Product image of Lacosamid Zentiva (Lacosamide) supplied by GNH India

Lacosamid Zentiva

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamid Zentiva (Lacosamide)

Lacosamide, the active ingredient in Lacosamid Zentiva, is an anticonvulsant presented as an oral tablet for oral use. It is used as adjunctive therapy in patients with partial‑onset seizures and primary generalized tonic‑clonic seizures.

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

Manufacturer / TM Owner

Zentiva, K.S.

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Indications & Clinical Uses

Lacosamide is an anticonvulsant that acts on neuronal sodium channels to control seizure activity.

  • Partial‑onset seizures: reduces seizure frequency when added to existing therapy.
  • Primary generalized tonic‑clonic seizures: provides adjunctive seizure control in combination with other antiepileptics.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, stabilizing hyper‑excitable neuronal membranes and limiting repetitive firing. The drug binds to the intracellular domain of the channel, shifting the equilibrium toward the inactivated state. This action diminishes the ability of neurons to fire high‑frequency action potentials that underlie epileptic discharges, providing therapeutic benefit in focal and generalized seizure types.

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: mild to moderate stomach upset.
  • Headache: intermittent or persistent pain.
  • Fatigue: feeling unusually tired.
  • Diplopia: double vision.
  • Tremor: mild shaking of limbs.

Serious or Rare Side Effects

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

Precautions & Warnings

When prescribing Lacosamid Zentiva, clinicians should consider several safety measures.

  • Cardiac monitoring: assess ECG for PR interval prolongation, especially in patients with cardiac disease.
  • Renal impairment: adjust dose in patients with severe renal dysfunction.
  • Hepatic impairment: use caution and consider dose reduction in liver disease.
  • Pregnancy: avoid use unless benefits outweigh potential risks, as safety data are limited.
  • Discontinuation: do not stop abruptly; taper to reduce seizure recurrence risk.
  • Store at below 25°C: keep in original packaging, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inducers: may reduce lacosamide plasma levels, decreasing effectiveness.
  • Concomitant sodium channel blockers (e.g., carbamazepine, phenytoin): increase risk of cardiac conduction abnormalities.
  • Dual antiplatelet therapy: heightened bleeding risk when combined with anticoagulants.

Moderate Interactions (Monitor Closely)

  • Hormonal contraceptives: may lower contraceptive efficacy, requiring additional methods.
  • Antidepressants (e.g., SSRIs): monitor for increased risk of suicidal thoughts.
  • Diuretics: watch for electrolyte disturbances that could affect cardiac rhythm.

Frequently Asked Questions

Lacosamid Zentiva contains lacosamide, an anticonvulsant indicated as adjunctive therapy for partial‑onset seizures and primary generalized tonic‑clonic seizures in patients with epilepsy.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, stabilizing hyper‑excitable neuronal membranes and reducing the ability of neurons to fire high‑frequency action potentials that generate seizures.

The dosage of Lacosamid Zentiva is individualized; the prescribing clinician determines the appropriate dose and titration schedule based on the patient’s clinical condition and response.

Safety data in pregnancy and lactation are limited; the product should be used only if the potential benefit justifies the potential risk to the fetus or infant, and clinicians should discuss uncertainties with the patient.

To request Lacosamid Zentiva, 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.

Compared with other sodium‑channel blockers, lacosamide selectively enhances slow inactivation, which may offer a different side‑effect profile and lower risk of certain cardiac effects, while providing comparable seizure control as adjunctive therapy.

Lacosamid Zentiva should be stored at temperatures below 25 °C in its original packaging, protected from moisture and light, and kept out of reach of children.

The medication is taken orally, usually as a tablet, and should be swallowed with water. It may be taken with or without food, according to the prescribing information.

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

Lacosamid Zentiva is contraindicated in patients with known hypersensitivity to lacosamide or any of its excipients, and it should be used with caution or avoided in individuals with significant cardiac conduction disorders or uncontrolled severe renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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