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

Levetiracetam Hikma

Active Ingredient:
Levetiracetam
Origin:
EU

Levetiracetam Hikma (Levetiracetam)

Levetiracetam, the active ingredient in Levetiracetam Hikma, is an anticonvulsant presented as an injectable solution for intravenous use. It treats partial seizures, generalized tonic‑clonic seizures and myoclonic seizures in patients with epilepsy, providing rapid plasma levels for acute management.

GNH India supplies Levetiracetam Hikma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring consistent quality and regulatory compliance across EU and global markets.

Manufacturer / TM Owner

Hikma Farmacêutica (Portugal), S.A.

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Indications & Clinical Uses

Levetiracetam is an antiepileptic medication used to control various seizure types.

  • Partial seizures: reduces the frequency of focal seizures in patients with epilepsy
  • Generalized tonic‑clonic seizures: helps prevent convulsive episodes in adults and children
  • Myoclonic seizures: decreases the occurrence of sudden muscle jerks associated with juvenile myoclonic epilepsy

How It Works

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

Side Effects

Levetiracetam may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Dizziness: mild to moderate sensation of light‑headedness
  • Fatigue: generalized tiredness or lack of energy
  • Somnolence: increased sleepiness or drowsiness
  • Headache: mild to moderate cranial pain
  • Irritability: mood changes or increased agitation
  • Nausea: upset stomach or feeling of queasiness

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction with rash, swelling, or breathing difficulty
  • Stevens‑Johnson syndrome: rare skin disorder with blistering and detachment
  • Blood dyscrasias: abnormal blood counts such as neutropenia or thrombocytopenia
  • Suicidal ideation: emergence of thoughts of self‑harm or depression
  • Severe skin rash: widespread rash that may progress to toxic epidermal necrolysis
  • Respiratory depression: marked reduction in breathing effort, especially with concomitant depressants

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for potential complications.

  • Renal impairment: adjust dose based on creatinine clearance and monitor renal function
  • Hepatic impairment: use with caution and observe for increased plasma concentrations
  • Pregnancy: limited data; prescribe only if potential benefit justifies potential risk to the fetus
  • Concomitant CNS depressants: may enhance sedation or respiratory depression; monitor closely
  • Behavioral changes: observe for mood swings, aggression, or suicidal thoughts during treatment
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake

Avoid Interactions

Levetiracetam has a low potential for drug‑drug interactions, but certain combinations require attention.

Major Interactions (Avoid)

  • Phenobarbital: may lower levetiracetam plasma levels, reducing efficacy
  • Carbamazepine: can decrease levetiracetam concentrations, potentially leading to breakthrough seizures

Moderate Interactions (Monitor Closely)

  • Other antiepileptic drugs: monitor seizure control and adjust doses as needed
  • Sedative agents (benzodiazepines, alcohol): may increase central nervous system depression
  • Renal excretion inhibitors (e.g., probenecid): may raise levetiracetam levels, requiring observation
  • Live vaccines: consider timing, as immunomodulation could affect vaccine response

Frequently Asked Questions

Levetiracetam Hikma is an intravenous antiepileptic drug indicated for the treatment of partial seizures, generalized tonic‑clonic seizures, and myoclonic seizures in patients with epilepsy. It is used both for acute seizure control and as part of long‑term management strategies.

Levetiracetam binds to the synaptic vesicle protein SV2A, which modulates neurotransmitter release. By stabilizing neuronal firing and reducing excitatory synaptic activity, it lowers the likelihood of seizure initiation and spread throughout the central nervous system.

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

Levetiracetam is classified as pregnancy category unknown; limited human data exist. It should be used during pregnancy only if the potential benefit justifies any potential risk to the fetus. Breastfeeding is not contraindicated, but the infant may be exposed through milk, so clinical judgment is required.

To order Levetiracetam Hikma, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details (including cold‑chain where applicable) and import documentation.

Compared with older agents such as valproate or carbamazepine, levetiracetam has a more favorable drug‑interaction profile and does not require routine therapeutic drug monitoring. It is often preferred for patients who need rapid intravenous administration or who have experienced adverse effects with enzyme‑inducing antiepileptics.

Levetiracetam Hikma should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the solution in its original container until use, and discard any product that appears discolored or contains particles.

Levetiracetam Hikma is given as an intravenous injection or infusion. The rate of administration is determined by the prescriber; rapid infusion may be used for acute seizure control, while slower infusion rates are employed for maintenance therapy. Administration should be performed by qualified healthcare personnel.

Serious risks include severe allergic reactions such as anaphylaxis, rare skin conditions like Stevens‑Johnson syndrome, blood dyscrasias, and emergence of suicidal thoughts or depressive symptoms. Patients should be monitored closely for any signs of these events, and treatment should be discontinued if they occur.

Levetiracetam is contraindicated in individuals with a known hypersensitivity to levetiracetam or any of its excipients. Caution is advised for patients with severe renal impairment who may require dose adjustment, and for those with a history of serious psychiatric disorders, as behavioral changes can be exacerbated.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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