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

Lacosamide Zentiva

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamide Zentiva (Lacosamide)

Lacosamide, the active ingredient in Lacosamide Zentiva, is a sodium channel blocker presented as an oral tablet for oral use. It is employed to treat partial‑onset seizures in patients with epilepsy and may be used as adjunct therapy when seizures are not adequately controlled by other antiepileptic agents.

GNH India supplies Lacosamide Zentiva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company ensures product quality through stringent quality‑assurance processes and provides regulatory support for global distribution.

Manufacturer / TM Owner

Zentiva, K.S.

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Indications & Clinical Uses

Lacosamide is indicated for seizure disorders that involve abnormal neuronal firing in the central nervous system.

  • Partial-onset seizures: reduces seizure frequency and severity in patients with focal epilepsy.
  • Adjunct therapy for refractory epilepsy: used alongside other antiepileptic drugs when monotherapy is insufficient.
  • Epilepsy (focal onset): helps achieve better seizure control in individuals diagnosed with focal onset epilepsy.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes, stabilizing hyperexcitable neuronal membranes and decreasing repetitive firing. By selectively targeting the late phase of sodium channel activity, it reduces neuronal hyperexcitability without significantly affecting normal conduction, thereby contributing to seizure control. The drug’s action is independent of the fast inactivation process, allowing it to complement other sodium‑channel blockers and provide additive antiepileptic effects.

Side Effects

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

Common Side Effects

  • Dizziness: sensation of lightheadedness or imbalance.
  • Nausea: feeling of stomach upset or urge to vomit.
  • Headache: mild to moderate cranial pain.
  • Fatigue: unusual tiredness or lack of energy.
  • Blurred vision: temporary visual disturbances.
  • Diplopia: double vision episodes.

Serious or Rare Side Effects

  • Stevens‑Johnson syndrome: severe skin reaction with blistering.
  • Cardiac arrhythmia: alterations in heart rhythm, including PR‑interval prolongation.
  • Suicidal ideation: thoughts of self‑harm requiring immediate evaluation.
  • Severe hypersensitivity: rash, fever, and organ involvement.
  • Rhabdomyolysis: muscle breakdown leading to elevated creatine kinase.
  • Anaphylaxis: acute, life‑threatening allergic reaction.

Precautions & Warnings

When prescribing Lacosamide, clinicians should consider several precautionary measures to ensure patient safety.

  • Renal impairment: assess kidney function and adjust therapy if necessary.
  • Cardiac monitoring: evaluate baseline ECG as Lacosamide can prolong PR interval.
  • Pregnancy: safety data are limited; weigh potential benefits against risks.
  • Concomitant antiepileptics: review for possible additive CNS effects.
  • Discontinuation: avoid abrupt cessation to prevent seizure worsening.
  • Store at ambient temperature: keep below 25 °C in original packaging, protect from moisture.

Avoid Interactions

Lacosamide can interact with other medicines, influencing its plasma levels or cardiac effects.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors: may increase Lacosamide concentrations, raising toxicity risk.
  • Other sodium‑channel blockers: combined use can enhance cardiac conduction abnormalities.
  • Drugs that prolong PR interval (e.g., beta‑blockers): may lead to significant heart‑rate slowing.

Moderate Interactions (Monitor Closely)

  • Carbamazepine: may reduce Lacosamide levels, decreasing efficacy.
  • Phenytoin: can lower Lacosamide plasma concentrations.
  • Alcohol: may intensify central nervous system depression.
  • Anticoagulants: monitor for altered bleeding risk when used together.

Frequently Asked Questions

Lacosamide Zentiva is prescribed to treat partial‑onset seizures in patients with focal epilepsy. It may be used as monotherapy or added to other antiepileptic drugs when seizure control is not achieved with a single agent.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neurons, stabilising hyper‑excitable membranes and reducing repetitive firing. This selective action lowers neuronal hyperexcitability, helping to prevent seizure activity.

The dose is individually determined by the prescribing clinician based on the patient’s age, renal function, seizure frequency, and response to therapy. No fixed regimen is provided here; the prescriber will set the appropriate dosage.

Safety data for Lacosamide in pregnancy and lactation are limited. The drug should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and decisions should be made in consultation with a healthcare professional.

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 any necessary import documentation.

Lacosamide’s unique mechanism—enhancing slow sodium‑channel inactivation—differs from many traditional antiepileptics that target fast inactivation. This can provide additive seizure control when combined with other agents, and it generally has a favourable tolerability profile compared with some older sodium‑channel blockers.

Store the tablets at ambient temperature, preferably below 25 °C. Keep them in the original container, protect from moisture and direct sunlight, and ensure the packaging remains tightly closed until use.

Lacosamide Zentiva is taken orally as a tablet. The tablet should be swallowed whole with water and can be taken with or without food, following the dosing schedule prescribed by the treating physician.

Serious risks include severe skin reactions such as Stevens‑Johnson syndrome, cardiac conduction abnormalities like PR‑interval prolongation, suicidal thoughts or behaviors, and rare hypersensitivity reactions such as anaphylaxis. Any of these symptoms require immediate medical attention.

Patients with known hypersensitivity to lacosamide or any of its excipients should avoid the product. Caution is also advised for individuals with significant cardiac conduction disorders, uncontrolled renal impairment, or those taking medications that strongly interact with lacosamide without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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