Product image of Lacosamide supplied by GNH India

Lacosamide

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamide

Lacosamide, the active ingredient in Lacosamide, is an Anticonvulsant presented as an oral tablet for oral use. It treats partial‑onset seizures in patients with epilepsy.

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

Manufacturer / TM Owner

Consilient Health Limited

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Indications & Clinical Uses

  • Lacosamide is an anticonvulsant indicated for specific seizure types in epilepsy.
  • Partial‑onset seizures: reduces the frequency of focal seizures when used as monotherapy or adjunctive therapy.
  • Primary generalized tonic‑clonic seizures: used as adjunctive therapy to help control seizure episodes in patients with this seizure type.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes, stabilizing hyperexcitable neuronal membranes and decreasing repetitive neuronal firing, which helps to control seizure activity.

Side Effects

Lacosamide may cause a range of adverse reactions, some of which are common and others that are serious or rare.

Common Side Effects

  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Nausea: feeling of stomach upset or urge to vomit.
  • Headache: mild to moderate pain in the head region.
  • Fatigue: unusual tiredness or lack of energy.
  • Blurred vision: temporary visual disturbances.
  • Diplopia: double vision.

Serious or Rare Side Effects

  • Cardiac arrhythmia: irregular heart rhythm, including PR‑interval prolongation.
  • Suicidal ideation: thoughts of self‑harm or suicide.
  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Hepatic injury: signs of liver dysfunction.
  • Anaphylaxis: severe allergic reaction with breathing difficulty.
  • Cardiac conduction abnormalities: including atrioventricular block.

Precautions & Warnings

  • When prescribing Lacosamide, clinicians should consider several safety aspects.
  • Renal impairment: dose may need adjustment and renal function monitoring.
  • Hepatic impairment: monitor liver enzymes and consider dose modification.
  • Cardiac conduction: obtain baseline ECG and monitor for PR‑interval changes.
  • Concomitant antiepileptics: assess for additive CNS effects and adjust doses.
  • Pregnancy and breastfeeding: risk unknown, use only if benefits outweigh risks.
  • Store at ambient temperature: keep below 25°C in original packaging, protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., carbamazepine, phenytoin): may reduce lacosamide levels.
  • Other sodium‑channel blockers (e.g., lamotrigine, oxcarbazepine): increase risk of cardiac effects.
  • Drugs that prolong PR interval (e.g., diltiazem): may exacerbate conduction delays.

Moderate Interactions (Monitor Closely)

  • Oral contraceptives: efficacy may be decreased, consider alternative methods.
  • Anticoagulants (e.g., warfarin): monitor INR for potential changes.
  • CNS depressants (e.g., alcohol, benzodiazepines): may enhance sedation.
  • Antihypertensives: monitor blood pressure for additive effects.
  • Other antiepileptics: dose adjustments may be required based on therapeutic response.

Frequently Asked Questions

Lacosamide is an anticonvulsant medication prescribed to control partial‑onset seizures and, as adjunctive therapy, primary generalized tonic‑clonic seizures in patients with epilepsy.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, stabilising neuronal membranes and reducing repetitive neuronal firing, which helps to prevent seizure activity.

The dosage of Lacosamide is individualized; a qualified prescriber determines the appropriate dose based on the patient’s clinical condition, response, and any relevant laboratory parameters.

The safety of Lacosamide in pregnancy and lactation has not been fully established. It should be used only if the potential benefit justifies the potential risk to the fetus or infant.

To request Lacosamide, 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 necessary import documentation.

Lacosamide’s unique mechanism—enhancing slow sodium‑channel inactivation—differs from many other antiepileptics that act on fast inactivation. This can provide an alternative for patients who have inadequate seizure control with other agents, though individual response varies.

Lacosamide should be stored at ambient temperature, below 25 °C, in its original packaging, protected from moisture and direct sunlight to maintain stability.

Lacosamide is taken orally, usually as a tablet, and should be swallowed with water. The exact administration schedule is set by the prescribing clinician.

Serious risks include cardiac conduction abnormalities such as PR‑interval prolongation, arrhythmias, severe skin reactions, hepatic injury, suicidal thoughts, and rare cases of anaphylaxis. Patients should be monitored for these events.

Lacosamide is contraindicated in patients with known hypersensitivity to the drug or any of its excipients, and it should be used with caution in individuals with significant cardiac conduction disorders, severe renal or hepatic impairment, or uncontrolled arrhythmias.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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