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

Lacosamidă Teva

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamidă Teva (Lacosamide)

Lacosamide, the active ingredient in Lacosamidă Teva, is an anticonvulsant presented as an oral tablet for oral use. It is indicated for the treatment of partial‑onset seizures and is used as adjunctive therapy in patients with epilepsy.
GNH India supplies Lacosamidă Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva Pharmaceuticals S.R.L

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Indications & Clinical Uses

Lacosamide is an anticonvulsant that targets seizure activity in the central nervous system.

  • Partial‑onset seizures: reduces the frequency of focal seizures when added to existing therapy.
  • Adjunctive therapy for epilepsy: improves overall seizure control as part of combination treatment.
  • Focal seizures: helps achieve better seizure management in patients with focal onset epilepsy.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes, stabilizing hyper‑excitable neuronal membranes and decreasing repetitive neuronal firing. This modulation reduces the propagation of epileptic discharges without significantly affecting normal neuronal activity.

Side Effects

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

Common Side Effects

  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Nausea: mild to moderate stomach upset.
  • Fatigue: feeling unusually tired or weak.
  • Headache: mild to moderate cranial pain.
  • Diplopia: transient double vision.
  • Tremor: fine shaking of the hands or limbs.

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 ideation: thoughts of self‑harm or suicide.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Acute pancreatitis: inflammation of the pancreas.
  • Anaphylaxis: severe allergic reaction with breathing difficulty.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient history and monitor for specific risks.

  • Renal impairment: adjust monitoring as drug is renally excreted.
  • Hepatic dysfunction: assess liver function tests regularly.
  • Cardiac conduction disorders: obtain baseline ECG and monitor PR interval.
  • Pregnancy and lactation: use only if potential benefit outweighs risk, as safety data are limited.
  • Store at ambient temperature: keep below 25°C in the original container, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., carbamazepine, phenytoin): may reduce lacosamide plasma levels.
  • Concomitant use with other sodium‑channel blockers (e.g., lamotrigine) at high doses: increased risk of cardiac conduction effects.

Moderate Interactions (Monitor Closely)

  • CYP2C19 inhibitors (e.g., fluoxetine, omeprazole): may increase lacosamide exposure.
  • Anticoagulants (e.g., warfarin): monitor INR for potential changes.
  • Alcohol: may enhance central nervous system depression.
  • Other antiepileptic drugs: assess for additive sedation or efficacy changes.

Frequently Asked Questions

Lacosamidă Teva contains lacosamide, an anticonvulsant indicated for the treatment of partial‑onset (focal) seizures and as adjunctive therapy in patients with epilepsy. It helps reduce seizure frequency when added to existing antiepileptic regimens.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes. By stabilizing hyper‑excitable neurons, it limits repetitive firing and the spread of epileptic activity, thereby decreasing seizure occurrence.

The specific dose of Lacosamidă Teva is determined by the prescribing clinician based on the patient’s age, weight, renal function, and response to therapy. Dosage adjustments are individualized and should follow the prescriber’s instructions.

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 the decision should be made in consultation with a healthcare professional.

To request Lacosamidă Teva, 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 other antiepileptics that act on fast inactivation or other pathways. This can provide additive seizure control when combined with drugs like carbamazepine or levetiracetam, but clinicians must consider interaction potential and individual patient response.

Lacosamidă Teva tablets should be stored at ambient temperature, below 25 °C, in the original packaging to protect from moisture and light. Keep the container tightly closed and out of reach of children.

Lacosamidă Teva is taken orally, usually with or without food, as directed by the prescriber. The tablet should be swallowed whole with water and not chewed or crushed unless specifically instructed.

Serious risks include cardiac conduction abnormalities such as PR‑interval prolongation, severe skin reactions like Stevens‑Johnson syndrome, hepatic dysfunction, and rare cases of suicidal ideation. Patients should be monitored for these events, especially during treatment initiation and dose adjustments.

Lacosamidă Teva is contraindicated in patients with known hypersensitivity to lacosamide or any of its excipients. Caution is advised for individuals with significant cardiac conduction disorders, severe hepatic impairment, or uncontrolled renal failure, and it should be avoided in these cases unless benefits clearly outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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