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

Levetiracetam Eg

Active Ingredient:
Levetiracetam
Origin:
EU

Levetiracetam Eg (Levetiracetam)

Levetiracetam, the active ingredient in Levetiracetam Eg, is an anticonvulsant presented as an oral tablet for oral use. It treats partial seizures, generalized tonic‑clonic seizures and myoclonic seizures in patients with epilepsy.

GNH India supplies Levetiracetam Eg 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 used to control various seizure types.
  • Partial seizures: reduces the frequency of focal seizure episodes.
  • Generalized tonic‑clonic seizures: helps prevent convulsive seizures across both brain hemispheres.
  • Myoclonic seizures: diminishes rapid, involuntary muscle jerks associated with myoclonic epilepsy.

How It Works

  • Levetiracetam binds to the synaptic vesicle protein SV2A, modulating neurotransmitter release and stabilizing neuronal membranes. This action reduces neuronal hyperexcitability and limits the propagation of seizure activity throughout the central nervous system.

Side Effects

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

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Fatigue: feeling unusually tired or weak.
  • Somnolence: increased sleepiness during the day.
  • Headache: mild to moderate head pain.
  • Irritability: mood changes or increased agitation.
  • Nausea: upset stomach or feeling of queasiness.

Serious or Rare Side Effects

  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Suicidal thoughts: emergence of depressive or suicidal ideation.
  • Severe depression: marked mood disturbances requiring medical attention.
  • Blood disorders: rare cases of leukopenia or thrombocytopenia.
  • Allergic reactions: anaphylaxis or angioedema.
  • Multi‑organ involvement: rare systemic hypersensitivity.

Precautions & Warnings

  • Before initiating levetiracetam therapy, consider the following safety measures.
  • Renal impairment: dose may need adjustment based on kidney function.
  • Pregnancy: potential risk unknown; discuss benefits and risks with a healthcare professional.
  • Concomitant CNS depressants: monitor for enhanced sedation or respiratory depression.
  • Psychiatric symptoms: observe for mood changes, aggression, or suicidal thoughts.
  • Store below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Carbamazepine: may lower levetiracetam plasma concentrations.
  • Phenytoin: can reduce levetiracetam levels, decreasing seizure control.
  • Phenobarbital: may decrease levetiracetam exposure.

Moderate Interactions (Monitor Closely)

  • Alcohol: combined use may increase central nervous system depression.
  • Other antiepileptics: may require dose adjustments to maintain therapeutic effect.
  • Oral contraceptives: levetiracetam may reduce hormonal contraceptive efficacy.

Frequently Asked Questions

Levetiracetam Eg is prescribed for the management of partial (focal) seizures, generalized tonic‑clonic seizures, and myoclonic seizures in patients diagnosed with epilepsy. It helps reduce the frequency and severity of seizure episodes across these seizure types.

Levetiracetam binds to the synaptic vesicle protein SV2A in the brain, modulating neurotransmitter release. This stabilizes neuronal firing and decreases hyper‑excitability, thereby limiting the spread of seizure activity throughout the central nervous system.

The specific dose of Levetiracetam Eg is determined by the prescribing clinician based on the patient’s age, weight, renal function, and seizure type. Dosage adjustments are individualized and should follow the prescriber’s instructions.

Safety data for levetiracetam in pregnancy are limited, and the pregnancy category is listed as unknown. Women who are pregnant, planning pregnancy, or breastfeeding should discuss potential risks and benefits with their healthcare provider before using the medication.

To request Levetiracetam Eg, 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 distinct mechanism by targeting SV2A, which differs from sodium‑channel blockers like carbamazepine or GABA‑enhancers such as valproate. It is generally well‑tolerated, has fewer drug‑enzyme interactions, and can be used as monotherapy or adjunct therapy, making it a versatile option in epilepsy management.

Levetiracetam Eg should be stored at temperatures below 25 °C. Keep the tablets in their original container, protect them from moisture and direct sunlight, and ensure the packaging remains sealed until use.

Levetiracetam Eg is taken orally, usually as a tablet. It can be swallowed whole with water and may be taken with or without food, according to the prescriber’s guidance.

Serious risks include severe skin reactions such as Stevens‑Johnson syndrome, emergence of suicidal thoughts or severe depression, and rare blood disorders. Patients should promptly report any rash, mood changes, or unusual bleeding to their healthcare provider.

Levetiracetam Eg is contraindicated in individuals with known hypersensitivity to levetiracetam or any of its excipients. Caution is also advised for patients with severe renal impairment, as dose adjustments may be required.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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