Product image of Levetiracetam Eg Labo (Levetiracetam) supplied by GNH India

Levetiracetam Eg Labo

Active Ingredient:
Levetiracetam
Origin:
EU

Levetiracetam Eg Labo (Levetiracetam)

Levetiracetam, the active ingredient in Levetiracetam Eg Labo, is an anticonvulsant presented as an oral formulation for oral use. It is indicated for the treatment of various seizure types in patients diagnosed with epilepsy.

GNH India supplies Levetiracetam Eg Labo as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Eg Labo Laboratoires Eurogenerics

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Indications & Clinical Uses

  • Levetiracetam is an antiepileptic drug that modulates neuronal excitability and is used across several seizure disorders.
  • Partial seizures: reduces the frequency and severity of focal onset seizures.
  • Generalized tonic‑clonic seizures: helps control convulsive episodes that involve the whole brain.
  • Myoclonic seizures: diminishes rapid, involuntary muscle jerks associated with myoclonic epilepsy.

How It Works

  • Levetiracetam binds selectively to the synaptic vesicle protein SV2A, a key regulator of neurotransmitter release. This interaction modulates synaptic transmission, decreasing excessive neuronal firing and stabilising neuronal networks, which results in reduced seizure activity across multiple epilepsy syndromes.

Side Effects

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

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Fatigue: persistent tiredness or lack of energy.
  • Somnolence: increased sleepiness during the day.
  • Headache: mild to moderate cranial pain.
  • Nausea: upset stomach or feeling of queasiness.

Serious or Rare Side Effects

  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Psychiatric changes: depression, anxiety, or suicidal thoughts.
  • Blood disorders: leukopenia, thrombocytopenia, or anemia.
  • Severe allergic reactions: anaphylaxis or angioedema.
  • Multi‑organ hypersensitivity: systemic inflammatory response affecting liver, kidney or lungs.

Precautions & Warnings

  • Before initiating therapy, clinicians should assess individual risk factors and monitor patients regularly.
  • Monitor renal function: adjust dose in patients with impaired kidney function.
  • Assess psychiatric status: watch for mood changes, depression or suicidal ideation.
  • Avoid abrupt discontinuation: taper gradually to prevent seizure worsening.
  • Use caution in pregnancy: limited data, weigh benefits against potential risks.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Levetiracetam can interact with other medicines, influencing its effectiveness or safety.

Major Interactions (Avoid)

  • Carbamazepine: induces metabolism, reducing levetiracetam levels.
  • Phenytoin: increases clearance, potentially decreasing efficacy.
  • Phenobarbital: may lower plasma concentrations of levetiracetam.

Moderate Interactions (Monitor Closely)

  • Valproic acid: may increase levetiracetam exposure.
  • Oral contraceptives: possible reduction in hormonal efficacy.
  • Antidepressants: monitor for additive central nervous system effects.
  • Antipsychotics: watch for enhanced sedation.
  • NSAIDs: observe for increased risk of renal impairment.

Frequently Asked Questions

Levetiracetam Eg Labo is an oral antiepileptic medication used to treat partial seizures, generalized tonic‑clonic seizures and myoclonic seizures in patients with epilepsy. It helps reduce the frequency and severity of seizure episodes by stabilising neuronal activity.

Levetiracetam binds to the synaptic vesicle protein SV2A, which plays a crucial role in neurotransmitter release. This binding modulates synaptic transmission, decreasing excessive neuronal firing and thereby lowering the likelihood of seizure generation across various epilepsy types.

The appropriate dose of levetiracetam is determined by the prescribing clinician based on the patient’s age, weight, renal function and seizure type. Dosage regimens are individualized and should follow the prescriber’s instructions and local prescribing guidelines.

Safety data for levetiracetam in pregnancy and lactation are limited. Clinicians should weigh the potential benefits for seizure control against any possible risks to the fetus or infant. Consultation with a specialist is recommended before use in pregnant or nursing women.

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 and any necessary import documentation.

Levetiracetam offers a favorable safety profile and minimal drug‑enzyme interactions compared with many older antiepileptics such as carbamazepine or phenytoin. It is often chosen for its broad spectrum of activity across seizure types and its ease of dosing, though individual response varies.

Store the product at room temperature, preferably below 25 °C. Keep it in the original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed to maintain product stability.

Levetiracetam Eg Labo is taken orally, usually with or without food, as directed by the prescriber. The tablets are swallowed whole with a glass of water and the dosing schedule (once or twice daily) is individualized for each patient.

Serious risks include severe skin reactions such as Stevens‑Johnson syndrome, psychiatric changes like depression or suicidal thoughts, and rare blood disorders (e.g., leukopenia). Patients should be monitored closely for any new or worsening symptoms and seek medical attention promptly.

Levetiracetam is contraindicated in individuals with known hypersensitivity to the drug or any of its excipients. Caution is advised for patients with severe renal impairment, uncontrolled psychiatric conditions, or those who are pregnant without a clear benefit‑risk assessment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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