Product image of Latomno (Lurasidone) supplied by GNH India

Latomno

Active Ingredient:
Lurasidone
Origin:
EU

Latomno (Lurasidone)

Lurasidone, the active ingredient in Latomno, is an atypical antipsychotic presented as an oral tablet for oral use. It is indicated for the treatment of schizophrenia and bipolar depression in adult patients.

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

Manufacturer / TM Owner

Innovis Pharma

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Indications & Clinical Uses

Lurasidone is an atypical antipsychotic used in psychiatric disorders affecting mood and thought processes.

  • Schizophrenia: reduces psychotic symptoms and lowers risk of relapse.
  • Bipolar depression: alleviates depressive episodes in bipolar I disorder.
  • Schizoaffective disorder (when approved): helps control both mood and psychotic features.

How It Works

  • Lurasidone works by antagonizing dopamine D2 receptors and serotonin 5‑HT2A receptors, while partially agonizing 5‑HT1A receptors and blocking 5‑HT7 receptors. This combined activity modulates dopaminergic and serotonergic neurotransmission, contributing to antipsychotic and mood‑stabilising effects in the central nervous system.

Side Effects

Lurasidone may cause a range of adverse reactions, from mild to serious.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Akathisia: inner restlessness or inability to stay still.
  • Somnolence: increased sleepiness or fatigue.
  • Headache: mild to moderate head pain.
  • Weight gain: modest increase in body weight.
  • Metabolic changes: slight alterations in glucose or lipid levels.

Serious or Rare Side Effects

  • Extrapyramidal symptoms: severe movement disorders.
  • Neuroleptic malignant syndrome: life‑threatening reaction with fever and muscle rigidity.
  • Tardive dyskinesia: persistent involuntary movements.
  • Orthostatic hypotension: marked drop in blood pressure on standing.
  • Seizures: rare occurrence of convulsive episodes.
  • Suicidal ideation: emergence or worsening of suicidal thoughts.

Precautions & Warnings

Before initiating therapy, consider the following safety measures.

  • Cardiovascular assessment: evaluate for QT‑prolongation risk.
  • Metabolic monitoring: check fasting glucose and lipid profile periodically.
  • Pregnancy and lactation: avoid use unless benefits outweigh potential risks.
  • Elderly patients: start at the lowest effective dose and monitor closely.
  • Concomitant CNS depressants: use with caution due to additive sedation.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Lurasidone can interact with several drug classes; awareness of interaction severity guides clinical decisions.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may markedly increase lurasidone plasma levels.
  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may substantially reduce efficacy.

Moderate Interactions (Monitor Closely)

  • CNS depressants (e.g., benzodiazepines, alcohol): may enhance sedation.
  • Antihypertensives: additive effect on blood pressure lowering.
  • Anticholinergic agents: may worsen cognitive side effects.
  • QT‑prolonging drugs (e.g., certain antiarrhythmics): monitor ECG for interval changes.

Frequently Asked Questions

Latomno contains lurasidone, an atypical antipsychotic prescribed for adults with schizophrenia and for the depressive episodes of bipolar I disorder. It helps control psychotic symptoms and improve mood stability when used as part of a comprehensive treatment plan.

Lurasidone blocks dopamine D2 receptors and serotonin 5‑HT2A receptors while partially stimulating 5‑HT1A receptors and antagonising 5‑HT7 receptors. This mixed activity balances dopaminergic and serotonergic pathways, reducing psychosis and depressive symptoms.

The dosage of Latomno is individualized by the prescribing clinician based on the patient’s condition, response, and tolerability. The prescriber determines the appropriate strength and titration schedule, which may be adjusted during treatment.

Safety data for lurasidone in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and decisions should be made in consultation with a healthcare professional.

To request Latomno, 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 any cold‑chain requirements), and necessary import documentation.

Compared with other atypical antipsychotics, lurasidone has a relatively favourable metabolic profile, showing less weight gain and fewer lipid abnormalities. Its receptor binding pattern also offers mood‑stabilising benefits, making it a preferred option for patients needing both antipsychotic and antidepressant effects.

Latomno should be stored at ambient temperature, below 25 °C. Keep the tablets in the original container, protect them from moisture and direct sunlight, and ensure they are out of reach of children.

Latomno is taken orally, usually once daily with food to enhance absorption. The tablet should be swallowed whole with water and not crushed, chewed, or split unless specifically instructed by a healthcare professional.

Serious risks include extrapyramidal symptoms such as severe movement disorders, neuroleptic malignant syndrome—a rare but life‑threatening reaction—and the potential for suicidal thoughts, especially during early treatment. Patients should be monitored closely for any emergent signs.

Latomno is contraindicated in individuals with known hypersensitivity to lurasidone or any of its excipients. Caution is also advised for patients with a history of severe cardiovascular disease, uncontrolled diabetes, or those taking strong CYP3A4 inhibitors or inducers without appropriate dose adjustments.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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