Indications & Clinical Uses

Olpinat is an atypical antipsychotic that acts on dopamine and serotonin pathways to manage serious mental health conditions.

  • Schizophrenia: reduces positive and negative symptoms and helps maintain long‑term stability.
  • Bipolar I disorder (manic episodes): controls acute mania and supports maintenance therapy.
  • Schizoaffective disorder: alleviates psychotic features and mood symptoms.
  • Psychotic depression: augments antidepressant treatment to improve depressive and psychotic symptoms.
  • Agitation associated with schizophrenia or bipolar disorder: provides rapid calming effect.

How It Works

  • Olanzapine works primarily as an antagonist at dopamine D2 and serotonin 5‑HT2A receptors, with additional affinity for histamine H1, muscarinic, and adrenergic receptors. This receptor profile modulates neurotransmission, reducing dopaminergic overactivity and serotonergic imbalance that underlie psychotic and mood symptoms.

Side Effects

Olpinat may cause a range of adverse reactions, most of which are dose‑dependent and reversible upon discontinuation.

Common Side Effects

  • Weight gain: increased appetite and caloric intake.
  • Sedation: drowsiness or feeling of being slowed down.
  • Dry mouth: reduced salivation.
  • Constipation: slowed gastrointestinal motility.
  • Elevated triglycerides: changes in lipid metabolism.
  • Orthostatic hypotension: drop in blood pressure on standing.

Serious or Rare Side Effects

  • Neuroleptic malignant syndrome: high fever, muscle rigidity, autonomic instability.
  • Hyperglycaemia or new‑onset diabetes mellitus.
  • Tardive dyskinesia: involuntary, repetitive movements.
  • Seizures: especially in patients with pre‑existing seizure disorders.
  • Severe leukopenia or agranulocytosis.
  • Hepatotoxicity: abnormal liver function tests.

Precautions & Warnings

When prescribing Olpinat, clinicians should evaluate patient history and monitor for specific risks.

  • Metabolic monitoring: regularly check weight, fasting glucose, and lipid profile.
  • Cardiovascular assessment: monitor blood pressure and heart rate, especially during initiation.
  • CNS effects: advise patients about sedation and avoid operating heavy machinery until they know how the drug affects them.
  • Pregnancy and lactation: use only if benefits outweigh risks; discuss potential fetal exposure.
  • Elderly patients: start at lower doses and monitor for orthostatic hypotension and falls.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Olpinat can interact with several drug classes, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Strong CYP1A2 inhibitors (e.g., fluvoxamine): may increase olanzapine plasma levels.
  • CNS depressants (benzodiazepines, opioids): additive sedation and respiratory depression.
  • Anticholinergic agents: heightened risk of anticholinergic toxicity.

Moderate Interactions (Monitor Closely)

  • CYP2D6 substrates (e.g., tamoxifen): may reduce conversion to active metabolites.
  • Smoking: induces CYP1A2, potentially lowering olanzapine concentrations.
  • Lithium: combined use may increase risk of neurotoxicity.

Frequently Asked Questions

Olpinat contains olanzapine, an atypical antipsychotic indicated for the treatment of schizophrenia, bipolar I disorder (including manic episodes), schizoaffective disorder, and psychotic depression. It helps control psychotic symptoms such as delusions, hallucinations, and mood instability.

Olanzapine acts as an antagonist at dopamine D2 and serotonin 5‑HT2A receptors, while also affecting histamine, muscarinic, and adrenergic receptors. This mixed receptor activity balances neurotransmitter signaling, reducing the excessive dopaminergic and serotonergic activity that contributes to psychosis and mood swings.

The appropriate dose of Olpinat is determined by a qualified prescriber based on the individual’s condition, age, response, and tolerability. Clinicians start with a low dose and may adjust gradually, following current clinical guidelines and patient monitoring.

Olpinat should be used in pregnancy or while breastfeeding only if the potential benefit justifies the potential risk to the fetus or infant. Clinicians must weigh the risks of untreated psychiatric illness against possible drug‑related effects and discuss these considerations with the patient.

To order Olpinat, 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 and any necessary import documentation.

Compared with first‑generation antipsychotics, Olpinat (olanzapine) generally offers lower rates of extrapyramidal symptoms but has a higher propensity for metabolic side effects such as weight gain and glucose elevation. Relative to other atypicals, its efficacy in treating both psychotic and mood symptoms is comparable, while its side‑effect profile differs.

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

Olpinat is supplied as oral tablets intended for swallowing with water. It is usually taken once daily, with or without food, as directed by the prescribing clinician.

Serious risks include neuroleptic malignant syndrome, significant hyperglycaemia or new‑onset diabetes, tardive dyskinesia, severe leukopenia, and hepatotoxicity. Patients should be monitored regularly for early signs of these conditions, and treatment should be discontinued if they occur.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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