Product image of Lamegom (Agomelatine) supplied by GNH India

Lamegom

Active Ingredient:
Agomelatine
Origin:
EU

Lamegom (Agomelatine)

Agomelatine, the active ingredient in Lamegom, is a melatonin receptor agonist and 5‑HT2C antagonist presented as a tablet for oral use. It is indicated for the treatment of major depressive disorder in adult patients, helping to restore normal circadian rhythm and mood balance.

GNH India supplies Lamegom as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution across multiple regulatory jurisdictions and ensures timely delivery.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Agomelatine is indicated for the treatment of major depressive disorder in adult patients. By targeting melatonin and serotonergic pathways, it addresses mood symptoms and disrupted sleep‑wake cycles, offering a therapeutic option distinct from traditional antidepressants.

  • Major depressive disorder: reduces depressive symptoms and helps normalize circadian rhythm.
  • Maintenance therapy after remission: may support continued mood stability and regular sleep patterns.

How It Works

  • Agomelatine acts as an agonist at the MT1 and MT2 melatonin receptors, which resynchronises the circadian clock, and as an antagonist at the 5‑HT2C serotonin receptor, leading to increased dopaminergic and noradrenergic transmission in the frontal cortex. This combined action restores normal sleep‑wake cycles and modulates mood‑related neurotransmission, contributing to its antidepressant effect. The drug does not significantly inhibit monoamine reuptake, distinguishing it from many conventional antidepressants.

Side Effects

Agomelatine is generally well tolerated, but like all medicines it may cause adverse reactions.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Nausea: transient gastrointestinal upset.
  • Dizziness: may occur especially on standing.
  • Insomnia: occasional difficulty falling asleep.
  • Fatigue: feeling of tiredness during the day.
  • Elevated liver enzymes: mild, usually reversible.

Serious or Rare Side Effects

  • Hepatotoxicity: severe liver injury requiring monitoring.
  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Suicidal thoughts: emergence of suicidal ideation.
  • Allergic reactions: rash, angioedema, or anaphylaxis.
  • QT prolongation: potential cardiac arrhythmia.
  • Pancreatitis: inflammation of the pancreas.

Precautions & Warnings

When prescribing agomelatine, several safety considerations should be observed.

  • Liver function monitoring: baseline and periodic liver enzyme tests are recommended.
  • Alcohol consumption: avoid excessive alcohol as it may increase liver risk.
  • Pregnancy and lactation: use only if benefits outweigh risks; data are limited.
  • Concomitant CYP1A2 inhibitors: avoid or adjust dose as they can raise agomelatine levels.
  • Driving and machinery: may cause dizziness; assess before operating.
  • Store at ambient temperature: keep below 25 °C, in the original pack, protect from moisture.

Avoid Interactions

Agomelatine can interact with other medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Strong CYP1A2 inhibitors (e.g., fluvoxamine, ciprofloxacin): can markedly increase plasma levels.
  • Hepatotoxic drugs (e.g., isoniazid, valproate): raise risk of liver injury.
  • Other serotonergic antidepressants: may increase risk of serotonin syndrome.

Moderate Interactions (Monitor Closely)

  • CYP1A2 inducers (e.g., smoking, carbamazepine): may reduce efficacy.
  • Oral contraceptives: may increase agomelatine exposure.
  • Anticoagulants (e.g., warfarin): monitor INR as agomelatine may affect metabolism.

Frequently Asked Questions

Lamegom contains agomelatine, which is prescribed for the treatment of major depressive disorder in adult patients. It works by resynchronising circadian rhythms and modulating serotonergic pathways, helping to alleviate depressive symptoms and improve sleep quality.

Agomelatine acts as an agonist at melatonin MT1 and MT2 receptors, resetting the body’s internal clock, and as an antagonist at the 5‑HT2C serotonin receptor, which increases dopamine and norepinephrine release in the frontal cortex. This dual action supports mood regulation and normal sleep‑wake cycles.

The dosage of Lamegom is determined by the prescribing clinician based on the patient’s clinical condition, response, and safety considerations. The prescriber will select the appropriate strength and dosing schedule according to current treatment guidelines.

Safety data for agomelatine in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To order Lamegom, 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.

Unlike many conventional antidepressants that primarily inhibit serotonin reuptake, agomelatine targets melatonin receptors and blocks 5‑HT2C receptors. This unique mechanism can improve sleep disturbances and has a different side‑effect profile, making it an alternative for patients who may not tolerate typical SSRIs or SNRIs.

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

Lamegom is taken orally, usually once daily in the evening, with or without food as directed by the prescribing physician. Swallow the tablet whole with a glass of water; do not crush or chew it.

The most serious risks include potential liver injury, severe skin reactions such as Stevens‑Johnson syndrome, and the emergence of suicidal thoughts or behaviors. Regular liver function monitoring and close clinical observation are essential during treatment.

Lamegom is contraindicated in patients with severe hepatic impairment, known hypersensitivity to agomelatine, or those taking strong CYP1A2 inhibitors such as fluvoxamine. It should also be used with caution in individuals with a history of liver disease or significant cardiac conditions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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