Product image of Lacosamide Hikma Farmacêutica (Lacosamide) supplied by GNH India

Lacosamide Hikma Farmacêutica

Active Ingredient:
Lacosamide
Origin:
EU

Lacosamide Hikma Farmacêutica (Lacosamide)

Lacosamide, the active ingredient in Lacosamide Hikma Farmacêutica, is an anti-epileptic drug presented as an intravenous solution for intravenous use. It is used as adjunctive therapy for partial‑onset seizures and primary generalized tonic‑clonic seizures in patients who require additional seizure control.

GNH India supplies Lacosamide Hikma Farmacêutica as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, clinics and pharmacy networks worldwide. The company adheres to stringent quality standards and provides regulatory documentation for global distribution.

Manufacturer / TM Owner

Hikma Farmacêutica (Portugal), S.A.

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Indications & Clinical Uses

Lacosamide is an anticonvulsant indicated for the treatment of epilepsy, specifically targeting seizure types that arise from abnormal neuronal firing.

  • Partial‑onset seizures: used as adjunctive therapy to reduce seizure frequency in patients with focal epilepsy.
  • Primary generalized tonic‑clonic seizures: added to existing regimens to improve control of generalized seizures.
  • Status epilepticus (intravenous use): may be employed in acute settings when rapid seizure control is required.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, stabilizing hyper‑excitable neuronal membranes and reducing repetitive neuronal firing. By selectively modulating this channel state, it diminishes the propagation of epileptiform activity without markedly affecting normal conduction, providing complementary seizure control to other sodium‑channel blockers.

Side Effects

Lacosamide may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Dizziness: sensation of light‑headedness or imbalance.
  • Nausea: mild to moderate gastrointestinal discomfort.
  • Headache: transient cranial pain.
  • Fatigue: generalized tiredness.
  • Vision changes: blurred or double vision.
  • Tremor: involuntary shaking of limbs.

Serious or Rare Side Effects

  • Cardiac arrhythmias: including PR‑interval prolongation.
  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Respiratory depression: reduced breathing effort.
  • Hypotension: significant drop in blood pressure.

Precautions & Warnings

When prescribing Lacosamide, clinicians should consider several safety and handling precautions.

  • Renal impairment: adjust monitoring as the drug is renally excreted.
  • Cardiac conduction disorders: evaluate ECG for PR‑interval changes.
  • Concomitant CNS depressants: monitor for enhanced sedation.
  • Pregnancy: use only if potential benefit justifies potential risk, as data are limited.
  • Elderly patients: start at lower doses and observe for tolerance.
  • Store at ambient temperature: keep below 25 °C, protect from moisture and light in the original container.

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., carbamazepine, oxcarbazepine): increased risk of cardiac conduction effects.

Moderate Interactions (Monitor Closely)

  • Anticoagulants (e.g., warfarin): may require INR monitoring.
  • Opioids or benzodiazepines: additive CNS depression.
  • Alcohol: enhances sedative effects.
  • Contraceptive hormones: possible reduction in efficacy.

Frequently Asked Questions

Lacosamide is used as an adjunctive therapy in epilepsy to treat partial‑onset seizures and primary generalized tonic‑clonic seizures. It may also be administered intravenously in acute settings such as status epilepticus when rapid seizure control is needed.

Lacosamide enhances the slow inactivation phase of voltage‑gated sodium channels in neuronal membranes. This stabilizes hyper‑excitable neurons, reduces repetitive firing, and limits the spread of epileptiform activity without significantly affecting normal neuronal conduction.

The dosage of Lacosamide is individualized by the prescribing clinician based on the patient’s clinical condition, age, renal function, and response to therapy. The prescriber determines the appropriate dose and titration schedule.

Safety data for Lacosamide in pregnancy are limited, and the drug is classified as having an unknown pregnancy category. It should only be used if the potential benefit justifies any potential risk to the fetus. Breastfeeding considerations should be discussed with a healthcare professional.

To 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 if required) and necessary import documentation.

Lacosamide’s unique mechanism—enhancing slow sodium‑channel inactivation—differs from many traditional sodium‑channel blockers that affect fast inactivation. This can provide complementary seizure control and may be better tolerated in some patients, though individual response varies and choice of therapy should be guided by clinical assessment.

Lacosamide intravenous solution should be stored at ambient temperature, below 25 °C, in its original packaging. Protect it from moisture and direct light. Do not freeze the solution, and ensure the container is kept sealed until use.

Lacosamide is supplied as an intravenous solution and is administered by slow infusion into a vein under medical supervision. The rate and duration of infusion are determined by the treating physician according to the clinical situation.

Serious risks include cardiac arrhythmias such as PR‑interval prolongation, severe skin reactions like Stevens‑Johnson syndrome, respiratory depression, and significant hypotension. Patients should be monitored for these events, especially when combined with other cardiac or CNS‑depressant agents.

Lacosamide should be avoided in patients with known hypersensitivity to the drug, those with severe cardiac conduction disorders (e.g., uncontrolled PR‑interval prolongation), and individuals for whom the risk outweighs the benefit as determined by a qualified healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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