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

Lacosamid Teva

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamid Teva (Lacosamide)

Lacosamide, the active ingredient in Lacosamid Teva, is an anti‑epileptic drug presented as an oral formulation for oral use. It is indicated as adjunctive therapy for partial‑onset seizures in patients with epilepsy, helping to reduce seizure frequency when added to existing treatment regimens.

GNH India supplies Lacosamid 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

Lacosamide is used in the management of seizure disorders, specifically targeting focal epileptic activity.

  • Partial‑onset seizures: reduces seizure frequency when used as adjunctive therapy.
  • Focal seizures: improves control of seizure episodes in refractory cases.
  • Adjunctive therapy in refractory epilepsy: provides additional seizure reduction when other agents are insufficient.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, which stabilizes hyperexcitable neuronal membranes and diminishes repetitive neuronal firing. By selectively targeting the sodium channel's slow inactivation pathway, it reduces the likelihood of seizure propagation without significantly affecting normal neuronal activity.

Side Effects

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

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Fatigue: feeling unusually tired or low in energy.
  • Nausea: mild to moderate stomach upset.
  • Headache: occasional mild to moderate pain.
  • Diplopia: temporary double vision.
  • Somnolence: increased sleepiness.

Serious or Rare Side Effects

  • Suicidal ideation: thoughts of self‑harm requiring immediate evaluation.
  • Cardiac conduction abnormalities: PR‑interval prolongation that may lead to arrhythmia.
  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.
  • Anaphylaxis: severe allergic response.
  • Blood dyscrasias: rare cases of agranulocytosis or thrombocytopenia.

Precautions & Warnings

When prescribing Lacosamide, clinicians should consider several safety aspects.

  • Renal impairment: dose may need adjustment and renal function monitoring.
  • Hepatic impairment: monitor liver enzymes and consider dose modification.
  • Cardiac conduction: obtain baseline ECG and monitor for PR‑interval changes.
  • Pregnancy: risk unknown; use only if potential benefit justifies the risk.
  • Concomitant CNS depressants: may increase sedation; observe patient response.
  • Store at ambient temperature: keep in original packaging, protect from moisture and excessive heat.

Avoid Interactions

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

Major Interactions (Avoid)

  • Carbamazepine: induces metabolism, reducing lacosamide plasma levels.
  • Phenytoin: strong enzyme inducer that lowers lacosamide concentrations.
  • Strong CYP3A4 inducers (e.g., rifampin): may decrease therapeutic effect.

Moderate Interactions (Monitor Closely)

  • CNS depressants (e.g., benzodiazepines): may enhance sedation and dizziness.
  • Alcohol: can increase central nervous system effects.
  • Other anti‑epileptic drugs: monitor seizure control and adjust doses as needed.

Frequently Asked Questions

Lacosamid Teva contains lacosamide, an anti‑epileptic medication indicated as adjunctive therapy for partial‑onset (focal) seizures in patients with epilepsy. It is added to existing antiseizure regimens to help reduce the frequency of seizure episodes.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes. This stabilizes hyperexcitable neurons, limits repetitive firing, and thereby reduces the propagation of seizure activity without markedly affecting normal neuronal signaling.

The specific dose of Lacosamid Teva is determined by the prescribing clinician based on the individual patient's clinical condition, age, renal and hepatic function, and response to therapy. The prescriber will set the appropriate dosing schedule.

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 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 agents that target fast inactivation. This can offer complementary seizure control when combined with other antiseizure medicines, and it may have a distinct side‑effect profile compared with drugs such as carbamazepine or levetiracetam.

Lacosamid Teva should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight, and excessive heat to maintain its stability and potency.

Lacosamid Teva is administered orally. The tablet (or other oral form) is taken by mouth with or without food, as directed by the prescribing physician. Swallow the medication whole; do not crush or chew unless specifically instructed.

Serious risks include potential cardiac conduction abnormalities such as PR‑interval prolongation, suicidal thoughts or behavior, severe skin reactions like Stevens‑Johnson syndrome, and rare cases of hepatic dysfunction or blood disorders. Patients should be monitored regularly for these events.

Lacosamid Teva is contraindicated in individuals with known hypersensitivity to lacosamide or any of its excipients. Caution is also advised for patients with significant cardiac conduction disorders, severe hepatic impairment, or those taking strong enzyme inducers that may markedly reduce its effectiveness.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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