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 an anti‑epileptic drug presented as an oral tablet for oral use. It is indicated for the treatment of partial‑onset (focal) seizures in adults and children, helping to reduce seizure frequency and improve quality of life.

GNH India supplies Lacosamide Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality assurance protocols and regulatory standards to ensure product integrity throughout the global distribution chain.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

  • Lacosamide is an anti‑epileptic medication used to manage seizure disorders.
  • Partial‑onset seizures: reduces seizure frequency in patients with focal epilepsy.
  • Focal seizures: provides adjunctive control when monotherapy is insufficient.
  • Adjunct therapy for epilepsy: used as an add‑on treatment in combination with other antiepileptic drugs.
  • Refractory epilepsy: offers an alternative mechanism for patients not responding to other agents.

How It Works

  • Lacosamide selectively enhances the slow inactivation of voltage‑gated sodium channels, stabilizing neuronal membranes and reducing hyper‑excitability. It also binds to collapsin response mediator protein‑2 (CRMP2), modulating neuronal differentiation and axonal transport. By preferentially targeting the non‑active state of the channel, Lacosamide does not significantly affect normal neuronal firing, which helps maintain physiological function while preventing pathological bursts.

Side Effects

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

Common Side Effects

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

Serious or Rare Side Effects

  • Cardiac arrhythmia: irregular heart rhythm, including PR‑interval prolongation.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Suicidal thoughts: emergence of depressive symptoms or suicidal ideation.

Precautions & Warnings

When prescribing Lacosamide, clinicians should consider several safety considerations.

  • Cardiac monitoring: assess ECG for PR‑interval changes before and during therapy.
  • Renal impairment: adjust dose in patients with reduced kidney function.
  • Concomitant CNS depressants: avoid excessive sedation when combined with alcohol or opioids.
  • Pregnancy: use only if potential benefit justifies potential risk, as safety data are limited.
  • Driving and machinery: caution patients about possible dizziness affecting ability to operate vehicles.
  • Store at ambient temperature: keep below 25 °C, protect from moisture and keep in original container.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., carbamazepine, phenytoin): may reduce Lacosamide plasma levels.
  • Class III anti‑arrhythmic agents (e.g., amiodarone): may increase risk of cardiac conduction abnormalities.

Moderate Interactions (Monitor Closely)

  • Opioids (e.g., tramadol, oxycodone): may enhance central nervous system depression.
  • Alcohol: concurrent use can increase dizziness and sedation.
  • Other antiepileptic drugs (e.g., valproate, levetiracetam): may require dose adjustments based on therapeutic response.

Frequently Asked Questions

Lacosamide Stada is an anti‑epileptic medication indicated for the treatment of partial‑onset (focal) seizures in patients with epilepsy, helping to reduce seizure frequency and improve overall seizure control.

Lacosamide works by enhancing the slow inactivation of voltage‑gated sodium channels and binding to CRMP2, which stabilizes neuronal membranes, decreases hyper‑excitability, and limits the spread of epileptic discharges.

The dosage of Lacosamide is individualized; the prescribing clinician determines the appropriate starting dose and titration schedule based on the patient’s age, renal function, and therapeutic response.

Safety data for Lacosamide in pregnancy are limited; it should be used only when the potential benefit outweighs the potential risk. Breastfeeding decisions should consider the drug’s presence in milk and the infant’s benefit.

To order, submit an enquiry on the product page at gnhindia.com specifying 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 necessary import documentation.

Compared with many traditional antiepileptics, Lacosamide has a distinct mechanism targeting slow sodium‑channel inactivation and CRMP2, which may offer efficacy in patients who have not responded adequately to other agents, while presenting a different side‑effect profile.

Store the tablets at ambient temperature below 25 °C, in the original packaging, protected from moisture and light. Keep out of reach of children and do not use if the package is damaged.

Lacosamide is taken orally, usually as a tablet, with or without food. The exact dosing schedule and titration are set by the prescriber to achieve optimal seizure control.

Serious risks include cardiac arrhythmias such as PR‑interval prolongation, severe skin reactions like Stevens‑Johnson syndrome, and emergence of suicidal thoughts or depressive symptoms; patients should be monitored for these events.

Lacosamide is contraindicated in patients with known hypersensitivity to the drug and should be used with caution or avoided in individuals with significant cardiac conduction disorders, severe renal impairment, or those taking interacting medications that cannot be managed.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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