Product image of Kanilad (Lacosamide) supplied by GNH India

Kanilad

Active Ingredient:
Lacosamide
Origin:
EU

Kanilad (Lacosamide)

Lacosamide, the active ingredient in Kanilad, is a sodium channel blocker presented as an oral tablet for oral use. It is used as adjunctive therapy for partial‑onset seizures in patients with epilepsy.
GNH India supplies Kanilad as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Medochemie Ltd.

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Indications & Clinical Uses

Kanilad, a sodium channel blocker, is employed in the management of seizure disorders.

  • Partial‑onset seizures: Reduces seizure frequency when added to existing antiepileptic regimens.
  • Focal epilepsy: Helps achieve better overall seizure control in patients with focal seizure types.
  • Epilepsy (adjunctive therapy): Contributes to improved seizure management as part of a comprehensive treatment plan.

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. This modulation reduces the likelihood of seizure initiation and propagation without significantly affecting normal neuronal activity.

Side Effects

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

Common Side Effects

  • Dizziness: A sensation of light‑headedness or unsteadiness.
  • Headache: Mild to moderate pain in the head region.
  • Nausea: Feeling of stomach upset or urge to vomit.
  • Fatigue: Unusual tiredness or lack of energy.
  • Blurred vision: Temporary visual disturbances.
  • Diplopia: Double vision.

Serious or Rare Side Effects

  • Suicidal thoughts or behavior: Emergence of depressive symptoms or suicidal ideation.
  • Severe skin reactions: Including Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Cardiac arrhythmias: Irregular heart rhythms, especially in patients with pre‑existing conduction disorders.
  • Respiratory depression: Marked slowing of breathing.
  • Anaphylaxis: Acute allergic reaction with potential airway compromise.
  • Liver injury: Elevated liver enzymes or hepatitis.

Precautions & Warnings

When prescribing or dispensing Kanilad, consider the following safety measures.

  • Renal impairment: Assess kidney function and adjust therapy if necessary.
  • Hepatic impairment: Monitor liver enzymes regularly.
  • Concomitant antiepileptics: Observe for increased central nervous system side effects.
  • Cardiac conduction disorders: Use with caution in patients with known arrhythmias.
  • Pregnancy: Potential risks are unknown; discuss benefits and risks with a healthcare professional.
  • Store at room temperature: Keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lacosamide can interact with several medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., carbamazepine, phenytoin): May lower lacosamide plasma levels.
  • Other sodium channel blockers (e.g., lamotrigine, phenytoin): May increase neurotoxicity.
  • QT‑prolonging agents (e.g., quinidine, erythromycin): Heightened risk of cardiac arrhythmias.

Moderate Interactions (Monitor Closely)

  • Oral contraceptives: May reduce contraceptive effectiveness; consider alternative methods.
  • Combination with other antiepileptics: May increase dizziness or somnolence.
  • Alcohol: Can enhance central nervous system depression and impair coordination.

Frequently Asked Questions

Kanilad contains lacosamide and is prescribed as an adjunctive treatment for partial‑onset seizures in patients with epilepsy. It helps reduce the frequency of seizures when added to a stable antiepileptic regimen, supporting overall seizure control.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neurons. By stabilizing hyperexcitable neuronal membranes, it diminishes repetitive firing that can trigger seizures, thereby contributing to seizure suppression.

The appropriate dose of Kanilad is determined by the prescribing clinician based on the patient’s individual condition, response, and tolerability. Dosage adjustments are made according to clinical judgment and monitoring.

Safety data for lacosamide in pregnancy and lactation are limited. The potential benefits and risks should be evaluated by a healthcare professional, and the drug should only be used if clearly needed and after discussing alternatives.

To request Kanilad, 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.

Kanilad (lacosamide) belongs to the sodium channel blocker class, offering a distinct mechanism that enhances slow inactivation of sodium channels. Compared with drugs that target fast inactivation, lacosamide may provide better tolerability for some patients, though individual response varies.

Kanilad should be stored at room temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and avoid storing in humid or excessively hot environments.

Kanilad is taken orally, usually as a tablet, with or without food as directed by the prescriber. The medication should be swallowed whole with water and not crushed or chewed unless specifically instructed.

Serious risks include the potential for suicidal thoughts or behavior, severe skin reactions such as Stevens‑Johnson syndrome, cardiac arrhythmias, respiratory depression, anaphylaxis, and liver injury. Patients should seek immediate medical attention if any of these occur.

Kanilad is contraindicated in patients with known hypersensitivity to lacosamide or any of its excipients. Caution is advised for individuals with significant cardiac conduction disorders, severe hepatic impairment, or those taking interacting medications that could increase toxicity.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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