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 employed to control various types of epileptic seizures in patients requiring seizure management.

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 modulates neuronal excitability to reduce seizure activity.

  • Partial seizures: helps achieve seizure freedom or reduction in frequency.
  • Generalized tonic‑clonic seizures: contributes to control of convulsive episodes.
  • Myoclonic seizures: assists in decreasing rapid, involuntary muscle jerks.

How It Works

  • Levetiracetam binds to the synaptic vesicle protein SV2A, a key regulator of neurotransmitter release. This interaction modulates synaptic transmission, reducing neuronal hyper‑excitability and stabilising neuronal firing patterns, which underlies its anticonvulsant effect in various seizure types.

Side Effects

Levetiracetam may cause a range of adverse reactions, most of which are mild to moderate in severity.

Common Side Effects

  • Drowsiness: feeling unusually sleepy or fatigued.
  • Dizziness: sensation of light‑headedness or unsteadiness.
  • 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 aggressive behavior.
  • Blood disorders: signs of anemia or low platelet count.
  • Liver function abnormalities: elevated liver enzymes.
  • Skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

Before initiating therapy, consider patient‑specific factors and monitor for potential risks.

  • Renal impairment: adjust dosing based on kidney function.
  • Hepatic disease: use with caution; monitor liver enzymes.
  • Psychiatric history: observe for mood alterations or suicidal ideation.
  • Concomitant CNS depressants: may enhance sedation.
  • Pregnancy and lactation: evaluate risk‑benefit ratio with prescriber.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • Alcohol: may increase central nervous system depression.
  • Sedative antihistamines: can enhance drowsiness.
  • Other antiepileptics (e.g., valproate): monitor for additive side effects.
  • Oral contraceptives: possible reduction in hormonal efficacy.
  • Immunosuppressants: observe for altered drug levels.

Frequently Asked Questions

Levetiracetam Stada is used to treat various types of epileptic seizures, including partial seizures, generalized tonic‑clonic seizures, and myoclonic seizures. It helps reduce the frequency and severity of seizure episodes in patients diagnosed with epilepsy.

Levetiracetam binds to the synaptic vesicle protein SV2A, which plays a crucial role in neurotransmitter release. By modulating this protein, the drug stabilises neuronal firing and decreases excessive neuronal excitability, thereby preventing seizure activity.

The appropriate dose of Levetiracetam Stada is determined by the prescribing healthcare professional based on the patient’s age, weight, renal function, and seizure type. Dosage adjustments are made individually to achieve optimal seizure control.

Safety of levetiracetam during pregnancy or lactation has not been fully established. Prescribers weigh potential benefits against possible risks, and women who are pregnant, planning pregnancy, or breastfeeding should discuss treatment options with their healthcare provider.

To 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 like carbamazepine or GABA‑enhancing agents such as valproate. It generally has fewer drug‑enzyme interactions, but individual response and tolerability vary, so clinicians choose based on patient profile.

Store Levetiracetam Stada at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture and direct sunlight to maintain stability throughout its shelf life.

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

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

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 medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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