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

Levetiracetam Stada

Active Ingredient:
Levetiracetam
Origin:
EU

Levetiracetam Stada (Levetiracetam)

Levetiracetam, the active ingredient in Levetiracetam Stada, is an antiepileptic presented as an oral tablet for systemic use. It is indicated for the treatment of partial seizures, generalized tonic‑clonic seizures, and myoclonic seizures in both adult and pediatric patients requiring seizure control.

GNH India supplies Levetiracetam Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable sourcing for regulated markets and research institutions, ensuring consistent quality and compliance with EU standards through robust supply chain management.

Manufacturer / TM Owner

Laboratorio Stada, S.L.

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Indications & Clinical Uses

Levetiracetam is an antiepileptic medication that modulates neuronal excitability and is employed to control seizure activity across several seizure types in patients with epilepsy.

  • Partial seizures: reduces the frequency and severity of focal onset seizures in patients with epilepsy, improving quality of life.
  • Generalized tonic‑clonic seizures: helps prevent convulsive episodes and associated loss of consciousness in generalized seizure disorders, reducing injury risk.
  • Myoclonic seizures: decreases sudden, brief muscle jerks, improving control in myoclonic epilepsy, and supports daily functioning.

How It Works

  • Levetiracetam binds to the synaptic vesicle protein SV2A, a regulator of neurotransmitter release. This interaction modulates vesicle exocytosis, decreasing the release of excitatory neurotransmitters such as glutamate, and stabilizes neuronal membranes. The net effect is reduced neuronal hyper‑excitability, which underlies its anticonvulsant activity. It does not significantly affect GABAergic or sodium channel pathways, which contributes to its favorable drug‑interaction profile.

Side Effects

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

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Fatigue: feeling unusually tired or weak.
  • Headache: mild to moderate cranial pain.
  • Irritability: mood changes or increased agitation.
  • Nausea: upset stomach or feeling of queasiness.
  • Somnolence: increased sleepiness or drowsiness.
  • Coordination problems: unsteady gait or clumsiness.

Serious or Rare Side Effects

  • Severe allergic reaction: rash, swelling, or anaphylaxis.
  • Mood or behavior changes: depression, suicidal thoughts, or aggression.
  • Blood disorders: thrombocytopenia or leukopenia.
  • Stevens‑Johnson syndrome: rare severe skin reaction with blistering.

Precautions & Warnings

When prescribing Levetiracetam, clinicians should consider several precautionary measures to ensure safe use.

  • Renal function: adjust dose in patients with impaired renal clearance.
  • Psychiatric history: monitor for mood changes, depression, or suicidal ideation.
  • Pregnancy: use only if potential benefit justifies potential risk, as safety data are limited.
  • Concomitant CNS depressants: observe for additive sedation or dizziness.
  • Driving and machinery: advise patients to assess personal response before operating vehicles.
  • Store at ambient temperature: keep below 25 °C in original packaging, protect from moisture.

Avoid Interactions

Levetiracetam has a low potential for pharmacokinetic interactions, but certain drug combinations require attention.

Major Interactions (Avoid)

  • Carbamazepine: may reduce levetiracetam plasma levels, decreasing efficacy.
  • Phenobarbital: can lower levetiracetam concentrations, risking seizure breakthrough.

Moderate Interactions (Monitor Closely)

  • Alcohol: may enhance central nervous system depression, increasing dizziness or sedation.
  • Other antiepileptics (e.g., valproate, phenytoin): monitor seizure control as additive effects may occur.
  • Oral contraceptives: limited data suggest possible reduction in contraceptive effectiveness; advise additional contraceptive measures.

Frequently Asked Questions

Levetiracetam Stada is prescribed to treat epilepsy by reducing the frequency of partial seizures, generalized tonic‑clonic seizures, and myoclonic seizures. It is used in both adult and pediatric patients who require seizure control as part of a comprehensive antiepileptic regimen.

Levetiracetam binds to the synaptic vesicle protein SV2A, which regulates neurotransmitter release. This binding modulates vesicle exocytosis, lowering the release of excitatory neurotransmitters such as glutamate and stabilising neuronal membranes, thereby decreasing neuronal hyper‑excitability that leads to seizures.

The appropriate dose of Levetiracetam Stada is individualized by the prescribing clinician based on factors such as the patient’s age, weight, renal function, seizure type, and response to therapy. No fixed regimen is provided here; the prescriber sets the dosage.

Levetiracetam is classified with an unknown pregnancy category, meaning safety data are limited. It should only be used during pregnancy or lactation when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and under close medical supervision.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request verification of trade or institutional credentials before providing pricing, availability, shipping details and any necessary import documentation.

Compared with older antiepileptics such as carbamazepine or valproate, levetiracetam offers a simpler pharmacokinetic profile with fewer enzyme‑mediated drug interactions. It is generally well tolerated, does not require routine blood‑level monitoring, and can be used as monotherapy or adjunct therapy, though individual response varies.

Levetiracetam Stada tablets should be stored at ambient temperature, below 25 °C, in the original container to protect from moisture and light. Keep the product out of reach of children and avoid storing in areas with high humidity or extreme heat.

Levetiracetam Stada is taken orally as a tablet. It should be swallowed whole with water and can be taken with or without food. Patients should follow the dosing schedule prescribed by their healthcare professional and not alter the regimen without medical advice.

Serious risks include severe allergic reactions such as rash, swelling, or anaphylaxis; significant mood or behavioral changes including depression, suicidal thoughts, or aggression; and rare blood disorders like thrombocytopenia or leukopenia. Any of these symptoms require immediate medical attention.

Patients with a known hypersensitivity to levetiracetam or any component of the tablet should avoid its use. Individuals with severe renal impairment must have dose adjustments and close monitoring; otherwise, the medication may be contraindicated. Consultation with a healthcare provider is essential before starting therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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