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 a tablet for oral use. It treats partial seizures, generalized tonic‑clonic seizures and myoclonic seizures 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 used in the management of epilepsy and related seizure disorders.
  • Partial seizures: reduces the frequency of focal onset seizures in patients with epilepsy.
  • Generalized tonic‑clonic seizures: helps control convulsive episodes in generalized epilepsy.
  • Myoclonic seizures: decreases the occurrence of brief, shock‑like muscle jerks in patients with myoclonic epilepsy.

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 suppresses the propagation of seizure activity across the central nervous system.

Side Effects

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

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Fatigue: feeling unusually tired or low in energy.
  • Headache: mild to moderate head pain.
  • Irritability: increased mood lability.
  • Nausea: occasional upset stomach.
  • Somnolence: drowsiness or sleepiness.

Serious or Rare Side Effects

  • Severe allergic reaction: rash, swelling, or breathing difficulty.
  • Mood changes: depression or suicidal thoughts.
  • Stevens‑Johnson syndrome: severe skin blistering.
  • Blood dyscrasias: abnormal blood counts.
  • Hepatic dysfunction: elevated liver enzymes.
  • Severe skin reactions: toxic epidermal necrolysis.

Precautions & Warnings

  • Before prescribing Levetiracetam, clinicians should consider patient‑specific factors and monitor for potential risks.
  • Renal impairment: adjust dose based on renal function.
  • Pregnancy: evaluate risk‑benefit as safety data are limited.
  • Psychiatric history: monitor for mood alterations.
  • Concomitant CNS depressants: observe for additive sedation.
  • Elderly patients: start at lower dose and titrate cautiously.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Carbamazepine: may lower levetiracetam plasma levels.
  • Phenobarbital: may reduce seizure control.
  • Phenytoin: potential decrease in levetiracetam exposure.

Moderate Interactions (Monitor Closely)

  • Alcohol: may enhance central nervous system depression.
  • Other antiepileptics (e.g., valproate, lamotrigine): monitor seizure control and side‑effect profile.
  • Oral contraceptives: limited data, observe for hormonal changes.

Frequently Asked Questions

Levetiracetam Stada is prescribed to manage epilepsy, specifically to reduce the frequency of partial seizures, generalized tonic‑clonic seizures, and myoclonic seizures in patients diagnosed with seizure disorders.

Levetiracetam binds to the synaptic vesicle protein SV2A, which modulates neurotransmitter release and stabilises neuronal firing. This reduces excessive neuronal excitability, helping to prevent the initiation and spread of seizure activity.

The appropriate dose of Levetiracetam Stada is determined by the prescribing clinician based on the patient’s age, weight, renal function, and seizure type. Dosage adjustments are individualized and should follow the prescriber’s instructions.

Safety data for levetiracetam in pregnancy and lactation are limited. Clinicians should weigh the potential benefits against possible risks and discuss options with the patient. Breastfeeding decisions should also be made in consultation with a healthcare 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.

Levetiracetam offers a distinct mechanism by targeting SV2A, which differs from sodium‑channel blockers like carbamazepine or GABA‑enhancing agents such as valproate. It is generally well‑tolerated, has few drug‑enzyme interactions, and may be preferred when minimizing metabolic drug‑drug interactions is important.

Levetiracetam Stada tablets should be stored at ambient temperature, below 25 °C, in the original packaging to protect from moisture and light. Keep the product out of reach of children and do not use if the packaging is damaged.

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 chewed or crushed unless specifically instructed.

Serious risks include severe allergic reactions (e.g., Stevens‑Johnson syndrome), mood changes such as depression or suicidal thoughts, and rare blood disorders. Patients should seek immediate medical attention if they experience rash, swelling, mood disturbances, or unusual bleeding.

Levetiracetam Stada is contraindicated in patients with known hypersensitivity to levetiracetam or any of the tablet’s excipients. Caution is also advised for individuals with severe renal impairment who have not had dose adjustments, and for those with a history of serious psychiatric reactions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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