Product image of Olanzapine Teva (Olanzapine) supplied by GNH India

Olanzapine Teva

Active Ingredient:
Olanzapine
Origin:
EU

Olanzapine Teva (Olanzapine)

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

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Olanzapine is used in psychiatric care to modulate dopaminergic and serotonergic pathways.

  • Schizophrenia: reduces psychotic symptoms such as delusions, hallucinations and thought disorder.
  • Bipolar I disorder (manic episodes): controls acute mania and stabilises mood.
  • Maintenance treatment of bipolar disorder: helps prevent recurrence of manic or depressive episodes.

How It Works

  • Olanzapine exerts its antipsychotic effect primarily by antagonising dopamine D2 receptors and serotonin 5‑HT2A receptors, while also modulating activity at histamine H1, muscarinic M1‑M5 and adrenergic α1 receptors, resulting in altered neurotransmission across multiple pathways involved in mood and psychosis.

Side Effects

Olanzapine may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Weight gain: increased appetite leading to body mass increase.
  • Somnolence: drowsiness or sedation.
  • Dry mouth: reduced salivation.
  • Constipation: slowed gastrointestinal motility.
  • Dizziness: light‑headed feeling, especially on standing.
  • Increased appetite: heightened desire for food.

Serious or Rare Side Effects

  • Neuroleptic malignant syndrome: life‑threatening reaction with fever and muscle rigidity.
  • Agranulocytosis: severe reduction in white blood cells.
  • Hyperglycemia/diabetes mellitus: marked elevation of blood glucose.
  • Tardive dyskinesia: involuntary, repetitive movements.
  • Leukopenia: lowered white blood cell count.
  • Seizures: risk of convulsive episodes.

Precautions & Warnings

When prescribing Olanzapine, clinicians should consider several safety measures.

  • Metabolic monitoring: regularly assess weight, glucose and lipid levels.
  • Cardiovascular risk: evaluate patients with existing heart disease.
  • Hypersensitivity: avoid use in individuals with known allergy to olanzapine.
  • Elderly dementia patients: increased risk of mortality; use with caution.
  • Hepatic function: adjust use in patients with liver impairment.
  • Store at below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • CNS depressants: may enhance sedation and respiratory depression.
  • Anticholinergic agents: can worsen anticholinergic burden.
  • CYP1A2 inhibitors (e.g., fluvoxamine): increase olanzapine plasma concentrations.
  • CYP1A2 inducers (e.g., smoking): reduce olanzapine levels, risking loss of efficacy.
  • QT‑prolonging drugs: may increase risk of cardiac arrhythmias.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: additive hypotensive effect.
  • Antidiabetic agents: may require dose adjustment due to metabolic changes.
  • Lithium: potential for increased neurotoxicity.
  • SSRIs: heightened risk of serotonin syndrome.
  • Anticholinergic medications: monitor for excessive anticholinergic effects.

Frequently Asked Questions

Olanzapine Teva is prescribed for adults with schizophrenia to reduce psychotic symptoms, and for bipolar I disorder to manage acute manic episodes and to maintain mood stability over the long term.

Olanzapine works by blocking dopamine D2 receptors and serotonin 5‑HT2A receptors, while also influencing histamine, muscarinic and adrenergic receptors, which together modulate neurotransmission linked to mood, perception and cognition.

The specific dose and titration schedule are determined by the prescribing clinician based on the patient’s diagnosis, severity of symptoms, prior treatment response and individual tolerability.

Olanzapine is classified as pregnancy category C; it should only be used if the potential benefit justifies the potential risk to the fetus. It is excreted in breast milk, so breastfeeding is generally not recommended while on therapy.

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.

Olanzapine offers strong efficacy for both psychotic and mood symptoms but is associated with higher rates of weight gain and metabolic changes compared with some alternatives such as aripiprazole or ziprasidone, which may have more favourable metabolic profiles.

Store Olanzapine Teva tablets at temperatures below 25 °C, in the original packaging, and protect them from moisture and direct sunlight to maintain product stability.

Olanzapine Teva is taken orally, usually once daily, with or without food, as directed by the prescriber. Swallow the tablet whole; do not crush or chew unless specifically instructed.

Serious risks include neuroleptic malignant syndrome, severe hyperglycemia or new‑onset diabetes, agranulocytosis, and tardive dyskinesia. Patients should be monitored regularly for signs of these conditions.

Olanzapine should be avoided in individuals with known hypersensitivity to the drug, in patients with severe central nervous system depression, and in elderly patients with dementia‑related psychosis due to an increased risk of mortality.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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