Product image of Lacosamid Glenmark (Lacosamide) supplied by GNH India

Lacosamid Glenmark

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamid Glenmark (Lacosamide)

Lacosamide, the active ingredient in Lacosamid, is an Anticonvulsant presented as an oral tablet for oral use. It is indicated for the treatment of partial‑onset seizures in patients with epilepsy, helping to reduce seizure frequency when used as adjunct therapy.

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

Manufacturer / TM Owner

Glenmark Pharmaceuticals S.R.O.

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Indications & Clinical Uses

Lacosamide is an anticonvulsant that acts on neuronal sodium channels to control seizure activity.

  • Partial‑onset seizures: adjunctive therapy that reduces seizure frequency in epilepsy patients.
  • Focal epilepsy: improves seizure control when added to existing antiepileptic regimens.
  • Epilepsy (adjunctive therapy): contributes to overall seizure management as part of combination treatment.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, stabilizing hyperexcitable neuronal membranes and thereby diminishing the propagation of abnormal electrical activity that underlies seizure generation.

Side Effects

Lacosamide may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Nausea: mild gastrointestinal upset.
  • Fatigue: increased tiredness or lack of energy.
  • Headache: mild to moderate cranial pain.
  • Somnolence: tendency to feel sleepy.
  • Diplopia: occasional double vision.

Serious or Rare Side Effects

  • Stevens‑Johnson syndrome: severe skin reaction requiring immediate medical attention.
  • Toxic epidermal necrolysis: life‑threatening skin detachment.
  • Cardiac arrhythmia: irregular heart rhythm, especially in patients with pre‑existing heart disease.
  • Suicidal ideation: emergence of thoughts of self‑harm.
  • Severe hepatic injury: marked liver enzyme elevation or failure.
  • Anaphylaxis: rare allergic reaction with respiratory compromise.

Precautions & Warnings

When prescribing Lacosamide, clinicians should consider several safety aspects.

  • Renal impairment: monitor renal function and adjust dose if needed.
  • Hepatic impairment: use with caution and observe liver enzymes.
  • Pregnancy: risk unknown; prescribe only if benefits outweigh potential fetal risks.
  • Concomitant antiepileptics: assess for additive CNS depression or altered plasma levels.
  • Driving and operating machinery: advise patients about possible dizziness or somnolence.
  • Store at ambient temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Lacosamide can interact with other medicines, influencing efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase Lacosamide exposure.
  • Strong CYP3A4 inducers (e.g., carbamazepine): may reduce therapeutic levels.
  • Other sodium‑channel blockers (e.g., phenytoin): risk of additive cardiac effects.

Moderate Interactions (Monitor Closely)

  • Oral contraceptives: Lacosamide may lower hormonal efficacy.
  • Certain antidepressants (e.g., SSRIs): potential for serotonin syndrome.
  • Alcohol: may enhance central nervous system depression.

Frequently Asked Questions

Lacosamid contains the active ingredient Lacosamide, which is prescribed as an adjunctive treatment for partial‑onset seizures in patients with epilepsy. It helps to lower the frequency of seizures when added to a patient’s existing antiepileptic regimen.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes. By stabilizing hyperexcitable neurons, it reduces the spread of abnormal electrical activity that can trigger seizures, thereby contributing to seizure control.

The dosage of Lacosamid is individualized by the prescribing clinician based on the patient’s medical condition, response to therapy, and other medications. Only a qualified healthcare professional can determine the appropriate dose and titration schedule.

Safety data for Lacosamide in pregnancy and lactation are limited. It should be used only if the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made in consultation with a healthcare provider.

To request Lacosamid, 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.

Lacosamide’s unique mechanism—enhancing slow sodium‑channel inactivation—differs from many traditional antiepileptics that primarily block fast sodium channels or modulate GABA. This distinct action can provide additional seizure control when combined with other agents, especially in patients who have not responded adequately to other therapies.

Lacosamid should be stored at ambient temperature, below 25 °C, in its original container. Keep the product away from moisture, direct sunlight, and extreme heat to maintain its stability and potency throughout its shelf life.

Lacosamid is taken orally, typically as a tablet. It should be swallowed with water and may be taken with or without food, following the dosing schedule prescribed by the treating physician.

Serious adverse events include severe skin reactions such as Stevens‑Johnson syndrome or toxic epidermal necrolysis, cardiac arrhythmias, suicidal thoughts, and rare cases of hepatic injury. Patients should seek immediate medical attention if they notice any alarming symptoms.

Lacosamid is contraindicated in patients with known hypersensitivity to Lacosamide or any of its excipients. Caution is also advised for individuals with significant cardiac conduction abnormalities, severe renal or hepatic impairment, and those taking medications that may cause dangerous interactions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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