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

Levetiracetam Tad

Active Ingredient:
Levetiracetam
Origin:
EU

Levetiracetam Tad (Levetiracetam)

Levetiracetam, the active ingredient in Levetiracetam Tad, is an antiepileptic presented as an oral tablet for oral use. It is employed to control various seizure types in patients diagnosed with epilepsy.
GNH India supplies Levetiracetam Tad as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Tad Pharma Gmbh

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Indications & Clinical Uses

Levetiracetam is an antiepileptic drug indicated for several seizure disorders.

  • Partial‑onset seizures: reduces frequency and severity of focal seizures.
  • Generalized tonic‑clonic seizures: helps prevent convulsive episodes.
  • Myoclonic seizures: diminishes sudden muscle jerks associated with this seizure type.

How It Works

  • Levetiracetam binds to the synaptic vesicle protein SV2A, modulating neurotransmitter release and stabilising neuronal membranes. This action reduces neuronal hyper‑excitability and limits the propagation of seizure activity across neural networks.

Side Effects

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

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Fatigue: increased tiredness or lack of energy.
  • Somnolence: excessive sleepiness.
  • Irritability: mood changes or agitation.
  • Headache: mild to moderate cranial pain.
  • Nausea: upset stomach or urge to vomit.

Serious or Rare Side Effects

  • Severe psychiatric reactions: depression, anxiety, or suicidal thoughts.
  • Stevens‑Johnson syndrome: rare skin blistering disorder.
  • Blood dyscrasias: anemia, leukopenia, or thrombocytopenia.
  • Hypersensitivity: rash, fever, or angioedema.
  • Rhabdomyolysis: muscle breakdown leading to renal impairment.
  • Hepatic injury: elevated liver enzymes or hepatitis.

Precautions & Warnings

When prescribing Levetiracetam, clinicians should consider several safety aspects.

  • Renal impairment: adjust dose in patients with reduced kidney function.
  • Psychiatric history: monitor for mood changes or suicidal ideation.
  • Discontinuation: avoid abrupt cessation to prevent seizure worsening.
  • Pregnancy: safety category unknown; weigh benefits against potential risks.
  • Elderly patients: start at lower dose and titrate cautiously.
  • Storage: Store at ambient temperature: keep below 25°C, retain in original container, protect from moisture.

Avoid Interactions

Levetiracetam can interact with other medicines that affect its plasma levels.

Major Interactions (Avoid)

  • Carbamazepine: enzyme induction may lower levetiracetam concentrations.
  • Phenytoin: may reduce levetiracetam efficacy through increased metabolism.
  • Phenobarbital: can decrease levetiracetam levels, risking seizure control.

Moderate Interactions (Monitor Closely)

  • Valproic acid: may increase levetiracetam exposure, requiring dose review.
  • Other antiepileptics (e.g., lamotrigine): monitor for additive side effects.
  • Oral contraceptives: levetiracetam may reduce hormonal efficacy, advise alternative contraception.

Frequently Asked Questions

Levetiracetam Tad is prescribed to treat several types of epilepsy, including partial‑onset seizures, generalized tonic‑clonic seizures, and myoclonic seizures. It helps reduce the frequency and intensity of seizure episodes in patients diagnosed with these conditions.

Levetiracetam binds to the synaptic vesicle protein SV2A, which modulates neurotransmitter release. By stabilising neuronal firing and decreasing excessive excitability, the drug limits the spread of seizure activity across the brain.

The specific dose of Levetiracetam Tad is determined by the prescribing clinician based on the patient’s age, weight, renal function, and seizure type. Dosage adjustments are made to achieve optimal seizure control while minimizing side effects.

Levetiracetam’s pregnancy safety category is not definitively established. Healthcare providers weigh potential benefits against unknown risks when prescribing to pregnant or nursing women. Consultation with a specialist is recommended before use in these populations.

To request Levetiracetam Tad, 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.

Compared with older agents such as carbamazepine or phenytoin, levetiracetam has a simpler pharmacokinetic profile, fewer drug‑enzyme interactions, and is generally well tolerated. However, individual response varies, and clinicians may choose therapy based on seizure type, comorbidities and patient preference.

Levetiracetam Tad 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 Tad is taken orally, usually with or without food, as directed by the prescriber. The tablets are swallowed whole with water and should be taken at the same times each day to maintain consistent blood levels.

Serious risks include severe psychiatric reactions such as depression or suicidal thoughts, rare skin disorders like Stevens‑Johnson syndrome, blood dyscrasias, and hypersensitivity reactions. Patients should report any unusual mood changes, rash, or signs of infection promptly.

Levetiracetam Tad is contraindicated in patients with known hypersensitivity to levetiracetam or any of its excipients. Caution is advised for individuals with severe renal impairment, uncontrolled psychiatric illness, or those who are pregnant without a clear benefit‑risk assessment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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