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

Levetiracetam Generis

Active Ingredient:
Levetiracetam
Origin:
EU

Levetiracetam Generis (Levetiracetam)

Levetiracetam, the active ingredient in Levetiracetam Generis, is an antiepileptic presented as an oral tablet for oral use. It is indicated for the treatment of partial, generalized tonic‑clonic and myoclonic seizures in patients with epilepsy.

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

Manufacturer / TM Owner

Generis Farmacêutica, S.A.

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Indications & Clinical Uses

  • Levetiracetam is used to control various seizure types within the epileptic disorder spectrum.
  • Partial seizures: reduces the frequency of focal onset seizures in patients with epilepsy.
  • Generalized tonic‑clonic seizures: helps prevent convulsive episodes in generalized epilepsy.
  • Myoclonic seizures: decreases myoclonic jerks in appropriate patient populations.

How It Works

  • Levetiracetam binds selectively to the synaptic vesicle protein SV2A, a key regulator of neurotransmitter release. This interaction modulates synaptic transmission, stabilizing neuronal firing and reducing hyperexcitability in the central nervous system, which underlies its anticonvulsant effect.

Side Effects

Levetiracetam may cause a range of adverse reactions, which are categorized by frequency.

Common Side Effects

  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Somnolence: increased sleepiness or fatigue.
  • Headache: mild to moderate cranial pain.
  • Irritability: mood changes or agitation.
  • Nausea: mild gastrointestinal discomfort.
  • Fatigue: general lack of energy.

Serious or Rare Side Effects

  • Severe allergic reactions: rash, swelling, or anaphylaxis.
  • Psychiatric events: depression, suicidal thoughts, or aggressive behavior.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis: rare severe skin reactions.
  • Blood dyscrasias: neutropenia or thrombocytopenia.
  • Hepatic dysfunction: elevated liver enzymes or hepatitis.

Precautions & Warnings

  • Before initiating therapy, clinicians should consider several safety aspects.
  • Renal impairment: adjust dose based on creatinine clearance.
  • Psychiatric monitoring: observe for mood changes, depression, or suicidal ideation.
  • Abrupt discontinuation: taper gradually to avoid seizure exacerbation.
  • Elderly patients: start at lower dose and monitor tolerability.
  • Hypersensitivity: avoid in patients with known allergy to levetiracetam.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Carbamazepine: induces metabolism, reducing levetiracetam plasma levels.
  • Phenytoin: enzyme induction may lower levetiracetam concentrations.
  • Rifampin: strong inducer that can decrease levetiracetam exposure.

Moderate Interactions (Monitor Closely)

  • Cimetidine: may increase levetiracetam levels modestly.
  • Oral contraceptives: levetiracetam may reduce hormonal efficacy; consider alternative contraception.
  • Alcohol: additive CNS depression may enhance somnolence.

Frequently Asked Questions

Levetiracetam Generis 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 these seizure types when used as part of a comprehensive treatment plan.

Levetiracetam exerts its anticonvulsant effect by binding to the synaptic vesicle protein SV2A. This binding modulates neurotransmitter release, stabilizing neuronal firing and decreasing hyperexcitability in the brain, which in turn helps prevent the initiation and spread of seizure activity.

The appropriate dose of Levetiracetam Generis is determined by the prescribing clinician based on the patient’s age, renal function, seizure type, and response to therapy. Dosage adjustments may be required for special populations, and the prescriber will provide individualized instructions.

Safety data for levetiracetam in pregnancy and lactation are limited, and the pregnancy category is listed as unknown. Clinicians should weigh the potential benefits against possible risks and discuss options with the patient. Breastfeeding decisions should also 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. After verification of trade or institutional credentials, the sales team will respond with 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 minimal drug‑enzyme interactions, and does not require routine therapeutic monitoring, making it a convenient option for many patients.

Levetiracetam Generis should be stored at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed to maintain stability.

Levetiracetam Generis is taken orally, usually with or without food, as directed by the prescriber. The tablets should be swallowed whole with a glass of water. If a patient has difficulty swallowing, the prescriber may consider an alternative formulation.

Serious risks include severe allergic reactions such as Stevens‑Johnson syndrome, psychiatric events like depression or suicidal thoughts, and rare blood disorders. Patients should be instructed to seek immediate medical attention if they experience rash, mood changes, or signs of infection.

Levetiracetam Generis is contraindicated in individuals with a known hypersensitivity to levetiracetam or any of its excipients. Caution is also advised for patients with severe renal impairment who have not had dose adjustments, 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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