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 oral use. It is employed to control various seizure types in patients with epilepsy.
GNH India supplies Levetiracetam Stada 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 that reduces abnormal neuronal firing in the brain.

  • Epilepsy: helps achieve seizure control across multiple seizure types.
  • Partial‑onset seizures: reduces frequency and severity of focal seizures.
  • Generalized tonic‑clonic seizures: lowers the occurrence of convulsive episodes.

How It Works

  • Levetiracetam binds to the synaptic vesicle protein SV2A, modulating neurotransmitter release and decreasing neuronal excitability. This interaction stabilizes synaptic transmission and diminishes the propagation of epileptiform activity without directly affecting ion channels or GABA receptors.

Side Effects

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

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Fatigue: feeling unusually tired or low in energy.
  • Headache: mild to moderate pain in the head region.
  • Nausea: occasional upset stomach or urge to vomit.
  • Irritability: changes in mood or increased agitation.
  • Somnolence: tendency to feel sleepy during the day.

Serious or Rare Side Effects

  • Severe allergic reaction: rash, swelling, or difficulty breathing.
  • Mood changes: depression, suicidal thoughts, or aggressive behavior.
  • Blood disorders: low white blood cells or platelets.
  • Hepatic dysfunction: signs of liver injury such as jaundice.
  • Stevens‑Johnson syndrome: severe skin blistering.
  • Multi‑organ hypersensitivity: systemic inflammatory response.

Precautions & Warnings

Before initiating therapy, consider the following safety measures.

  • Renal function: adjust dose if creatinine clearance is reduced.
  • Psychiatric history: monitor for mood alterations or suicidal ideation.
  • Concomitant CNS depressants: assess additive sedation risk.
  • Pregnancy: discuss potential risks with a healthcare professional.
  • Lactation: evaluate benefits versus possible infant exposure.
  • Storage: Store below 25°C: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Carbamazepine: may lower levetiracetam plasma levels, reducing seizure control.
  • Phenobarbital: can decrease levetiracetam exposure, necessitating dose adjustment.

Moderate Interactions (Monitor Closely)

  • Valproic acid: may increase levetiracetam concentrations, watch for side effects.
  • Oral contraceptives: levetiracetam may reduce hormonal efficacy, consider alternative contraception.
  • Antidepressants (SSRIs): monitor for additive central nervous system effects.
  • Immunosuppressants (e.g., cyclosporine): observe for altered drug levels.
  • Alcohol: increased sedation and dizziness may occur.

Frequently Asked Questions

Levetiracetam Stada is used to treat epilepsy, including partial‑onset seizures and generalized tonic‑clonic seizures. It helps reduce the frequency and severity of seizures by stabilizing neuronal activity in the brain.

Levetiracetam binds to the synaptic vesicle protein SV2A, which modulates neurotransmitter release. This action decreases neuronal excitability and limits the spread of abnormal electrical activity that leads to seizures.

The dose of Levetiracetam Stada is individualized by the prescribing clinician based on the patient’s age, weight, renal function, and seizure type. Only a qualified healthcare professional should determine the appropriate dosing regimen.

Safety data for levetiracetam in pregnancy and lactation are limited. Women who are pregnant, planning pregnancy, or breastfeeding should discuss potential risks and benefits with their healthcare provider before using the medication.

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 distinct mechanism by targeting SV2A, which differs from sodium‑channel blockers or GABA‑enhancing agents. It generally has fewer drug‑enzyme interactions, a favorable tolerability profile, and can be used as monotherapy or adjunctive therapy, making it a versatile option in epilepsy management.

Levetiracetam Stada tablets should be stored below 25 °C in their original packaging, protected from moisture and direct sunlight. Keep the product out of reach of children and avoid exposure to extreme temperatures.

Levetiracetam Stada is taken orally, usually with or without food, as directed by the prescriber. The tablets should be swallowed whole with water and not crushed or chewed unless specifically instructed.

Serious risks include severe allergic reactions, mood changes such as depression or suicidal thoughts, and rare blood disorders. Patients should seek immediate medical attention if they experience rash, swelling, difficulty breathing, or significant mood alterations.

Individuals with known hypersensitivity to levetiracetam or any of its excipients should avoid the product. Caution is also advised for patients 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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