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 anticonvulsant presented as an oral dosage form for oral use. It is prescribed to control partial, generalized tonic‑clonic and myoclonic seizures in patients with epilepsy, offering a broad spectrum of seizure management across adult and pediatric populations.

GNH India supplies Levetiracetam Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring consistent quality and regulatory compliance for global distribution.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Levetiracetam is an anticonvulsant that reduces neuronal excitability in various seizure types.

  • Partial seizures: helps achieve seizure control and lower seizure frequency.
  • Generalized tonic‑clonic seizures: contributes to complete seizure suppression and reduces recurrence.
  • Myoclonic seizures: diminishes rapid muscle jerks and improves overall seizure stability.

How It Works

  • Levetiracetam binds to the synaptic vesicle protein SV2A, modulating neurotransmitter release and stabilizing neuronal membranes. This interaction reduces excessive neuronal firing, thereby decreasing the likelihood of seizure propagation across the central nervous system.

Side Effects

Levetiracetam may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

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

Serious or Rare Side Effects

  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Suicidal thoughts: emergence of depressive or suicidal ideation.
  • Depression: new or worsening mood disorders.
  • Blood disorders: rare cases of leukopenia or thrombocytopenia.
  • Allergic reactions: anaphylaxis or angioedema.
  • Multi‑organ hypersensitivity: systemic inflammatory response.

Precautions & Warnings

Levetiracetam requires careful consideration of patient‑specific factors before initiation.

  • Renal impairment: assess kidney function and adjust dose if necessary.
  • Hepatic dysfunction: monitor liver enzymes and consider dose modification.
  • Psychiatric history: observe for mood changes, depression, or suicidal thoughts.
  • Concomitant CNS depressants: avoid excessive sedation when combined with other depressants.
  • Pregnancy and lactation: evaluate risk‑benefit ratio; use only if clearly needed.
  • Store below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Levetiracetam may interact with several medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Carbamazepine: enzyme induction may lower levetiracetam plasma levels.
  • Phenobarbital: may reduce seizure control by decreasing drug concentration.
  • Strong CYP3A4 inhibitors: can increase levetiracetam exposure.

Moderate Interactions (Monitor Closely)

  • Sedatives (e.g., benzodiazepines): may enhance central nervous system depression.
  • Hormonal contraceptives: levetiracetam may reduce contraceptive effectiveness.
  • Alcohol: combined use can intensify dizziness and drowsiness.

Frequently Asked Questions

Levetiracetam Stada is prescribed to treat epilepsy‑related seizure disorders, specifically partial seizures, generalized tonic‑clonic seizures, and myoclonic seizures. It helps reduce the frequency and severity of these seizures by stabilizing neuronal activity in the brain.

Levetiracetam binds to the synaptic vesicle protein SV2A, which modulates neurotransmitter release. This action dampens excessive neuronal firing, thereby lowering the likelihood of seizure initiation and spread across the central nervous system.

The appropriate dose of Levetiracetam Stada is determined individually by a qualified prescriber based on the patient’s age, weight, renal function, and seizure type. Dosage adjustments are made according to clinical response and tolerability.

Safety data for levetiracetam in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant. Healthcare providers should discuss individual risks and consider alternative therapies when appropriate.

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 broad spectrum of seizure control with a relatively favorable interaction profile compared with many enzyme‑inducing antiepileptics. Unlike some older agents, it does not require routine therapeutic drug monitoring, but individual response and tolerability still guide drug selection.

Levetiracetam Stada should be stored at temperatures below 25 °C, in its original container, protected from moisture and direct sunlight. Maintaining these conditions helps preserve the tablet’s potency and stability throughout its shelf life.

Levetiracetam Stada is taken orally, usually with or without food, as directed by the prescribing clinician. The tablets should be swallowed whole with water and not crushed or chewed unless specifically advised by a healthcare professional.

Serious risks include rare but severe skin reactions (e.g., Stevens‑Johnson syndrome), emergence of suicidal thoughts or depression, and hematologic abnormalities such as leukopenia. Patients should be monitored for any new or worsening psychiatric symptoms or skin changes.

Levetiracetam Stada is contraindicated in individuals with known hypersensitivity to levetiracetam or any of its excipients. Caution is also advised for patients with severe renal impairment who may require dose adjustments, and for those with a history of serious psychiatric disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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