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 an Anticonvulsant presented as an oral tablet for oral use. It is indicated for the treatment of partial‑onset seizures, either as monotherapy or adjunctive therapy in patients with epilepsy.

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 acts on neuronal sodium channels to control seizure activity.

  • Partial‑onset seizures: reduces the frequency and severity of focal seizures.
  • Adjunctive therapy for epilepsy: improves overall seizure control when added to other antiepileptic medications.
  • Focal seizures: helps achieve better seizure freedom in patients with focal onset epilepsy.

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 propagation of epileptiform activity without significantly affecting normal neuronal function.

Side Effects

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

Common Side Effects

  • Dizziness: sensation of lightheadedness or unsteadiness.
  • Nausea: mild to moderate stomach upset.
  • Fatigue: increased tiredness or lack of energy.
  • Headache: mild to moderate pain in the head.
  • Blurred vision: temporary visual disturbances.
  • Diplopia: double vision in some patients.

Serious or Rare Side Effects

  • Suicidal thoughts or behavior: new or worsening mood changes.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Cardiac arrhythmias: including PR‑interval prolongation.
  • Respiratory depression: especially when combined with other CNS depressants.
  • Allergic reactions: anaphylaxis or angioedema.
  • Hepatotoxicity: signs of liver injury such as jaundice.

Precautions & Warnings

Before initiating therapy with Lacosamide, consider the following precautions.

  • Renal impairment: dose adjustment may be required in patients with reduced kidney function.
  • Hepatic impairment: monitor liver enzymes and adjust dosing as needed.
  • Concomitant CNS depressants: increased risk of sedation and respiratory depression.
  • Cardiac conduction disorders: avoid in patients with known PR‑interval prolongation.
  • Pregnancy: safety not established; weigh benefits against potential risks.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lacosamide can interact with several medications; awareness of interaction severity guides clinical decisions.

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • Alcohol: additive CNS depression may increase dizziness and sedation.
  • Hormonal contraceptives: lacosamide may reduce contraceptive efficacy; advise alternative methods.
  • CYP2C19 inhibitors (e.g., fluoxetine, omeprazole): may modestly increase lacosamide exposure.
  • Other antiepileptics (e.g., valproate): monitor for enhanced side‑effect profile.
  • Anticoagulants: observe for any changes in bleeding risk, though data are limited.

Frequently Asked Questions

Lacosamide Krka is prescribed to treat partial‑onset (focal) seizures in patients with epilepsy. It can be used alone or added to other antiepileptic drugs to improve seizure control when monotherapy is insufficient.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neurons, stabilizing hyper‑excitable membranes and reducing repetitive firing. This action limits the spread of epileptiform activity without markedly affecting normal neuronal signaling.

The appropriate 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. The drug should only be used if the potential benefit justifies any potential risk to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss risks with their healthcare provider.

To order Lacosamide Krka, 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 for patients who have not responded adequately to other agents, while offering a generally favorable tolerability profile.

Lacosamide Krka should be stored at room temperature, below 25 °C, in its original packaging. Protect the product from moisture, excessive heat, and direct sunlight to maintain its stability and potency.

Lacosamide Krka is administered orally, typically as a tablet taken with or without food. The exact administration schedule, including timing and any dose titration, is directed by the prescribing clinician.

Serious risks include the potential for suicidal thoughts or behavior, severe skin reactions such as Stevens‑Johnson syndrome, cardiac conduction abnormalities (e.g., PR‑interval prolongation), and respiratory depression, especially when combined with other central nervous system depressants.

Patients with known hypersensitivity to lacosamide or any of its excipients should avoid the product. Additionally, individuals with significant cardiac conduction disorders, uncontrolled severe hepatic or renal impairment, or those taking contraindicated medications should not use lacosamide without close medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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