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 is indicated for the treatment of partial seizures, generalized tonic‑clonic seizures and myoclonic seizures in patients diagnosed with epilepsy, and is marketed throughout the European Union.

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

Manufacturer / TM Owner

Eg S.P.A.

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Indications & Clinical Uses

Levetiracetam is an antiepileptic drug used to control various seizure types.

  • Partial seizures: reduces the frequency and severity of focal onset seizures.
  • Generalized tonic‑clonic seizures: helps prevent convulsive episodes that involve the whole brain.
  • Myoclonic seizures: diminishes sudden, brief muscle jerks associated with myoclonic epilepsy.

How It Works

  • Levetiracetam binds to the synaptic vesicle protein SV2A, a key regulator of neurotransmitter release. This interaction modulates synaptic transmission, decreasing neuronal excitability and stabilising abnormal electrical activity that underlies seizure generation.

Side Effects

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

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Fatigue: feeling unusually tired or low in energy.
  • Headache: mild to moderate pain in the head region.
  • Irritability: increased emotional sensitivity or agitation.
  • Nausea: mild upset stomach or urge to vomit.
  • Nasal congestion: blocked or runny nose.

Serious or Rare Side Effects

  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Mood changes: including depression, suicidal thoughts, or aggression.
  • Hematologic abnormalities: rare cases of low blood cell counts.
  • Hepatic dysfunction: elevated liver enzymes indicating liver stress.
  • Respiratory depression: uncommon but potentially life‑threatening breathing difficulty.
  • Anaphylaxis: rare severe allergic response requiring immediate medical attention.

Precautions & Warnings

Before initiating therapy, consider the following precautions.

  • Pregnancy: Category B – use only if potential benefit justifies the potential risk to the fetus.
  • Renal impairment: dose may need adjustment in patients with reduced kidney function.
  • Psychiatric history: monitor for mood changes, especially in patients with prior depression or anxiety.
  • Concomitant CNS depressants: may enhance sedation or dizziness.
  • Driving and machinery: avoid operating heavy equipment until individual response is known.
  • Store at ambient temperature: keep below 25°C, retain in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Carbamazepine: may reduce levetiracetam plasma levels, decreasing seizure control.
  • Phenobarbital: can lower levetiracetam concentrations, potentially compromising effectiveness.

Moderate Interactions (Monitor Closely)

  • Valproic acid: may increase levetiracetam levels, requiring clinical monitoring.
  • Rifampin: can induce metabolism, lowering levetiracetam exposure.
  • Oral contraceptives: levetiracetam may reduce hormonal contraceptive efficacy; advise alternative birth control.
  • Alcohol: may exacerbate central nervous system depression and dizziness.
  • Other antiepileptics: combined use may increase risk of adverse CNS effects.

Frequently Asked Questions

Levetiracetam Eg is an antiepileptic medication indicated for the treatment of 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 abnormal neuronal activity.

Levetiracetam exerts its effect by binding to the synaptic vesicle protein SV2A, which plays a crucial role in regulating neurotransmitter release. This binding modulates synaptic transmission, leading to decreased neuronal excitability and reduced likelihood of seizure generation.

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

Levetiracetam is classified as Pregnancy Category B, indicating that animal studies have not shown risk, but there are limited human data. It may be used during pregnancy only if the potential benefit justifies any potential risk. Limited data suggest it is excreted in breast milk; breastfeeding decisions should be made in consultation with a healthcare professional.

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, and will request verification of trade or institutional credentials. The sales team will then respond with pricing, availability, shipping details (including any cold‑chain requirements) and necessary import documentation.

Compared with many traditional antiepileptics, levetiracetam has a relatively simple pharmacokinetic profile, minimal protein binding, and fewer drug‑enzyme interactions. This can make dosing more predictable and reduce the need for routine therapeutic drug monitoring, although individual response and side‑effect profiles still guide drug selection.

Levetiracetam Eg should be stored at ambient temperature, below 25 °C. Keep the tablets in their original container, protect them from moisture, excessive heat and direct sunlight to maintain product stability.

Levetiracetam Eg is supplied as oral tablets and is taken by mouth with or without food, as directed by the prescriber. Swallow the tablet whole; do not crush, chew, or split unless specifically advised by a healthcare professional.

Serious risks include severe skin reactions such as Stevens‑Johnson syndrome, mood alterations including depression or suicidal thoughts, and rare hematologic abnormalities. Patients should be monitored for any signs of rash, mood changes, or unusual bleeding, and seek immediate medical attention if these occur.

Levetiracetam 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 adjustment may be required, and for those with a history of serious psychiatric disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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