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

Levetiracetam Aurovitas

Active Ingredient:
Levetiracetam
Origin:
EU

Levetiracetam Aurovitas (Levetiracetam)

Levetiracetam, the active ingredient in Levetiracetam Aurovitas, is an anticonvulsant presented as an oral formulation for oral use. It is indicated for the treatment of partial‑onset seizures, primary generalized tonic‑clonic seizures, and myoclonic seizures in patients diagnosed with epilepsy.

GNH India supplies Levetiracetam Aurovitas 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 an anticonvulsant used to control various seizure types in epilepsy.
  • Partial‑onset seizures: reduces the frequency of focal seizure episodes.
  • Primary generalized tonic‑clonic seizures: helps prevent generalized convulsive episodes.
  • 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 suppresses the propagation of seizure activity across the central nervous system.

Side Effects

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

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 cranial pain.
  • Irritability: mood changes or increased agitation.
  • Nausea: upset stomach or feeling of queasiness.

Serious or Rare Side Effects

  • Severe allergic reactions: rash, swelling, or difficulty breathing.
  • Mood alterations: depression, anxiety, or suicidal thoughts.
  • Blood disorders: leukopenia or thrombocytopenia.
  • Stevens‑Johnson syndrome: rare, severe skin reaction.
  • Hepatic dysfunction: elevated liver enzymes.
  • Respiratory depression: marked reduction in breathing effort.

Precautions & Warnings

Before initiating therapy, consider patient‑specific factors and monitor appropriately.

  • Renal impairment: adjust dose based on renal function.
  • Hepatic impairment: monitor liver function tests regularly.
  • History of psychiatric disorders: observe for mood changes or suicidal ideation.
  • Pregnancy: risk unknown; use only if potential benefit justifies the risk.
  • Concomitant alcohol use: avoid excessive intake as it may increase sedation.
  • Store at room temperature: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Levetiracetam can interact with several medications, requiring careful management.

Major Interactions (Avoid)

  • Carbamazepine: may reduce levetiracetam plasma concentrations.
  • Phenobarbital: can lower levetiracetam levels.
  • Phenytoin: may decrease levetiracetam exposure.
  • Valproic acid: may increase levetiracetam concentrations.
  • Other antiepileptics: potential additive central nervous system effects.

Moderate Interactions (Monitor Closely)

  • Oral contraceptives: efficacy may be reduced.
  • Antidepressants: monitor for mood alterations.
  • Alcohol: may potentiate sedation and dizziness.

Frequently Asked Questions

Levetiracetam Aurovitas is prescribed to control seizures in patients with epilepsy, specifically partial‑onset seizures, primary generalized tonic‑clonic seizures, and myoclonic seizures.

Levetiracetam binds to the synaptic vesicle protein SV2A, which modulates neurotransmitter release and stabilizes neuronal activity, thereby reducing the likelihood of seizure propagation.

The dosage of levetiracetam is individualized by the prescribing clinician based on the patient’s seizure type, age, renal function, and overall clinical response.

Safety data for levetiracetam in pregnancy and lactation are limited. It should only be used if the potential therapeutic benefit justifies the possible risk to the fetus or infant.

To place an order, 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.

Levetiracetam offers a favorable safety profile with fewer drug‑enzyme interactions compared with many older antiepileptics such as carbamazepine or phenytoin, making it a common choice for patients requiring monotherapy or adjunctive therapy.

Store the product at room temperature, below 25 °C, in its original packaging. Keep it away from moisture, heat, and direct sunlight to maintain stability.

Levetiracetam is taken orally, usually as tablets or oral solution, and can be taken with or without food according to the prescribing physician’s instructions.

Serious risks include severe allergic reactions, mood changes such as depression or suicidal thoughts, rare skin disorders like Stevens‑Johnson syndrome, and blood dyscrasias. Immediate medical attention is required if these occur.

Patients with known hypersensitivity to levetiracetam or any component of the formulation should avoid its use. Caution is also advised for individuals with severe renal impairment unless dose adjustments are made.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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