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

Lacosamide Accord

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamide Accord (Lacosamide)

Lacosamide, the active ingredient in Lacosamide Accord, is a sodium channel blocker presented as an oral formulation for oral use. It treats partial‑onset seizures in patients with epilepsy.

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

Manufacturer / TM Owner

Accord-Uk Limited

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Indications & Clinical Uses

Lacosamide is an antiepileptic medication that modulates neuronal sodium channels.

  • Partial‑onset seizures: reduces seizure frequency in patients with focal epilepsy.
  • Epilepsy: provides adjunctive therapy to improve overall seizure control.
  • Refractory focal epilepsy: helps achieve better seizure management when other treatments are insufficient.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes, stabilizing hyperexcitable neuronal membranes and decreasing repetitive firing. This modulation reduces neuronal hyperexcitability that underlies seizure generation, contributing to its antiepileptic effect.

Side Effects

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

Common Side Effects

  • Dizziness: sensation of light‑headedness or imbalance.
  • Nausea: upset stomach often accompanied by an urge to vomit.
  • Headache: mild to moderate pain in the head region.
  • Fatigue: feeling unusually tired or lacking energy.
  • Blurred vision: temporary loss of visual clarity.
  • Diplopia: double vision, especially at higher doses.

Serious or Rare Side Effects

  • Stevens‑Johnson syndrome: severe skin reaction requiring immediate medical attention.
  • Cardiac arrhythmias: irregular heart rhythms, particularly in patients with pre‑existing conduction disorders.
  • Suicidal thoughts: emergence of depressive symptoms or suicidal ideation.
  • Severe hepatic injury: marked elevation of liver enzymes or liver failure.
  • Life‑threatening skin reactions: toxic epidermal necrolysis or drug reaction with eosinophilia and systemic symptoms (DRESS).

Precautions & Warnings

When prescribing Lacosamide, clinicians should consider several safety aspects.

  • Renal impairment: assess kidney function and adjust dose if necessary.
  • Hepatic impairment: monitor liver enzymes and consider dose modification.
  • Cardiac conduction disorders: use caution in patients with known arrhythmias or AV‑node disease.
  • Pregnancy: risk category is unknown; discuss potential benefits and risks with the patient.
  • Concomitant antiepileptics: monitor for additive CNS effects and possible pharmacokinetic interactions.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, and protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Carbamazepine: may lower lacosamide plasma concentrations, reducing effectiveness.
  • Strong CYP2C19 inhibitors (e.g., fluconazole): can increase lacosamide exposure, raising toxicity risk.
  • Other sodium‑channel blockers (e.g., phenytoin): may enhance cardiac conduction effects.

Moderate Interactions (Monitor Closely)

  • Valproate: combined use may increase CNS side‑effects; monitor patient tolerance.
  • Alcohol: concurrent consumption can intensify dizziness and sedation.
  • Other antiepileptics: additive side‑effects may require dose adjustments.

Frequently Asked Questions

Lacosamide Accord contains the active ingredient lacosamide, an antiepileptic drug indicated for the treatment of partial‑onset seizures in patients with epilepsy. It is used as an adjunctive therapy to help reduce seizure frequency when other medications are insufficient.

Lacosamide works by enhancing the slow inactivation of voltage‑gated sodium channels in neurons. This stabilizes hyper‑excitable neuronal membranes, decreasing repetitive firing and thereby reducing the likelihood of seizure activity.

The specific dose of Lacosamide Accord is determined by the prescribing clinician based on the patient’s age, weight, renal and hepatic function, and overall treatment plan. No fixed regimen is provided here; the prescriber sets the appropriate dosage.

The safety of lacosamide in pregnancy and lactation has not been definitively established. Healthcare providers should weigh the potential benefits against possible risks and discuss these considerations with the patient before initiating therapy.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies, and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details, and necessary import documentation.

Lacosamide belongs to the sodium‑channel blocker class and offers a distinct mechanism by enhancing slow inactivation, unlike many older agents that affect fast inactivation. This can provide better seizure control for some patients, especially when combined with other antiepileptics that have different mechanisms.

Lacosamide Accord should be stored at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture, and avoid exposure to direct sunlight to maintain stability.

Lacosamide Accord is administered orally, typically as a tablet or oral solution, and should be taken according to the prescriber’s instructions. It can be taken with or without food, but consistency with meals may help reduce gastrointestinal discomfort.

Serious risks include severe skin reactions such as Stevens‑Johnson syndrome, cardiac arrhythmias especially in patients with pre‑existing conduction disorders, and the emergence of suicidal thoughts or behaviors. Patients should seek immediate medical attention if any of these occur.

Lacosamide Accord is contraindicated in patients with known hypersensitivity to lacosamide or any of its excipients. Caution is also advised for individuals with significant cardiac conduction abnormalities, severe renal or hepatic impairment, and those taking interacting medications that may increase toxicity.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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