Product image of Latuda (Lurasidone) supplied by GNH India

Latuda

Active Ingredient:
Lurasidone
Origin:
EU

Latuda (Lurasidone)

Lurasidone, the active ingredient in Latuda, is a atypical antipsychotic presented as a tablet for oral use. It is indicated for the treatment of schizophrenia and for depressive episodes associated with bipolar I disorder in adult patients. The medication works by modulating dopamine and serotonin pathways to improve psychotic symptoms and mood stability.

GNH India supplies Latuda as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable global distribution.

Manufacturer / TM Owner

Angelini Pharma S.P.A.

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Indications & Clinical Uses

Lurasidone is used in psychiatric disorders that involve dopamine and serotonin dysregulation.

  • Schizophrenia: reduces positive and negative symptoms, improving overall functioning.
  • Bipolar I disorder (depressive episodes): alleviates depressive symptoms and helps maintain mood stability.

How It Works

  • Lurasidone acts as an antagonist at dopamine D2 and serotonin 5‑HT2A receptors, while partially agonizing 5‑HT1A and antagonizing 5‑HT7 receptors. This combined activity balances dopaminergic and serotonergic neurotransmission, leading to reduced psychotic symptoms and stabilization of mood in affected patients.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Akathisia: inner restlessness or urge to move.
  • Somnolence: increased sleepiness or fatigue.
  • Weight gain: modest increase in body weight.
  • Insomnia: difficulty falling or staying asleep.

Serious or Rare Side Effects

  • Neuroleptic malignant syndrome: rare but life‑threatening reaction with fever and muscle rigidity.
  • Tardive dyskinesia: persistent involuntary movements, potentially irreversible.
  • Seizures: occasional occurrence, especially in predisposed individuals.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety aspects.

  • Cardiovascular assessment: evaluate for orthostatic hypotension and QT‑interval prolongation risk.
  • Metabolic monitoring: regularly check weight, glucose, and lipid levels.
  • Hepatic function: adjust use in patients with moderate liver impairment.
  • Suicidal ideation: monitor for emergence of suicidal thoughts, particularly early in treatment.
  • Discontinuation: avoid abrupt cessation to reduce risk of relapse or withdrawal phenomena.
  • Store at ambient temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may markedly increase lurasidone plasma levels.
  • Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine): can substantially reduce drug exposure.
  • Other antipsychotics: concurrent use may heighten the risk of QT prolongation and extrapyramidal symptoms.

Moderate Interactions (Monitor Closely)

  • Anticholinergic agents: may exacerbate dry mouth and constipation.
  • CNS depressants (e.g., benzodiazepines, alcohol): can increase sedation and impair psychomotor performance.
  • Antihypertensive drugs: additive hypotensive effects may occur.

Frequently Asked Questions

Latuda (lurasidone) is prescribed for adults with schizophrenia to reduce psychotic symptoms, and for depressive episodes associated with bipolar I disorder to improve mood and functional outcomes.

Lurasidone blocks dopamine D2 and serotonin 5‑HT2A receptors while partially stimulating 5‑HT1A and blocking 5‑HT7 receptors, helping to rebalance neurotransmitter activity that underlies psychosis and mood disturbances.

The specific dose of Latuda is determined by the prescribing clinician based on the individual’s diagnosis, severity, and response to therapy. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Latuda is classified as Pregnancy Category B, indicating no proven risk in animal studies but limited human data. It should be used only if the potential benefit justifies the potential risk, and breastfeeding decisions should be made in consultation with a healthcare professional.

To request Latuda, 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 many atypical antipsychotics, lurasidone has a relatively favorable metabolic profile, showing lower propensity for weight gain and glucose elevation, while offering comparable efficacy for schizophrenia and bipolar depression.

Latuda tablets should be stored at ambient temperature, below 25 °C, in the original container to protect them from moisture and light. Keep the medication out of reach of children.

Latuda is taken orally as a tablet, usually once daily with food to enhance absorption. Patients should swallow the tablet whole and not split or crush it unless directed by a healthcare professional.

Serious risks include neuroleptic malignant syndrome, tardive dyskinesia, seizures, and significant orthostatic hypotension. Patients should be monitored for signs such as high fever, muscle rigidity, involuntary movements, or fainting.

Latuda is contraindicated in individuals with known hypersensitivity to lurasidone or any of its excipients. Caution is advised for patients with severe hepatic impairment, uncontrolled cardiovascular disease, or a history of neuroleptic malignant syndrome.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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