Product image of Lacosamid (Lacosamide) supplied by GNH India

Lacosamid

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamid (Lacosamide)

Lacosamide, the active ingredient in Lacosamid, is an anticonvulsant presented as an oral tablet for oral use. It belongs to the class of sodium‑channel modulators and is indicated for the treatment of partial‑onset seizures in patients with epilepsy, helping to reduce seizure frequency under medical supervision.

GNH India supplies Lacosamid as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable sourcing, regulatory support and consistent product quality to meet the needs of healthcare providers across multiple markets.

Manufacturer / TM Owner

Hexal Ag

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Indications & Clinical Uses

Lacosamide is used in the management of seizure disorders, particularly within the epilepsy therapeutic pathway.

  • Partial‑onset seizures: reduces seizure frequency as adjunctive therapy in epilepsy patients.
  • Epilepsy (generalized): contributes to overall seizure control when combined with other antiepileptic drugs.
  • Refractory epilepsy: offers an alternative mechanism for patients not responding adequately to other treatments.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes, stabilizing hyper‑excitable neuronal membranes and limiting repetitive firing. By selectively modulating the sodium channel’s inactivated state, it reduces the propagation of epileptic discharges without markedly affecting normal neuronal activity, thereby decreasing seizure occurrence. The drug does not significantly alter cardiac conduction at therapeutic doses, and its effect is additive when combined with other antiepileptic agents.

Side Effects

Lacosamide may be associated with a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Nausea: mild to moderate stomach upset.
  • Fatigue: feeling unusually tired or weak.
  • Headache: mild to moderate pain in the head.

Serious or Rare Side Effects

  • Suicidal thoughts: emergence of depressive symptoms or suicidal ideation.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Cardiac arrhythmias: including PR‑interval prolongation or atrioventricular block.
  • Hypersensitivity: anaphylactic reactions or severe rash.

Precautions & Warnings

Before initiating Lacosamide therapy, several safety considerations should be reviewed.

  • Renal impairment: dose adjustment may be required in patients with reduced kidney function.
  • Hepatic impairment: monitor liver function tests and consider dose modification.
  • Cardiac conduction disorders: avoid in patients with pre‑existing PR‑interval prolongation or AV block.
  • Pregnancy: limited data; use only if potential benefit justifies potential risk to fetus.
  • Concomitant antiepileptics: assess for additive CNS depression and adjust therapy as needed.
  • Store at room temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., carbamazepine, phenytoin): may markedly reduce lacosamide plasma levels.
  • Other sodium‑channel blockers (e.g., lamotrigine, oxcarbazepine): increase risk of CNS depression and cardiac effects.
  • QT‑prolonging agents (e.g., amiodarone, erythromycin): may exacerbate cardiac conduction abnormalities.

Moderate Interactions (Monitor Closely)

  • Hormonal contraceptives: lacosamide may reduce contraceptive effectiveness; advise alternative methods.
  • Alcohol: combined use can enhance dizziness and sedation.
  • Other antiepileptic drugs: may require dose adjustments based on therapeutic monitoring.

Frequently Asked Questions

Lacosamid contains the active ingredient lacosamide, an anticonvulsant indicated for the treatment of partial‑onset seizures in patients with epilepsy. It is used as adjunctive therapy to reduce seizure frequency and improve overall seizure control.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes. This stabilises hyper‑excitable neurons, limits repetitive firing, and reduces the spread of epileptic discharges, thereby decreasing the likelihood of seizure events.

The appropriate dose of lacosamide is determined by the prescribing clinician based on the patient’s age, weight, renal and hepatic function, and response to therapy. Dosage regimens are individualized and should follow the prescriber’s instructions.

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

To order Lacosamid, 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 required import documentation.

Lacosamide has a distinct mechanism that enhances slow sodium‑channel inactivation, unlike many older agents that block fast inactivation. This can provide seizure control in patients who have not responded to drugs such as carbamazepine or valproate, while offering a generally favourable tolerability profile.

Lacosamide tablets should be stored at room temperature, below 25 °C, in the original container. Protect them from moisture, excessive heat and direct sunlight to maintain product stability throughout its shelf life.

Lacosamide is administered orally as a tablet, taken with water. It is usually prescribed as an adjunct to existing antiepileptic therapy, and the exact timing and frequency are set by the treating physician.

Serious risks include the potential for suicidal thoughts or behavior, severe skin reactions such as Stevens‑Johnson syndrome, and cardiac conduction abnormalities like PR‑interval prolongation or atrioventricular block. Patients should be monitored closely for these events.

Lacosamide should be avoided in patients with known hypersensitivity to the drug, those with significant cardiac conduction disorders (e.g., existing PR‑interval prolongation), and individuals for whom a reliable contraceptive method cannot be ensured if pregnancy risk is a concern.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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