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

Levetiracetam Zydus

Active Ingredient:
Levetiracetam
Origin:
EU

Levetiracetam Zydus (Levetiracetam)

Levetiracetam, the active ingredient in Levetiracetam Zydus, is an anticonvulsant presented as an oral tablet for oral use. It is used to treat various seizure types in patients with epilepsy.

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

Manufacturer / TM Owner

Zydus France

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Indications & Clinical Uses

Levetiracetam is an antiepileptic drug that reduces abnormal neuronal firing in the brain.

  • Partial seizures: helps control focal onset seizures and reduces their frequency.
  • Generalized tonic‑clonic seizures: provides seizure freedom or reduction in patients with primary generalized seizures.
  • Myoclonic seizures: diminishes rapid, involuntary 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 vesicle exocytosis, decreasing neuronal excitability and stabilising abnormal electrical activity that underlies seizure generation.

Side Effects

Levetiracetam may cause a range of adverse reactions, most of which are mild to moderate.

Common Side Effects

  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Somnolence: increased sleepiness or fatigue.
  • Headache: mild to moderate cranial pain.
  • Irritability: mood changes including agitation.
  • Nausea: upset stomach or feeling sick.
  • Fatigue: reduced energy levels.

Serious or Rare Side Effects

  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Mood disorders: depression, anxiety, or suicidal thoughts.
  • Allergic reactions: anaphylaxis, swelling of face or throat.
  • Blood dyscrasias: leukopenia, thrombocytopenia, or anemia.
  • Hepatic injury: elevated liver enzymes or hepatitis.
  • Respiratory depression: rare but potentially life‑threatening breathing difficulty.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for adverse events.

  • Renal impairment: assess kidney function and consider dose adjustment.
  • Hepatic dysfunction: monitor liver enzymes periodically.
  • Psychiatric history: watch for mood changes, depression, or suicidal ideation.
  • Concomitant CNS depressants: use caution as additive sedation may occur.
  • Pregnancy and lactation: weigh potential benefits against unknown risks; discuss with obstetric specialist.
  • Store below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Levetiracetam has a relatively low interaction profile, but certain drugs can alter its plasma levels.

Major Interactions (Avoid)

  • Strong enzyme inducers (e.g., carbamazepine, phenytoin, phenobarbital): may markedly reduce levetiracetam concentrations.
  • Concomitant use with other antiepileptics that lower seizure threshold: may increase risk of breakthrough seizures.

Moderate Interactions (Monitor Closely)

  • Alcohol: can enhance central nervous system depression and increase somnolence.
  • Sedative agents (e.g., benzodiazepines, opioids): may potentiate sedation and dizziness.
  • Antacids containing aluminum or magnesium: may slightly decrease absorption if taken simultaneously.

Frequently Asked Questions

Levetiracetam Zydus is prescribed to manage 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 by stabilising abnormal neuronal activity.

Levetiracetam binds to the synaptic vesicle protein SV2A, which regulates neurotransmitter release. This binding modulates vesicle exocytosis, leading to decreased neuronal excitability and preventing the rapid, uncontrolled firing that triggers seizures.

The appropriate dose of Levetiracetam Zydus is determined individually by the prescribing clinician based on the patient’s age, weight, renal function, and seizure type. Dosage adjustments are made according to therapeutic response and tolerability.

Safety data for levetiracetam in pregnancy and lactation are limited. The prescriber should evaluate the potential benefits against possible risks and discuss options with the patient. If used, close monitoring of both mother and infant is recommended.

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 pharmacokinetic profile with minimal protein binding and few drug‑drug interactions, distinguishing it from many enzyme‑inducing antiepileptics. It is often chosen for patients who need a well‑tolerated option with a rapid onset of action and convenient dosing.

Store Levetiracetam Zydus below 25 °C in its original container, protecting it from moisture, heat, and direct sunlight. Do not store in a bathroom or near a kitchen sink where humidity is high.

Levetiracetam Zydus is taken orally, usually with or without food, as directed by the prescriber. Tablets should be swallowed whole with water and not crushed or chewed unless specifically instructed.

Serious risks include severe skin reactions such as Stevens‑Johnson syndrome, mood disturbances like depression or suicidal thoughts, and rare blood disorders (e.g., leukopenia). Patients should seek immediate medical attention if they notice rash, mood changes, or signs of infection.

Patients with known hypersensitivity to levetiracetam or any of its excipients should avoid the product. Caution is also advised for individuals with severe renal impairment, uncontrolled psychiatric conditions, or those taking strong enzyme‑inducing antiepileptics without appropriate dose adjustments.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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