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

Levetiracetam Teva

Active Ingredient:
Levetiracetam
Origin:
EU

Levetiracetam Teva (Levetiracetam)

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

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Levetiracetam is an antiepileptic medication that modulates neuronal excitability to control seizures.

  • Partial seizures: reduces frequency and severity of focal onset seizures.
  • Generalized tonic‑clonic seizures: helps prevent convulsive episodes.
  • Myoclonic seizures: decreases sudden muscle jerks.
  • Epilepsy (overall): contributes to overall seizure control across multiple seizure types.

How It Works

  • Levetiracetam binds to the synaptic vesicle protein SV2A, a key regulator of neurotransmitter release. This interaction modulates synaptic transmission, decreasing neuronal hyper‑excitability and stabilising abnormal electrical activity that underlies seizure generation.

Side Effects

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

Common Side Effects

  • Drowsiness: feeling unusually sleepy or fatigued.
  • Dizziness: sensation of light‑headedness or imbalance.
  • Headache: mild to moderate cranial pain.
  • Irritability: increased mood swings or agitation.
  • Nausea: feeling of stomach upset or urge to vomit.
  • Nasal congestion: blocked or runny nose.

Serious or Rare Side Effects

  • Severe allergic reaction: rash, swelling, or difficulty breathing.
  • Mood changes: depression, suicidal thoughts, or severe anxiety.
  • Blood disorders: low white blood cells or platelets.
  • Liver dysfunction: jaundice or elevated liver enzymes.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

Patients and healthcare providers should consider several safety measures when using Levetiracetam.

  • Renal impairment: adjust dose or monitor renal function.
  • Psychiatric history: monitor for mood changes or suicidal ideation.
  • Pregnancy: discuss potential risks with a healthcare professional.
  • Breastfeeding: evaluate benefits versus potential infant exposure.
  • Concomitant CNS depressants: use caution as additive sedation may occur.
  • Store at ambient temperature: keep below 25 °C, in original packaging, protected from moisture and direct sunlight.

Avoid Interactions

Levetiracetam may interact with other medicines, affecting efficacy or safety.

Major Interactions (Avoid)

  • Carbamazepine: may reduce levetiracetam plasma levels.
  • Phenobarbital: may lower levetiracetam concentrations.

Moderate Interactions (Monitor Closely)

  • Sedatives (e.g., benzodiazepines): may increase central nervous system depression.
  • Antidepressants (e.g., SSRIs): monitor for mood alterations.
  • Immunosuppressants (e.g., cyclosporine): observe for potential pharmacokinetic changes.
  • Hormonal contraceptives: efficacy generally unchanged, but advise standard precautions.

Frequently Asked Questions

Levetiracetam Teva is prescribed for the management of epilepsy, including partial (focal) seizures, generalized tonic‑clonic seizures, and myoclonic seizures. It helps reduce the frequency and severity of these seizure types in patients diagnosed with epilepsy.

Levetiracetam binds to the synaptic vesicle protein SV2A, which regulates neurotransmitter release. This binding modulates synaptic transmission, decreasing neuronal hyper‑excitability and stabilising abnormal electrical activity that can trigger seizures.

The appropriate dose of Levetiracetam Teva is determined by the prescribing clinician based on the patient’s age, weight, renal function, and seizure type. Dosage regimens are individualized and should follow the prescriber’s instructions.

The safety of levetiracetam during pregnancy and lactation has not been fully established. Healthcare providers should weigh potential benefits against possible risks and discuss alternative options when appropriate.

To request Levetiracetam Teva, 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 sodium‑channel blockers like carbamazepine or GABA‑enhancing agents such as valproate. It is generally well‑tolerated, has fewer drug‑enzyme interactions, and can be used as monotherapy or adjunct therapy depending on clinical needs.

Levetiracetam Teva tablets should be stored at ambient temperature, below 25 °C, in their original container. Protect them from moisture, excessive heat and direct sunlight to maintain product stability.

Levetiracetam Teva 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 advised.

Serious adverse reactions can include severe allergic responses (e.g., rash, swelling, breathing difficulty), significant mood changes such as depression or suicidal thoughts, and rare blood disorders. Patients should seek immediate medical attention if any of these symptoms occur.

Levetiracetam 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 conditions, or those taking interacting medications without proper monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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