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 a 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 that modulates dopamine and serotonin pathways in psychiatric disorders.

  • Schizophrenia: reduces positive and negative psychotic symptoms and helps maintain stability.
  • Bipolar depression: alleviates depressive episodes in bipolar I disorder.
  • Maintenance of schizophrenia: lowers risk of relapse when used as long‑term therapy.

How It Works

  • Lurasidone acts as an antagonist at dopamine D2 and serotonin 5‑HT2A receptors, while partially agonizing 5‑HT1A receptors and antagonizing 5‑HT7 receptors. This combined receptor profile modulates dopaminergic and serotonergic neurotransmission, contributing to antipsychotic and mood‑stabilising effects without excessive dopamine blockade.

Side Effects

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

Common Side Effects

  • Nausea: transient gastrointestinal discomfort.
  • Akathisia: inner restlessness or inability to stay still.
  • Somnolence: drowsiness or fatigue.
  • Headache: mild to moderate intensity.
  • Weight gain: modest increase in body weight.

Serious or Rare Side Effects

  • Neuroleptic malignant syndrome: life‑threatening reaction with fever and muscle rigidity.
  • Tardive dyskinesia: persistent involuntary movements.
  • Seizures: especially in patients with pre‑existing risk.
  • Orthostatic hypotension: dizziness upon standing.
  • Suicidal thoughts: emergence of suicidal ideation.
  • Agranulocytosis: severe drop in white‑blood cell count.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate several safety considerations.

  • Monitor metabolic parameters: regularly check weight, fasting glucose, and lipid profile.
  • Assess for suicidal ideation: especially during early treatment phases.
  • Avoid abrupt discontinuation: taper dose under medical supervision to reduce withdrawal risk.
  • Use caution in cardiovascular disease: monitor blood pressure and ECG for hypotension or arrhythmia.
  • Store at ambient temperature: keep below 25°C in the original container, protect from moisture.

Avoid Interactions

Lurasidone interacts with several drug classes; some require avoidance while others need close monitoring.

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.
  • Other QT‑prolonging antipsychotics: additive risk of cardiac arrhythmias.

Moderate Interactions (Monitor Closely):\n- Serotonergic agents (e.g., SSRIs, SNRIs): potential for serotonin syndrome.

  • CNS depressants (e.g., alcohol, benzodiazepines): enhanced sedation and respiratory depression.
  • Antihypertensive drugs: possible additive hypotensive effect.

Frequently Asked Questions

Latomno contains lurasidone, an atypical antipsychotic approved for the management of schizophrenia and for the treatment of depressive episodes associated with bipolar I disorder in adult patients.

Lurasidone blocks dopamine D2 and serotonin 5‑HT2A receptors while partially stimulating 5‑HT1A receptors and antagonising 5‑HT7 receptors. This mixed activity balances dopaminergic and serotonergic signaling, reducing psychotic symptoms and improving mood.

The prescribed dose of Latomno is determined by the treating clinician based on the patient’s clinical status, response, and tolerability. Dosage adjustments are made according to individual therapeutic needs.

Safety data for lurasidone in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by a qualified 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 and any necessary import documentation.

Compared with many atypical antipsychotics, lurasidone has a relatively low propensity for metabolic side effects such as weight gain and hyperglycaemia, but it may cause more akathisia. Its receptor profile also offers mood‑stabilising benefits useful in bipolar depression.

Latomno tablets should be stored at ambient temperature, below 25 °C, in the original blister pack or container. Keep the product away from moisture and direct sunlight to maintain stability.

Latomno is taken orally, usually once daily with food to enhance absorption. The tablet should be swallowed whole with water and not crushed or chewed.

Serious risks include neuroleptic malignant syndrome, tardive dyskinesia, seizures, orthostatic hypotension, and the emergence of suicidal thoughts. Patients should be monitored closely for any of these events, especially during treatment initiation and dose changes.

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

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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