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

Lacosamide Krka

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamide Krka (Lacosamide)

Lacosamide, the active ingredient in Lacosamide Krka, is a sodium channel blocker presented as an oral tablet for oral use. It treats partial‑onset seizures and epilepsy in adults and children.

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

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Lacosamide is an antiepileptic drug that modulates neuronal excitability in seizure disorders.

  • Partial‑onset seizures: reduces seizure frequency when used as adjunct therapy.
  • Epilepsy (refractory): provides additional seizure control in patients not fully managed by other agents.
  • Adjunctive therapy for focal epilepsy: enhances overall seizure management when combined with other antiepileptics.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, stabilizing neuronal membranes and decreasing hyper‑excitability. By selectively targeting the persistent sodium current, it limits repetitive neuronal firing that underlies seizure activity, without markedly affecting normal neuronal conduction.

Side Effects

Lacosamide may cause a range of adverse reactions, from mild to serious.

Common Side Effects

  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Nausea: mild to moderate upset stomach.
  • Headache: persistent or intermittent pain.
  • Fatigue: increased tiredness or lack of energy.
  • Blurred vision: temporary visual disturbances.
  • Diplopia: double vision in some patients.

Serious or Rare Side Effects

  • Suicidal thoughts: emergence of depressive symptoms or suicidal ideation.
  • Severe rash: including Stevens‑Johnson syndrome.
  • Cardiac arrhythmia: especially PR‑interval prolongation.
  • Respiratory depression: marked slowing of breathing.
  • Anaphylaxis: acute allergic reaction with hives, swelling, or difficulty breathing.
  • Hepatotoxicity: signs of liver injury such as jaundice.

Precautions & Warnings

Before initiating Lacosamide, clinicians should evaluate several safety considerations.

  • Renal impairment: adjust dose in patients with reduced kidney function.
  • Hepatic impairment: monitor liver enzymes and consider dose modification.
  • Cardiac conduction: obtain baseline ECG; avoid in patients with significant PR‑interval prolongation.
  • Pregnancy: use only if potential benefit justifies potential risk; data are limited.
  • Concomitant CNS depressants: monitor for enhanced sedation or respiratory effects.
  • Store at ambient temperature: keep below 25 °C, in the original packaging, protected from moisture and direct sunlight.

Avoid Interactions

Lacosamide can interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase lacosamide plasma levels.
  • Strong CYP3A4 inducers (e.g., carbamazepine): may reduce efficacy.
  • Other sodium‑channel blockers (e.g., phenytoin): risk of additive cardiac effects.

Moderate Interactions (Monitor Closely)

  • Opioids: potential for enhanced CNS depression.
  • Alcohol: may increase dizziness and sedation.
  • Anticoagulants (e.g., warfarin): monitor INR for possible changes.
  • Antidepressants (e.g., SSRIs): watch for mood alterations.
  • Diuretics: may affect electrolyte balance influencing cardiac conduction.

Frequently Asked Questions

Lacosamide Krka is prescribed as an adjunctive therapy for the treatment of partial‑onset seizures and for patients with refractory epilepsy. It helps reduce the frequency and severity of seizures when added to other antiepileptic regimens.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes. This action stabilizes hyper‑excitable neurons, limits repetitive firing, and thereby diminishes the propagation of seizure activity without markedly affecting normal neuronal signaling.

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

Safety data for lacosamide in pregnancy and lactation are limited. It should only be used if the potential therapeutic benefit justifies any potential risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To place an order, 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.

Lacosamide’s unique mechanism—enhancing slow sodium‑channel inactivation—differs from many traditional antiepileptics that target fast inactivation. This can provide additional seizure control in patients who have not responded adequately to other agents, while offering a distinct side‑effect profile.

Lacosamide Krka tablets should be stored at ambient temperature, below 25 °C, in the original container to protect from moisture and light. Keep the product out of reach of children and do not use after the expiry date.

Lacosamide Krka is taken orally, usually as a tablet, with or without food. The exact administration schedule—once or twice daily—depends on the prescriber’s dosing plan and patient tolerance.

Serious risks include the potential for suicidal thoughts or behavior, severe skin reactions such as Stevens‑Johnson syndrome, cardiac conduction abnormalities like PR‑interval prolongation, and rare cases of respiratory depression or anaphylaxis. Prompt medical attention is required if any of these occur.

Patients with known hypersensitivity to lacosamide or any excipients, those with significant cardiac conduction disorders (e.g., marked PR‑interval prolongation), and individuals taking contraindicated strong CYP3A4 inhibitors or inducers should avoid using Lacosamide Krka unless a specialist advises otherwise.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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