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

Lacosamide Sandoz

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamide Sandoz (Lacosamide)

Lacosamide, the active ingredient in Lacosamide Sandoz, is an anti‑epileptic presented as an oral tablet for oral use. It is used as adjunctive therapy to reduce the frequency of partial‑onset seizures in patients with epilepsy. It belongs to the class of sodium channel modulators and is indicated for patients whose seizures are not adequately controlled by other antiepileptic drugs.

GNH India supplies Lacosamide Sandoz as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable supply chains across multiple continents.

Manufacturer / TM Owner

Sandoz N.V.

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Indications & Clinical Uses

Lacosamide is an anti‑epileptic drug used as adjunctive therapy for focal seizure disorders.

  • Partial‑onset (focal) seizures: Reduces seizure frequency when added to existing antiepileptic therapy.
  • Focal seizures with secondary generalization: Helps control seizure spread in patients with refractory epilepsy.
  • Adjunctive therapy in epilepsy: Improves overall seizure management for patients not adequately controlled by monotherapy.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, stabilizing neuronal membranes and reducing repetitive neuronal firing. It also binds to collapsin response mediator protein‑2 (CRMP‑2), a protein involved in neuronal development and axonal guidance, thereby modulating neuronal excitability and contributing to its anticonvulsant effect.

Side Effects

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

Common Side Effects

  • Dizziness: Light‑headed sensation, often occurring at treatment initiation.
  • Headache: Mild to moderate intensity, usually transient.
  • Nausea: Gastrointestinal discomfort that may improve with continued use.
  • Fatigue: Generalized tiredness or reduced energy levels.

Serious or Rare Side Effects

  • Cardiac conduction abnormalities: PR‑interval prolongation that can lead to arrhythmias.
  • Suicidal thoughts or behavior: Emergence of depressive symptoms or suicidal ideation.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis, requiring immediate medical attention.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for potential complications.

  • Renal impairment: Adjust dose if severe kidney dysfunction is present.
  • Hepatic impairment: Use with caution in patients with liver disease.
  • Cardiac conduction: Monitor ECG for PR‑interval prolongation.
  • Concomitant antiepileptic drugs: Assess for additive CNS depression.
  • Pregnancy and lactation: Use only if benefit outweighs risk.
  • Store at ambient temperature: Keep below 25 °C, protect from moisture and light in original packaging.

Avoid Interactions

Lacosamide can interact with several medicines, requiring careful assessment.

Major Interactions (Avoid)

  • Concomitant use with strong CYP3A4 inducers (e.g., carbamazepine, phenytoin): May reduce lacosamide plasma levels.
  • Co‑administration with other sodium channel blockers (e.g., lamotrigine, oxcarbazepine): Increases risk of CNS depression.
  • Combination with drugs that prolong PR interval (e.g., verapamil): May cause cardiac conduction abnormalities.

Moderate Interactions (Monitor Closely)

  • Use with other antiepileptic drugs (e.g., valproate, topiramate): May require dose adjustments.
  • Concurrent use of alcohol or CNS depressants: May enhance dizziness and sedation.
  • Interaction with anticoagulants (e.g., warfarin): Monitor INR as lacosamide may affect bleeding risk.

Frequently Asked Questions

Lacosamide Sandoz is prescribed as an adjunctive therapy for partial‑onset (focal) seizures in patients with epilepsy whose seizures are not fully controlled by other antiepileptic medications. It is intended to be added to an existing regimen to improve overall seizure control.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, which stabilises neuronal membranes and reduces repetitive firing. Additionally, it binds to the protein CRMP‑2, influencing neuronal excitability and contributing to its anticonvulsant activity.

The dose is individualized by the prescribing clinician based on the patient’s seizure type, response, and tolerability. Typical titration starts with a low dose that is gradually increased, but the exact regimen must be set by a qualified health professional.

Safety data are limited. Lacosamide should be used during pregnancy or lactation only when the potential benefit to the mother outweighs any potential risk to the fetus or infant. Decisions should be made by the treating physician in consultation with the patient.

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 many traditional sodium‑channel blockers, lacosamide selectively enhances slow inactivation, which may result in a different side‑effect profile. It can be combined with a broad range of other antiepileptics and is often chosen for patients with refractory focal seizures despite other therapies.

Store at ambient temperature below 25 °C, in the original container, protected from moisture and light. Keep the product out of reach of children and do not use it after the expiry date printed on the packaging.

The medication is taken orally, usually as a tablet, with or without food as directed by the prescriber. Swallow the tablet whole; the dosing schedule and any titration steps should follow the clinician’s instructions.

Serious adverse events include cardiac conduction abnormalities such as PR‑interval prolongation, severe skin reactions like Stevens‑Johnson syndrome, and psychiatric effects including suicidal ideation. Patients should be monitored for these signs and seek immediate medical attention if they occur.

Individuals with known hypersensitivity to lacosamide or any of its excipients, patients with severe cardiac conduction disorders, and anyone for whom the prescriber determines that the risks outweigh the benefits should avoid using this medication.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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