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

Lacosamide Olpha

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamide Olpha (Lacosamide)

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

Manufacturer / TM Owner

Olpha As

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Indications & Clinical Uses

Lacosamide is an antiepileptic drug indicated for seizure disorders and is used as an add‑on therapy in epilepsy management.

  • Partial‑onset seizures: reduces seizure frequency when added to existing antiepileptic regimens.
  • Primary generalized tonic‑clonic seizures: used as adjunctive treatment to improve overall seizure control.
  • Focal epilepsy: helps achieve better control of focal seizure activity.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, stabilizing neuronal membranes and reducing hyperexcitability. It also binds to the collapsin response mediator protein‑2 (CRMP2), modulating neuronal signaling pathways involved in seizure propagation.

Side Effects

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

Common Side Effects

  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Nausea: feeling of stomach upset or urge to vomit.
  • Fatigue: persistent tiredness or lack of energy.
  • Headache: mild to moderate cranial pain.
  • Blurred vision: temporary visual disturbances.
  • Somnolence: increased sleepiness during the day.

Serious or Rare Side Effects

  • Cardiac conduction abnormalities: PR interval prolongation that may lead to arrhythmia.
  • Suicidal ideation: emergence of thoughts of self‑harm.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hypersensitivity: rash, swelling, or anaphylactic responses.
  • Elevated liver enzymes: indicating potential hepatic stress.

Precautions & Warnings

When prescribing Lacosamide, clinicians should consider several safety aspects.

  • Renal impairment: dose adjustment may be required based on renal function.
  • Hepatic impairment: monitor liver function tests and adjust dosing if needed.
  • Cardiac conduction: obtain baseline ECG and monitor for PR interval changes.
  • Pregnancy: risk category unknown; use only if benefits outweigh potential risks.
  • Concomitant CNS depressants: may increase sedation and respiratory depression.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Lacosamide can interact with other medicines, influencing its efficacy and safety. Major Interactions (Avoid):\n- Class I antiarrhythmics: may exacerbate PR interval prolongation.

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): increase lacosamide plasma concentrations.
  • Strong CYP3A4 inducers (e.g., carbamazepine): reduce lacosamide levels, diminishing effectiveness.

Moderate Interactions (Monitor Closely)

  • Other antiepileptic drugs: may require dose adjustments to maintain seizure control.
  • Alcohol: additive central nervous system depression, increasing drowsiness.
  • Tramadol: may raise the risk of seizures when used together.

Frequently Asked Questions

Lacosamide Olpha is used as an adjunctive treatment for patients with epilepsy, specifically to reduce the frequency of partial‑onset seizures when added to existing antiepileptic therapy.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels and binds to CRMP2 protein, which together stabilize neuronal membranes and decrease abnormal neuronal firing that leads to seizures.

The prescribed dose of Lacosamide Olpha is determined by the treating physician based on individual patient factors, seizure type, and response to therapy. No fixed regimen is provided here.

The safety of Lacosamide in pregnancy and lactation has not been fully established. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and under close medical supervision.

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 necessary import documentation.

Lacosamide’s unique mechanism—enhancing slow sodium‑channel inactivation—differs from many traditional antiepileptics that target fast inactivation. This can provide complementary seizure control when combined with other agents, though individual response varies.

Lacosamide Olpha should be stored at temperatures below 25 °C, in its original container, protected from moisture and direct sunlight. No refrigeration is required for this oral formulation.

Lacosamide Olpha is taken orally, usually as a tablet, and should be swallowed with water. The exact timing and frequency are set by the prescribing clinician.

Serious risks include cardiac conduction abnormalities such as PR‑interval prolongation, potential suicidal thoughts, severe skin reactions like Stevens‑Johnson syndrome, and hypersensitivity reactions that may require immediate medical attention.

Patients with known hypersensitivity to lacosamide or any component of the formulation, those with uncontrolled cardiac conduction disorders, and individuals for whom the prescriber determines the risks outweigh the benefits should avoid using Lacosamide Olpha.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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