Product image of Lacosamide Eg (Lacosamide) supplied by GNH India

Lacosamide Eg

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamide Eg (Lacosamide)

Lacosamide, the active ingredient in Lacosamide Eg, is an anti-epileptic presented as an oral dosage form for oral use. It is indicated for the treatment of partial‑onset seizures in patients with epilepsy.
GNH India supplies Lacosamide Eg as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Eg S.P.A.

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Indications & Clinical Uses

Lacosamide is an anti‑epileptic drug used to control focal seizure activity.

  • Partial‑onset seizures (adults): Reduces seizure frequency when added to existing therapy in adult epilepsy patients.
  • Partial‑onset seizures (pediatric ≥4 years): Provides adjunctive seizure control in children four years of age and older.
  • Refractory focal epilepsy: Serves as an adjunctive option for patients whose seizures are not adequately controlled by other medications.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes, which stabilizes hyper‑excitable neurons and diminishes repetitive firing. This modulation reduces the propagation of epileptic discharges without affecting the fast inactivation phase, contributing to its anticonvulsant effect.

Side Effects

Lacosamide may cause a range of adverse reactions.

Common Side Effects

  • Dizziness: Sensation of light‑headedness or unsteadiness.
  • Fatigue: Persistent tiredness or lack of energy.
  • Nausea: Stomach upset often accompanied by an urge to vomit.
  • Headache: Mild to moderate pain in the head region.
  • Blurred vision: Temporary loss of visual clarity.

Serious or Rare Side Effects

  • Cardiac conduction abnormalities: Prolongation of the PR interval that may lead to arrhythmias.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Suicidal thoughts or behavior: Emergence of depressive symptoms or self‑harm ideation.

Precautions & Warnings

Before initiating therapy, consider the following safety measures.

  • Cardiac conduction: Obtain baseline ECG and monitor for PR‑interval changes.
  • Renal impairment: Assess renal function; dose adjustment may be required.
  • Pregnancy: Safety not established; use only if potential benefit outweighs risk.
  • Driving and operating machinery: Counsel patients about possible dizziness or visual disturbances.
  • Concomitant medications: Review all drugs for potential interactions that may affect cardiac or CNS safety.
  • Store below 25°C: Keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Lacosamide can interact with several medicines, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): May increase lacosamide plasma concentrations.
  • Other sodium‑channel blockers (e.g., carbamazepine, phenytoin): Heightened risk of cardiac conduction effects.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inducers (e.g., rifampin, carbamazepine): May reduce lacosamide levels.
  • Concomitant use with antihypertensives: Potential additive hypotensive effect.
  • Alcohol or CNS depressants: May enhance sedation or dizziness.

Frequently Asked Questions

Lacosamide Eg is prescribed as an adjunctive therapy for partial‑onset (focal) seizures in patients with epilepsy. It helps reduce the frequency of seizures when added to existing antiepileptic regimens.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neurons. This stabilizes hyper‑excitable neuronal membranes, limits repetitive firing, and thereby diminishes the spread of epileptic activity.

The prescribing clinician determines the appropriate dose based on the individual’s age, renal function, seizure type, and response to therapy. Dose titration follows professional guidelines and patient‑specific factors.

Safety data in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. It should be used only when the potential benefit justifies any possible risk, after consultation with a healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies 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 traditional sodium‑channel blockers, Lacosamide selectively enhances slow inactivation, offering a distinct mechanism that may be better tolerated in some patients. It is often considered when seizures are not adequately controlled by drugs such as carbamazepine or levetiracetam.

Store the product at temperatures below 25 °C, in its original container, protected from moisture and direct sunlight. Ensure the packaging remains intact until use to maintain product stability.

Lacosamide Eg is taken orally. The tablet should be swallowed whole with a glass of water and can be taken with or without food, according to the prescriber’s instructions.

Serious concerns include cardiac conduction abnormalities such as PR‑interval prolongation, severe skin reactions like Stevens‑Johnson syndrome, and emergence of suicidal thoughts or behavior. Patients should be monitored for these events and seek immediate medical attention if they occur.

Individuals with known hypersensitivity to lacosamide or any excipients, patients with severe cardiac conduction disorders (e.g., advanced AV block), and those for whom the risk outweighs the benefit should avoid this medication. Clinical judgment is essential.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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