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

Lacosamide Stada

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamide Stada (Lacosamide)

Lacosamide, the active ingredient in Lacosamide Stada, is a sodium channel modifier presented as an oral tablet for oral use. It is employed as adjunctive therapy for partial‑onset seizures in patients with epilepsy, helping to reduce seizure frequency when added to existing antiepileptic regimens. The drug enhances the slow inactivation of voltage‑gated sodium channels, stabilizing hyper‑excitable neuronal membranes.

GNH India supplies Lacosamide Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. Its distribution complies with European Union quality standards and is intended for use in regulated healthcare settings.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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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: provides adjunctive seizure control when added to existing antiepileptic therapy in patients with epilepsy.
  • Focal seizures: helps reduce the frequency of focal seizure episodes as part of combination treatment.
  • Epilepsy with refractory partial seizures: offers an additional therapeutic option for patients whose seizures are not adequately controlled by other antiepileptic drugs.

How It Works

  • Lacosamide selectively enhances the slow inactivation phase of voltage‑gated sodium channels in neuronal membranes. By stabilizing the inactive state of these channels, it reduces the ability of neurons to fire repetitively, thereby diminishing hyper‑excitability that underlies seizure generation. This targeted modulation does not significantly affect normal neuronal conduction, allowing seizure control with a relatively specific mechanism.

Side Effects

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

Common Side Effects

  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Nausea: feeling of stomach upset or urge to vomit.
  • Headache: mild to moderate cranial pain.
  • Fatigue: unusual tiredness or lack of energy.

Serious or Rare Side Effects

  • Cardiac conduction abnormalities: such as PR‑interval prolongation or atrioventricular block.
  • Severe skin reactions: including Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Suicidal thoughts or behavior: emergence of depressive symptoms or suicidal ideation.

Precautions & Warnings

When prescribing lacosamide, clinicians should consider several safety aspects.

  • Renal impairment: adjust therapy and monitor renal function.
  • Hepatic impairment: use with caution and assess liver enzymes.
  • Cardiac conduction disorders: avoid in patients with known PR‑interval prolongation.
  • Pregnancy: safety not established; weigh benefits against potential risks.
  • Suicidal ideation: monitor patients for mood changes and depressive symptoms.
  • Store below 25°C: keep in the original packaging, protect from moisture and heat.

Avoid Interactions

Lacosamide can interact with other medicines, requiring attention to potential effects.

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • Alcohol: may enhance central nervous system depression.
  • Antihypertensive agents: additive blood pressure‑lowering effect.
  • Other antiepileptic drugs: may require dose adjustments based on therapeutic response.

Frequently Asked Questions

Lacosamide Stada is indicated as an adjunctive treatment for partial‑onset seizures in patients with epilepsy. It is added to existing antiepileptic regimens to help lower seizure frequency when monotherapy does not provide adequate control.

Lacosamide selectively enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes. This stabilizes the inactive state of the channels, reducing repetitive neuronal firing and thereby diminishing the hyper‑excitability that contributes to seizure generation.

The dosing regimen for lacosamide is individualized and must be determined by a qualified prescriber based on the patient’s clinical condition, response to therapy, and any relevant comorbidities. No specific dose is provided here.

Safety data for lacosamide during pregnancy and lactation are limited, and the pregnancy category is listed as unknown. Clinicians should weigh potential benefits against possible risks and consider alternative therapies when appropriate.

To place an order, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies 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 mechanism—enhancing slow sodium‑channel inactivation—is distinct from many older antiepileptics that block fast sodium channels. This unique profile can offer efficacy in patients who have not responded to other agents, while its side‑effect spectrum may differ, often showing fewer cognitive effects but a potential for cardiac conduction changes.

Lacosamide Stada should be stored at temperatures below 25 °C, in its original packaging, protected from moisture and direct heat. Keep the product out of reach of children and avoid exposure to excessive humidity.

The medication is supplied as an oral tablet and is taken by mouth. It is usually administered with or without food, according to the prescriber’s instructions, and should be swallowed whole with a glass of water.

Serious risks include cardiac conduction abnormalities such as PR‑interval prolongation or atrioventricular block, severe skin reactions like Stevens‑Johnson syndrome, and the emergence of suicidal thoughts or behavior. Patients should be monitored closely for these events, especially during treatment initiation and dose changes.

Lacosamide is contraindicated in patients with known severe cardiac conduction disorders, such as advanced atrioventricular block, and in individuals who have demonstrated hypersensitivity to the drug or any of its excipients. Caution is also advised for patients with significant renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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