Product image of Lacosamida Teva (Lacosamide) supplied by GNH India

Lacosamida Teva

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamida Teva (Lacosamide)

Lacosamide, the active ingredient in Lacosamida Teva, is a sodium channel blocker presented as an oral formulation for oral use. It is indicated as adjunctive therapy for partial‑onset seizures in patients with epilepsy.
GNH India supplies Lacosamida Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Lacosamida Teva is a sodium channel‑blocking antiepileptic used to manage focal seizure disorders.

  • Partial‑onset seizures (focal seizures): Adjunctive therapy to reduce seizure frequency in epilepsy patients.
  • Focal epilepsy: Improves overall seizure control when added to existing antiepileptic regimens.
  • Refractory focal seizures: Provides additional seizure reduction for patients not adequately controlled by monotherapy.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, which stabilises hyper‑excitable neuronal membranes and diminishes repetitive neuronal firing. This selective modulation reduces the propagation of epileptic discharges without markedly affecting normal neuronal activity.

Side Effects

Lacosamida Teva may cause a range of adverse reactions, some of which are more frequent than others.

Common Side Effects

  • Dizziness: Transient sensation of light‑headedness or imbalance.
  • Headache: Mild to moderate pain in the head region.
  • Nausea: Stomach upset often occurring after dosing.
  • Fatigue: Generalised tiredness or reduced energy.
  • Diplopia: Temporary double vision.
  • Somnolence: Increased sleepiness during the day.

Serious or Rare Side Effects

  • Cardiac arrhythmia: Irregular heart rhythm requiring medical attention.
  • Suicidal ideation: Thoughts of self‑harm that should be reported immediately.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Cardiac conduction abnormalities: PR‑interval prolongation on ECG.
  • Hypersensitivity reactions: Anaphylaxis or severe allergic response.
  • Hepatic dysfunction: Elevated liver enzymes or liver injury.

Precautions & Warnings

Before initiating therapy, several safety considerations should be reviewed.

  • Renal impairment: Assess kidney function and adjust dosing if necessary.
  • Hepatic impairment: Monitor liver enzymes and consider dose modification.
  • Concomitant antiepileptics: Watch for additive central nervous system effects.
  • Pregnancy: Use only if the potential benefit justifies the potential risk to the fetus.
  • Driving and operating machinery: Caution advised due to possible dizziness or somnolence.
  • Store at ambient temperature: Keep below 25°C, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): May increase lacosamide plasma levels.
  • Carbamazepine: May reduce lacosamide effectiveness.
  • Other sodium channel blockers (e.g., phenytoin): Heightened risk of central nervous system depression.

Moderate Interactions (Monitor Closely)

  • Additional antiepileptics (e.g., valproate): Monitor for additive side effects.
  • Alcohol: May potentiate sedation and dizziness.
  • Antihypertensives: Observe blood pressure for possible additive lowering effect.

Frequently Asked Questions

Lacosamida Teva contains lacosamide, an antiepileptic indicated as adjunctive therapy for partial‑onset (focal) seizures in patients with epilepsy. It is prescribed when seizure control is insufficient with existing medication regimens.

Lacosamide selectively enhances the slow inactivation of voltage‑gated sodium channels in neurons. This stabilises hyper‑excitable membranes, reduces repetitive firing, and limits the spread of epileptic activity without markedly affecting normal neuronal signalling.

The dosage of Lacosamida Teva is determined individually by a qualified prescriber based on the patient’s clinical condition, response, and tolerability. Specific dosing regimens should be obtained from the treating healthcare professional.

Safety data for lacosamide in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and under close medical supervision.

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 necessary import documentation.

Lacosamide is a sodium‑channel blocker with a unique mechanism that enhances slow inactivation, differing from many older agents that target fast inactivation. This can offer complementary seizure control when combined with other antiepileptics, often with a distinct side‑effect profile.

Lacosamida Teva should be stored at ambient temperature, preferably below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and avoid exposing it to extreme temperatures.

The medication is taken orally, usually as a tablet, and should be swallowed with water. It can be taken with or without food, but consistency with respect to meals helps maintain stable drug levels. Follow the prescriber’s instructions for timing and frequency.

Serious adverse events include cardiac arrhythmias, PR‑interval prolongation, severe skin reactions such as Stevens‑Johnson syndrome, and suicidal thoughts or behaviours. Patients should be monitored for any new cardiac symptoms, skin changes, or mood alterations and seek immediate medical attention if they occur.

Patients with known hypersensitivity to lacosamide or any component of the formulation should avoid the product. Caution is also advised for individuals with significant cardiac conduction disorders, severe hepatic impairment, or those taking interacting medications that could increase toxicity.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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