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

Levetiracetam Zentiva

Active Ingredient:
Levetiracetam
Origin:
EU

Levetiracetam Zentiva (Levetiracetam)

Levetiracetam, the active ingredient in Levetiracetam Zentiva, is an Anticonvulsant presented as an oral tablet for oral use. It is employed to control various types of epileptic seizures in patients requiring seizure management. The medication works by modulating neuronal activity, helping to reduce the frequency and severity of seizure episodes.

GNH India supplies Levetiracetam Zentiva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company ensures quality assurance through rigorous testing and adheres to global regulatory standards for safe distribution.

Manufacturer / TM Owner

Zentiva France

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Indications & Clinical Uses

Levetiracetam is an antiepileptic drug that targets seizure activity in the central nervous system.

  • Partial-onset seizures: Reduces frequency of focal seizures, improving seizure control.
  • Generalized tonic-clonic seizures: Decreases occurrence of bilateral convulsive episodes.
  • Myoclonic seizures: Helps prevent rapid, brief muscle jerks associated with myoclonus.

How It Works

  • Levetiracetam binds to the synaptic vesicle protein SV2A, a key regulator of neurotransmitter release. This interaction modulates synaptic vesicle exocytosis, stabilizing neuronal firing and reducing hyper‑excitability. By influencing calcium‑dependent release of glutamate and other excitatory transmitters, the drug diminishes the propagation of epileptiform activity without directly affecting ion channels or G‑protein pathways. The precise downstream effects remain under investigation, but the overall result is a net decrease in seizure susceptibility.

Side Effects

Levetiracetam may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Dizziness: Sensation of light‑headedness or unsteady balance.
  • Fatigue: Persistent tiredness or lack of energy.
  • Headache: Mild to moderate cranial pain.
  • Somnolence: Increased sleepiness during the day.
  • Irritability: Mood changes including agitation.
  • Nausea: Stomach discomfort or urge to vomit.

Serious or Rare Side Effects

  • Stevens‑Johnson syndrome: Severe skin reaction with blistering.
  • Suicidal thoughts: Emergence of depressive ideation or self‑harm urges.
  • Severe depression: Marked mood decline requiring medical attention.
  • Blood dyscrasias: Unusual drops in white blood cells or platelets.
  • Hypersensitivity reactions: Anaphylaxis or angioedema.
  • Hepatic injury: Signs of liver dysfunction such as jaundice.

Precautions & Warnings

Before prescribing Levetiracetam, clinicians should consider several precautionary measures to ensure patient safety.

  • Renal impairment: Adjust dose based on creatinine clearance.
  • Hepatic impairment: Monitor liver function tests regularly.
  • Psychiatric symptoms: Observe for mood changes, depression, or aggression.
  • Concomitant CNS depressants: Use caution as additive sedation may occur.
  • Pregnancy: Risk category unknown; discuss potential benefits and risks with the patient.
  • Store at room temperature: Keep in the original container, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Carbamazepine: Increases metabolism of levetiracetam, lowering its plasma levels.
  • Phenobarbital: Induces hepatic enzymes that reduce levetiracetam exposure.
  • Phenytoin: Accelerates clearance, potentially diminishing seizure control.

Moderate Interactions (Monitor Closely)

  • Alcohol: Combined use may enhance central nervous system depression.
  • Other antiepileptics: May require dose adjustments to maintain therapeutic effect.
  • Oral contraceptives: May experience reduced efficacy, consider alternative contraception.

Frequently Asked Questions

Levetiracetam Zentiva is prescribed to treat epilepsy. It is indicated for partial‑onset seizures, generalized tonic‑clonic seizures, and myoclonic seizures, helping to reduce the frequency and severity of seizure episodes in patients with these conditions.

Levetiracetam binds to the synaptic vesicle protein SV2A, which regulates neurotransmitter release. This binding modulates vesicle exocytosis, stabilizing neuronal firing and decreasing hyper‑excitability, thereby reducing the propagation of epileptiform activity in the brain.

The appropriate dose of Levetiracetam Zentiva is individualized by the prescribing clinician. Dosage is based on factors such as the type of seizure, patient age, renal function, and response to therapy, and should not be altered without medical guidance.

Levetiracetam is classified with an unknown pregnancy category, meaning potential risks cannot be ruled out. Women who are pregnant, planning pregnancy, or breastfeeding should discuss benefits and possible risks with their healthcare provider before using the medication.

To order Levetiracetam Zentiva, 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 distinct mechanism by targeting SV2A, which differs from many antiepileptics that modulate ion channels or G‑protein pathways. It generally has a favorable interaction profile and does not require routine therapeutic drug monitoring, making it a convenient option for many patients.

Levetiracetam Zentiva tablets should be stored at room temperature, below 25 °C, in the original packaging to protect them from moisture and light. Keep the product out of reach of children and avoid storing in humid or excessively hot environments.

Levetiracetam Zentiva is taken orally, usually with or without food, as directed by the prescriber. The tablet should be swallowed whole with water and not chewed or crushed unless specifically instructed by a healthcare professional.

Serious risks include severe skin reactions such as Stevens‑Johnson syndrome, emergence of suicidal thoughts or severe depression, and rare blood dyscrasias. Patients should seek immediate medical attention if they notice rash, mood changes, or signs of infection.

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 who may require dose adjustments, and it should be avoided in pregnancy unless clearly justified by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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