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 an anti‑epileptic 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 and is administered under medical supervision in hospital settings.

GNH India supplies Lacosamide Fresenius Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, and clinical centres worldwide, ensuring quality, regulatory compliance, and reliable delivery across global markets with dedicated customer support and traceability throughout the supply chain.

Manufacturer / TM Owner

Fresenius Kabi Ab

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Indications & Clinical Uses

Lacosamide is an anti‑epileptic that acts on neuronal sodium channels to control seizure activity. It is used in the following clinical situations:

  • Partial‑onset seizures: reduces seizure frequency as an add‑on therapy in epilepsy patients.
  • Focal epilepsy: improves overall seizure control when combined with other antiepileptic drugs.
  • Refractory epilepsy: provides an additional mechanism of action for patients not adequately controlled by existing therapies.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, stabilizing hyperexcitable neuronal membranes, and binds to collapsin response mediator protein‑2 (CRMP‑2) to modulate neuronal excitability, thereby reducing the likelihood of seizure propagation.

Side Effects

Lacosamide may cause a range of adverse reactions. Common Side Effects:

  • Dizziness: mild to moderate sensation of light‑headedness.
  • Headache: transient cranial discomfort.
  • Nausea: occasional upset stomach.
  • Fatigue: feeling of tiredness or reduced energy.
  • Blurred vision: temporary visual disturbances.
  • Somnolence: increased sleepiness.

Serious or Rare Side Effects

  • Cardiac conduction abnormalities: PR‑interval prolongation or atrial fibrillation.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hypersensitivity: rash, itching, or anaphylaxis.
  • Suicidal ideation: emergence of depressive thoughts.
  • Respiratory depression: reduced breathing effort in vulnerable patients.
  • Hepatic dysfunction: elevated liver enzymes indicating liver stress.

Precautions & Warnings

When prescribing Lacosamide, consider the following precautions:

  • Renal impairment: monitor renal function and adjust therapy as needed.
  • Cardiac conduction disorders: obtain baseline ECG and observe for PR‑interval changes.
  • Pregnancy: safety not established; weigh potential benefits against risks.
  • Concomitant CNS depressants: may increase sedation or respiratory depression.
  • Hepatic impairment: use with caution and monitor liver enzymes.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Lacosamide can interact with several medications. Major Interactions (Avoid):\n- Class I antiarrhythmics (e.g., quinidine): may exacerbate PR‑interval prolongation.

  • Carbamazepine: may reduce lacosamide plasma concentrations.
  • Other sodium‑channel blockers: risk of additive central nervous system effects.

Moderate Interactions (Monitor Closely)

  • CNS depressants (e.g., benzodiazepines, opioids): may enhance sedation.
  • Anticoagulants (e.g., warfarin): potential increased bleeding risk.
  • Hormonal contraceptives: may decrease contraceptive efficacy.

Frequently Asked Questions

Lacosamide Fresenius Kabi is an anti‑epileptic medication indicated as adjunctive therapy for partial‑onset seizures in patients with epilepsy. It is administered intravenously to help reduce the frequency of seizures when added to existing antiepileptic regimens.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, stabilizing neuronal membranes and reducing hyperexcitability. It also binds to CRMP‑2, a protein involved in neuronal development, which further modulates neuronal excitability and helps prevent seizure propagation.

The specific dose and infusion rate of lacosamide are determined by the prescribing clinician based on the patient’s clinical condition, weight, renal function, and response to therapy. Dosing should follow the approved prescribing information and be individualized for each patient.

Safety data for lacosamide in pregnancy and lactation are limited, and the pregnancy category is listed as unknown. Clinicians should carefully weigh the potential benefits against possible risks and consider alternative therapies when treating pregnant or nursing patients.

To order Lacosamide Fresenius Kabi, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies, and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details, and any necessary import documentation.

Lacosamide has a unique mechanism that enhances slow inactivation of sodium channels, differing from many traditional sodium‑channel blockers that affect fast inactivation. This can provide an additional therapeutic option for patients who have inadequate seizure control with other antiepileptics, though individual response varies.

Lacosamide intravenous solution should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use and follow any additional handling instructions provided by the manufacturer.

Lacosamide Fresenius Kabi is given as an intravenous infusion under medical supervision. The infusion rate and duration are set by the healthcare professional according to the patient’s clinical needs and the product’s prescribing information.

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

Lacosamide is contraindicated in patients with known hypersensitivity to the drug or any of its excipients. Caution is advised for individuals with significant cardiac conduction disorders, severe hepatic impairment, or those taking other medications that may cause additive CNS depression.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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