Product image of Midza (Lacosamide) supplied by GNH India

Midza

Active Ingredient:
Lacosamide
Origin:
EU

Midza (Lacosamide)

Lacosamide, the active ingredient in Midza, 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. It is formulated for systemic absorption and is marketed across the European Union. The product meets stringent regulatory requirements for safety and efficacy.

GNH India supplies Midza as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, adhering to EU quality standards and providing reliable global distribution.

Manufacturer / TM Owner

Belupo D.D.

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Indications & Clinical Uses

Lacosamide is an anticonvulsant that acts on neuronal sodium channels to control seizure activity.

  • Partial‑onset seizures: reduces the frequency and severity of focal seizures.
  • Adjunctive therapy for epilepsy: enhances seizure control when added to existing antiepileptic regimens.
  • Epilepsy (generalized): may be employed as part of a broader treatment plan under specialist guidance.

How It Works

  • Lacosamide enhances the slow inactivation of voltage‑gated sodium channels, stabilizing hyperexcitable neuronal membranes. By selectively targeting the persistent sodium current, it diminishes repetitive neuronal firing, thereby reducing the propagation of seizure activity without significantly affecting normal neuronal function.

Side Effects

Lacosamide may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Nausea: mild to moderate stomach upset.
  • Headache: transient cranial discomfort.
  • Fatigue: unusual tiredness or lack of energy.
  • Blurred vision: temporary visual disturbances.
  • Diplopia: double vision in some patients.

Serious or Rare Side Effects

  • Suicidal ideation: emergence of thoughts of self‑harm.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Cardiac arrhythmias: including PR‑interval prolongation.
  • Respiratory depression: marked reduction in breathing effort, especially when combined with other CNS depressants.

Precautions & Warnings

When prescribing or dispensing Lacosamide, clinicians should consider several safety measures.

  • Cardiac monitoring: assess ECG for PR‑interval changes before initiation.
  • Renal function: adjust dosing in patients with impaired clearance.
  • Concomitant CNS depressants: evaluate additive sedation risk.
  • Patient counseling: advise on dizziness and advise against operating machinery until tolerance is known.
  • Discontinuation: avoid abrupt cessation to prevent seizure rebound.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase lacosamide plasma levels.
  • Strong CYP3A4 inducers (e.g., carbamazepine, phenytoin): may reduce lacosamide exposure.
  • Other sodium‑channel blockers (e.g., lamotrigine): increase risk of CNS depression.
  • Alcohol: potentiates dizziness and sedation.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: additive hypotensive effect may require dose adjustment.
  • Oral contraceptives: lacosamide may reduce hormonal efficacy, consider alternative contraception.
  • Other antiepileptics (e.g., valproate): may necessitate therapeutic drug monitoring.

Frequently Asked Questions

Midza contains the active ingredient lacosamide and is prescribed to treat partial‑onset seizures. It is also used as adjunctive therapy in patients with epilepsy to improve overall seizure control when added to other antiepileptic drugs.

Lacosamide enhances the slow inactivation of voltage‑gated sodium channels in neuronal membranes. This stabilizes hyper‑excitable neurons, reduces repetitive firing, and thereby diminishes the spread of seizure activity without markedly affecting normal brain function.

The dosage of Midza is individualized by the prescribing clinician based on the patient’s age, weight, renal function, and response to therapy. The prescriber determines the appropriate starting dose and any subsequent titration schedule.

The pregnancy category for lacosamide is listed as unknown, indicating limited data on fetal risk. Women who are pregnant, planning pregnancy, or breastfeeding should discuss potential benefits and risks with their healthcare provider before using Midza.

To request Midza, 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.

Midza (lacosamide) offers a unique mechanism by enhancing slow sodium‑channel inactivation, which differs from many traditional antiepileptics that block fast sodium channels or modulate GABA. This can provide additional seizure control for patients who have not responded adequately to other classes.

Midza should be stored at room temperature, below 25 °C. Keep the tablets in the original packaging, protect them from moisture and direct sunlight, and ensure the container is tightly closed to maintain product stability.

Midza is taken orally, usually with or without food, as directed by the prescriber. The tablets should be swallowed whole with a glass of water and not crushed or chewed unless specifically instructed.

Serious risks include the potential for suicidal thoughts or behavior, severe skin reactions such as Stevens‑Johnson syndrome, and cardiac conduction abnormalities like PR‑interval prolongation. Patients should be monitored closely for any of these events.

Midza is contraindicated in patients with known hypersensitivity to lacosamide or any of its excipients. Caution is also advised for individuals with significant cardiac conduction disorders, severe renal impairment, or those taking interacting medications that could increase toxicity.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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