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 presented as an oral tablet for oral use. It is indicated for the treatment of major depressive disorder in adult patients, helping to restore normal circadian rhythms and improve mood.

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. Customers benefit from consistent product availability and regulatory support across multiple regions.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Agomelatine is used primarily in the treatment of depressive disorders, targeting mood regulation and sleep disturbances.

  • Major depressive disorder (acute phase): alleviates depressive symptoms and improves sleep.
  • Major depressive disorder (maintenance phase): helps prevent relapse and maintain mood stability.
  • Adjunctive treatment of depression with circadian rhythm disruption: supports resynchronization of sleep‑wake cycles.

How It Works

  • Agomelatine acts as an agonist at melatonin MT1 and MT2 receptors, promoting circadian rhythm alignment, while simultaneously antagonizing serotonin 5‑HT2C receptors. This dual action enhances dopaminergic and noradrenergic neurotransmission in brain regions involved in mood regulation, contributing to antidepressant effects without directly influencing serotonin reuptake.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate pain often occurring early in treatment.
  • Nausea: transient stomach upset that usually resolves with continued use.
  • Dizziness: sensation of light‑headedness, particularly when standing quickly.
  • Fatigue: feeling of tiredness that may improve over time.

Serious or Rare Side Effects

  • Liver injury: elevated liver enzymes or hepatitis requiring monitoring.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Suicidal thoughts: emergence or worsening of suicidal ideation, especially at treatment initiation.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate hepatic function and consider patient‑specific risk factors.

  • Liver monitoring: perform baseline and periodic liver function tests during treatment.
  • Hepatic impairment: avoid use in patients with severe liver disease.
  • CYP1A2 inhibitors: use caution when co‑administered with strong inhibitors, as exposure may increase.
  • Pregnancy and lactation: safety not established; avoid unless benefits outweigh risks.
  • Store at ambient temperature below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Agomelatine's metabolism and safety profile can be affected by concomitant medicines.

Major Interactions (Avoid)

  • Strong CYP1A2 inhibitors (e.g., fluvoxamine): may cause toxic plasma levels.
  • Hepatotoxic drugs (e.g., isoniazid): increase risk of liver injury.
  • Combined use with other antidepressants that raise serotonin: potential for serotonin syndrome.

Moderate Interactions (Monitor Closely)

  • CYP1A2 inducers (e.g., rifampicin, smoking): may reduce efficacy.
  • Alcohol: can exacerbate liver toxicity.
  • Caffeine: may modestly increase plasma concentrations.

Frequently Asked Questions

Lamegom contains agomelatine, which is prescribed for the treatment of major depressive disorder in adult patients. It helps alleviate depressive symptoms and normalizes disrupted sleep‑wake cycles, addressing both mood and circadian rhythm abnormalities associated with depression.

Agomelatine works by stimulating melatonin MT1 and MT2 receptors, which realigns the body’s internal clock, and by blocking serotonin 5‑HT2C receptors, leading to increased dopamine and norepinephrine release in brain areas that regulate mood. This combined action produces antidepressant effects.

The dosage of Lamegom is determined by the prescribing clinician based on the individual’s clinical condition, age, liver function and concomitant medications. Only a qualified healthcare professional can set the appropriate dose and treatment schedule.

Safety of agomelatine in pregnancy and lactation has not been established. It is generally avoided unless the potential benefit to the mother outweighs any possible risk to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives with their doctor.

To request 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 selective serotonin reuptake inhibitors, agomelatine targets melatonin receptors and blocks 5‑HT2C receptors, offering a unique mechanism that improves sleep quality while treating depression. It does not typically cause sexual dysfunction or weight gain, but liver monitoring is required, which differs from many other antidepressants.

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

Lamegom is taken orally, usually once daily in the evening, as directed by a healthcare professional. The tablet should be swallowed whole with water and not crushed or chewed.

The most serious risks include potential liver injury, which may be signaled by elevated liver enzymes, and rare severe skin reactions such as Stevens‑Johnson syndrome. Patients should be monitored regularly for hepatic function and any unusual skin changes.

Lamegom is contraindicated in patients with severe hepatic impairment, known hypersensitivity to agomelatine, or those taking strong CYP1A2 inhibitors like fluvoxamine. Caution is also advised for individuals with a history of liver disease or serious skin reactions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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