Product image of Lacosamide Fresenius Kabi (Lacosamide) supplied by GNH India

Lacosamide Fresenius Kabi

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamide Fresenius Kabi (Lacosamide)

Lacosamide, the active ingredient in Lacosamide Fresenius Kabi, is a sodium channel blocker presented as an intravenous solution for intravenous use. It is indicated as adjunctive therapy for partial‑onset seizures in patients with epilepsy, helping to reduce seizure frequency.

GNH India supplies Lacosamide Fresenius Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, clinics and research institutions worldwide, providing EU‑origin products that meet stringent quality standards.

Manufacturer / TM Owner

Fresenius Kabi France S.A.S.

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Indications & Clinical Uses

Lacosamide is an antiepileptic drug used in the management of seizure disorders.

  • Partial‑onset seizures: reduces seizure frequency when added to existing antiepileptic regimens.
  • Focal epilepsy: improves seizure control in patients with focal onset epilepsy.
  • Epilepsy (adjunctive therapy): provides additional seizure reduction for patients whose seizures are not fully controlled by other medications.

How It Works

  • Lacosamide selectively enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes, stabilizing hyper‑excitable neuronal membranes and decreasing repetitive neuronal firing that contributes to seizure activity. By shifting the equilibrium toward the non‑conducting state of the channel, it reduces the ability of neurons to fire at high frequencies, thereby attenuating the propagation of epileptic discharges without significantly affecting normal neuronal function. This mechanism is distinct from fast‑inactivation blockers and provides a complementary approach when combined with other antiepileptic agents.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Dizziness: sensation of lightheadedness.
  • Headache: mild to moderate head pain.
  • Fatigue: feeling of tiredness or reduced energy.

Serious or Rare Side Effects

  • Cardiac conduction abnormalities: PR interval prolongation or atrial fibrillation.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Suicidal thoughts: emergence of depressive symptoms or suicidal ideation.

Precautions & Warnings

When using Lacosamide, several precautions should be observed to ensure patient safety.

  • Monitor cardiac function: obtain baseline ECG and watch for PR interval prolongation.
  • Assess renal function: adjust dosing in patients with severe renal impairment.
  • Avoid abrupt discontinuation: taper to prevent increased seizure frequency.
  • Use caution in hepatic impairment: monitor liver enzymes regularly.
  • Pregnancy and lactation: safety not established; weigh benefits against potential risks.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

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

Major Interactions (Avoid)

  • Co‑administration with other sodium channel blockers (e.g., carbamazepine) may increase cardiac conduction effects.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole) can raise lacosamide plasma concentrations.
  • Drugs that prolong PR interval (e.g., verapamil) may cause additive cardiac effects.

Moderate Interactions (Monitor Closely)

  • Combination with other antiepileptics (e.g., valproate) may require dose adjustments.
  • Concurrent use with alcohol may enhance central nervous system depression.
  • Diuretics may alter electrolyte balance, influencing cardiac conduction.

Frequently Asked Questions

Lacosamide Fresenius Kabi is an intravenous antiepileptic medication indicated as adjunctive therapy for partial‑onset seizures in patients with epilepsy. It is used when additional seizure control is needed beyond existing oral antiepileptic regimens.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes. This stabilizes hyper‑excitable neurons, reduces repetitive firing, and limits the spread of epileptic discharges, thereby decreasing seizure frequency.

The appropriate dose of lacosamide is determined by the prescribing healthcare professional based on the individual patient's clinical condition, age, renal function, and response to therapy. Specific dosing regimens are not provided here.

Safety data for lacosamide in pregnancy and lactation are limited. It is classified as pregnancy category unknown, and the decision to use it should involve a careful risk‑benefit assessment by the prescriber, considering potential effects on the fetus or infant.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where required) and necessary import documentation.

Compared with other sodium‑channel antiepileptics such as carbamazepine, lacosamide uniquely enhances slow inactivation rather than fast inactivation, offering a different mechanism that can be complementary. It is often chosen for patients who need additional seizure control without the enzyme‑inducing properties of some alternatives.

Lacosamide Fresenius Kabi should be stored at 2‑8 °C in a refrigerator, protected from light. The solution must not be frozen or shaken. Keep the product in its original packaging to maintain stability until it is prepared for intravenous administration.

Lacosamide is supplied as an intravenous solution that is administered by slow infusion into a vein under medical supervision. The infusion rate and duration are set by the healthcare professional according to the prescribed dosing schedule.

Serious risks include cardiac conduction abnormalities such as PR‑interval prolongation or atrial fibrillation, severe skin reactions like Stevens‑Johnson syndrome, and emergence of suicidal thoughts or depressive symptoms. Patients should be monitored closely for these events, especially during treatment initiation or dose changes.

Lacosamide should be avoided in individuals with known hypersensitivity to the drug or its excipients, and in patients with significant cardiac conduction disorders (e.g., existing PR‑interval prolongation) unless closely monitored. Caution is also advised for those with severe renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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