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

Levetiracetam Stada Arzneimittel

Active Ingredient:
Levetiracetam
Origin:
EU

Levetiracetam Stada Arzneimittel (Levetiracetam)

Levetiracetam, the active ingredient in Levetiracetam Stada Arzneimittel, is an antiepileptic presented as an oral tablet for oral use. It treats partial‑onset, generalized tonic‑clonic and myoclonic seizures in patients with epilepsy.

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

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

  • Levetiracetam is an antiepileptic drug indicated for several seizure types.
  • Partial‑onset seizures: reduces the frequency of focal seizure episodes.
  • Generalized tonic‑clonic seizures: helps prevent bilateral convulsive episodes.
  • Myoclonic seizures: decreases the occurrence of rapid, involuntary muscle jerks.

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 the central nervous system.

Side Effects

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

Common Side Effects

  • Dizziness
  • Somnolence
  • Fatigue
  • Headache
  • Irritability
  • Nausea

Serious or Rare Side Effects

  • Severe allergic reactions such as anaphylaxis
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis
  • Blood dyscrasias including neutropenia or thrombocytopenia
  • Suicidal thoughts or behavior
  • Severe depression or mood changes
  • Rash with systemic involvement

Precautions & Warnings

  • Before initiating therapy, consider the following safety measures.
  • Renal impairment: adjust dose according to renal function.
  • Hepatic impairment: monitor liver enzymes regularly.
  • Pregnancy: discuss potential risks with a healthcare professional.
  • Psychiatric symptoms: observe for mood changes, depression, or suicidal ideation.
  • Concomitant CNS depressants: use with caution as additive sedation may occur.
  • Store at below 25°C: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Levetiracetam can interact with other medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • Alcohol: can enhance central nervous system depression.
  • Other antiepileptic drugs: may necessitate dose adjustments.
  • Renal excretion inhibitors: monitor renal function and consider dose modification.

Frequently Asked Questions

Levetiracetam Stada Arzneimittel is prescribed to manage epilepsy. It is indicated for partial‑onset seizures, generalized tonic‑clonic seizures, and myoclonic seizures, helping to lower the frequency and severity of seizure episodes in patients diagnosed with these seizure types.

Levetiracetam binds selectively to the synaptic vesicle protein SV2A in the brain. This binding modulates neurotransmitter release, stabilises neuronal firing, and reduces hyper‑excitability, thereby decreasing the likelihood of seizure propagation.

The specific dose of levetiracetam is individualized by the prescribing clinician based on factors such as the patient’s age, weight, renal function, and seizure type. Dosage regimens are not standardized and should follow the prescriber’s instructions.

Safety data for levetiracetam in pregnancy and lactation are limited. Healthcare providers should weigh potential benefits against possible risks and discuss these considerations with the patient. Breastfeeding decisions should also be made in consultation with a medical professional.

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.

Compared with older agents such as carbamazepine or valproate, levetiracetam has a relatively simple pharmacokinetic profile, fewer drug‑enzyme interactions, and is generally well tolerated. However, individual response varies, and the choice of therapy depends on seizure type, comorbidities and patient‑specific factors.

Levetiracetam tablets should be stored at temperatures below 25 °C in their original container, protected from moisture and direct sunlight. Keep the product out of reach of children and avoid exposing it to excessive heat or humidity.

Levetiracetam 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 the formulation specifically allows it.

Serious adverse events include severe allergic reactions (e.g., anaphylaxis), skin disorders such as Stevens‑Johnson syndrome, blood dyscrasias, and psychiatric effects like depression, mood changes, or suicidal thoughts. Prompt medical attention is required if any of these occur.

Levetiracetam is contraindicated in individuals with a known hypersensitivity to the drug or any of its excipients. Patients with severe renal impairment may require special dosing considerations, and clinicians should evaluate suitability on a case‑by‑case basis.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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