Product image of Levetiracetam Ucb (Levetiracetam) supplied by GNH India

Levetiracetam Ucb

Active Ingredient:
Levetiracetam
Origin:
EU

Levetiracetam Ucb (Levetiracetam)

Levetiracetam, the active ingredient in Levetiracetam Ucb, is an anticonvulsant presented as an intravenous formulation for intravenous use. It is employed as adjunctive therapy for partial‑onset seizures and generalized tonic‑clonic seizures in patients with epilepsy.

GNH India supplies Levetiracetam Ucb as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Ucb Pharma Gmbh

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Indications & Clinical Uses

  • Levetiracetam is an antiepileptic drug that acts on seizure pathways to reduce abnormal neuronal firing.
  • Partial‑onset seizures: adjunctive therapy that lowers seizure frequency in patients with focal epilepsy.
  • Generalized tonic‑clonic seizures: adjunctive therapy that helps achieve better seizure control in patients with primary generalized epilepsy.
  • Epilepsy (broad): incorporated into overall seizure management strategies as part of combination therapy.

How It Works

  • Levetiracetam binds selectively to the synaptic vesicle protein SV2A, modulating neurotransmitter release and stabilizing neuronal excitability. This interaction reduces the propagation of abnormal electrical activity across synapses, thereby diminishing the likelihood of seizure generation without directly affecting ion channels or GABA receptors.

Side Effects

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

Common Side Effects

  • Dizziness or light‑headedness.
  • Fatigue or somnolence.
  • Headache.
  • Nausea or gastrointestinal discomfort.
  • Irritability or mood changes.
  • Nasal congestion or upper respiratory symptoms.

Serious or Rare Side Effects

  • Severe allergic reactions, including anaphylaxis.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Suicidal thoughts or behavior.
  • Severe skin rash or hypersensitivity.
  • Blood dyscrasias such as neutropenia or thrombocytopenia.
  • Hepatic dysfunction or elevated liver enzymes.

Precautions & Warnings

  • Before initiating therapy, clinicians should assess patient‑specific factors and monitor for potential risks.
  • Renal function: adjust dosing in patients with impaired renal clearance.
  • Psychiatric symptoms: monitor for mood changes, depression, or suicidal ideation.
  • Drug discontinuation: avoid abrupt cessation to prevent seizure exacerbation.
  • Pregnancy: risk category unknown; weigh benefits against potential fetal risks.
  • Drug interactions: review concomitant medications for possible pharmacokinetic effects.
  • Store at room temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Levetiracetam can interact with several medications, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Carbamazepine or phenytoin: may reduce levetiracetam plasma concentrations.
  • Enzyme‑inducing antiepileptics (e.g., phenobarbital): can lower drug exposure.
  • Concomitant use with other SV2A ligands: may increase risk of CNS depression.

Moderate Interactions (Monitor Closely)

  • Sedative agents (e.g., benzodiazepines, opioids): may enhance drowsiness.
  • Hormonal contraceptives: potential reduction in contraceptive effectiveness; advise alternative methods.

Frequently Asked Questions

Levetiracetam Ucb is an intravenous antiepileptic medication used as adjunctive therapy for partial‑onset seizures and generalized tonic‑clonic seizures in patients with epilepsy. It helps reduce seizure frequency when added to existing treatment regimens.

Levetiracetam binds to the synaptic vesicle protein SV2A, which modulates neurotransmitter release. This action stabilizes neuronal firing and reduces the spread of abnormal electrical activity that can trigger seizures.

The dosage of Levetiracetam Ucb is individualized and determined by the prescribing clinician based on the patient’s age, weight, renal function, and therapeutic response. No standard dose is provided here.

Levetiracetam’s pregnancy category is unknown, and safety data are limited. Clinicians should evaluate the potential benefits versus risks before prescribing to pregnant or breastfeeding women, and discuss alternative options 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 (including cold‑chain if needed), and import documentation.

Levetiracetam offers a distinct mechanism by targeting SV2A, which differs from sodium‑channel blockers or GABA‑enhancers. It generally has fewer drug‑enzyme interactions, a favorable tolerability profile, and does not require routine therapeutic drug monitoring, making it a convenient option for many patients.

Levetiracetam Ucb should be stored at room temperature, below 25 °C, in its original container. Keep the product protected from moisture and direct sunlight, and avoid freezing. Follow any additional handling instructions provided with the shipment.

Levetiracetam Ucb is administered intravenously by a healthcare professional. The infusion rate and duration are determined by the prescriber, typically based on the patient’s clinical condition and renal function.

Serious risks include severe allergic reactions such as anaphylaxis, life‑threatening skin conditions like Stevens‑Johnson syndrome, and psychiatric events including suicidal thoughts. Patients should be monitored closely for any signs of these reactions, and treatment should be discontinued if they occur.

Levetiracetam Ucb is contraindicated in patients with known hypersensitivity to levetiracetam or any of its excipients. Caution is advised for individuals with severe renal impairment, uncontrolled psychiatric disorders, or those who are pregnant without a clear benefit‑risk assessment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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