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 employed 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

Lacosamide is used in the management of epilepsy, specifically targeting focal seizure activity.

  • Partial‑onset seizures: reduces seizure frequency when added to existing antiepileptic regimens.
  • Focal seizures: provides additional seizure control as an adjunctive agent.
  • Adjunctive therapy in epilepsy: enhances overall seizure management when combined with other approved medications.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, stabilizing hyperexcitable neuronal membranes and diminishing repetitive neuronal firing. By selectively targeting the slow inactivation phase, it reduces the propagation of epileptiform activity without significantly affecting normal neuronal conduction.

Side Effects

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

Common Side Effects

  • Dizziness: transient sensation of light‑headedness or imbalance.
  • Nausea: mild to moderate stomach upset.
  • Fatigue: increased tiredness or lack of energy.
  • Headache: mild to moderate pain in the head region.
  • Blurred vision: temporary visual disturbances.
  • Diplopia: occasional double vision.

Serious or Rare Side Effects

  • Cardiac arrhythmia: irregular heart rhythm requiring medical attention.
  • Suicidal ideation: emergence of thoughts of self‑harm.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hepatic dysfunction: elevated liver enzymes or liver injury.
  • Respiratory depression: slowed breathing, especially with CNS depressants.
  • Anaphylactic reaction: rare but potentially life‑threatening allergic response.

Precautions & Warnings

When prescribing lacosamide, clinicians should consider several safety measures to minimize risk.

  • Monitor cardiac function: obtain baseline ECG and watch for PR‑interval changes.
  • Assess renal function: adjust dosing in patients with significant impairment.
  • Avoid abrupt discontinuation: taper gradually to prevent seizure worsening.
  • Use caution in hepatic impairment: monitor liver enzymes regularly.
  • Pregnancy: risk category unknown; discuss potential benefits and risks with the patient.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • CYP3A4 inhibitors (e.g., ketoconazole): may increase lacosamide plasma levels.
  • CYP3A4 inducers (e.g., rifampin): may reduce lacosamide exposure.
  • Other sodium channel blockers (e.g., carbamazepine): heightened risk of CNS depression.

Moderate Interactions (Monitor Closely)

  • Carbamazepine: may lower lacosamide concentrations, requiring dose adjustment.
  • Anticoagulants (e.g., warfarin): monitor INR for potential changes.
  • Alcohol: can enhance central nervous system effects, increasing dizziness or sedation.

Frequently Asked Questions

Kanilad contains lacosamide, which is prescribed as an adjunctive treatment for partial‑onset (focal) seizures in patients with epilepsy. It is added to existing antiepileptic regimens to help reduce the frequency of breakthrough seizures.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes. This stabilizes hyperexcitable neurons, limits repetitive firing, and thereby diminishes the spread of epileptiform activity without markedly affecting normal nerve conduction.

The appropriate dose of Kanilad is individualized by the prescribing clinician based on the patient’s age, renal function, concomitant medications, and therapeutic response. Dosage adjustments are made according to clinical guidelines and patient monitoring.

The pregnancy safety category for lacosamide is currently unknown. Healthcare providers should weigh potential benefits against possible risks and discuss these considerations with the patient. Breastfeeding decisions should also be made in consultation with a medical professional.

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.

Compared with other sodium‑channel blockers, lacosamide uniquely enhances slow inactivation rather than fast inactivation, offering a distinct mechanism that may benefit patients who have not responded to drugs like carbamazepine or phenytoin. Its side‑effect profile and drug‑interaction potential also differ, influencing individual treatment choices.

Kanilad tablets should be stored at ambient temperature, below 25 °C, in the original packaging to protect them 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 with or without food, as directed by the prescriber. The tablets are swallowed whole with a glass of water. Patients should follow the dosing schedule provided by their healthcare professional.

Serious risks include cardiac arrhythmias such as PR‑interval prolongation, suicidal thoughts or behaviors, severe skin reactions like Stevens‑Johnson syndrome, and rare cases of hepatic injury. Patients should promptly report any chest discomfort, mood changes, skin eruptions, or jaundice to their doctor.

Kanilad is contraindicated in individuals with known hypersensitivity to lacosamide or any of its excipients. Caution is also advised for patients with significant cardiac conduction abnormalities, severe renal impairment, or those taking interacting medications that cannot be safely managed.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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