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

Levetiracetam Hospira

Active Ingredient:
Levetiracetam
Origin:
EU

Levetiracetam Hospira (Levetiracetam)

Levetiracetam, the active ingredient in Levetiracetam Hospira, is an anticonvulsant presented as an intravenous solution for intravenous use. It is employed to treat partial‑onset, generalized tonic‑clonic and myoclonic seizures in patients with epilepsy.

GNH India supplies Levetiracetam Hospira as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Pfizer Europe Ma Eeig

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Indications & Clinical Uses

Levetiracetam is an antiepileptic drug that modulates neuronal excitability in various seizure types.

  • Partial‑onset seizures: reduces seizure frequency and severity in focal epilepsy.
  • Generalized tonic‑clonic seizures: helps achieve seizure control in primary generalized epilepsy.
  • Myoclonic seizures: diminishes myoclonic jerks and improves daily functioning.

How It Works

  • Levetiracetam binds selectively to the synaptic vesicle protein SV2A, a key regulator of neurotransmitter release. This interaction modulates synaptic transmission, decreasing excessive neuronal firing and hyperexcitability that underlie epileptic seizures, without directly affecting ion channels or GABA receptors.

Side Effects

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

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Fatigue: generalized tiredness or lack of energy.
  • Somnolence: increased sleepiness, especially after dosing.
  • Headache: mild to moderate cranial pain.
  • Irritability: mood changes or increased agitation.
  • Nausea: occasional stomach upset.

Serious or Rare Side Effects

  • Severe allergic reactions: rash, swelling, or anaphylaxis.
  • Stevens‑Johnson syndrome: rare but serious skin disorder.
  • Blood dyscrasias: neutropenia or thrombocytopenia.
  • Suicidal thoughts: emergence of depressive or suicidal ideation.
  • Severe skin rash: toxic epidermal necrolysis.
  • Respiratory depression: marked breathing difficulty when combined with other CNS depressants.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety aspects.

  • Renal impairment: assess renal function and adjust monitoring as levetiracetam is renally excreted.
  • Hepatic impairment: use caution; liver disease may alter drug handling.
  • Pregnancy: risk category unknown; discuss potential benefits and risks with the patient.
  • Concomitant CNS depressants: monitor for enhanced sedation or respiratory effects.
  • Psychiatric symptoms: observe for mood changes, aggression, or depression.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Levetiracetam can interact with several medicines, requiring attention to dosage and monitoring.

Major Interactions (Avoid)

  • Strong enzyme inducers (e.g., carbamazepine, phenytoin): may lower levetiracetam plasma levels.
  • Alcohol: can increase central nervous system depression.
  • Valproate: potential additive toxicity, especially for hepatic function.

Moderate Interactions (Monitor Closely)

  • CNS depressants (benzodiazepines, opioids): monitor for excessive sedation.
  • Renal excretion inhibitors (e.g., probenecid): may raise levetiracetam concentrations.
  • Live vaccines: observe for altered immune response.

Frequently Asked Questions

Levetiracetam Hospira is an intravenous antiepileptic medication indicated for the treatment of partial‑onset, generalized tonic‑clonic, and myoclonic seizures in patients with epilepsy. It is administered when rapid seizure control is required or when oral therapy is not feasible.

Levetiracetam binds to the synaptic vesicle protein SV2A, which plays a crucial role in regulating neurotransmitter release. This binding modulates synaptic transmission, reducing excessive neuronal firing and stabilizing neuronal networks, thereby preventing seizure activity.

The dosage of Levetiracetam Hospira is individualized by the prescribing clinician based on the patient’s age, weight, renal function, and clinical response. Healthcare professionals determine the appropriate infusion rate and total daily amount according to established treatment guidelines.

The pregnancy safety category for levetiracetam is not definitively established. Clinicians should weigh potential benefits against unknown risks when prescribing to pregnant or nursing women, and discuss alternative options or close monitoring as 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 like carbamazepine or GABA‑enhancers such as phenobarbital. It generally has fewer drug‑enzyme interactions, a favorable tolerability profile, and can be used as add‑on therapy for refractory seizures.

Levetiracetam Hospira should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the solution in its original packaging until use to maintain stability and sterility.

The product is supplied as an intravenous solution and is administered by slow infusion into a vein, typically over 15 minutes to 30 minutes, under the supervision of qualified healthcare personnel. Infusion rates are adjusted according to the prescribed dose.

Serious risks include severe allergic reactions, Stevens‑Johnson syndrome, blood dyscrasias, suicidal ideation, and rare but life‑threatening skin conditions. Patients should be monitored for rash, mood changes, or signs of infection, and any concerning symptoms should prompt immediate medical evaluation.

Levetiracetam is contraindicated in individuals with known hypersensitivity to levetiracetam or any component of the formulation. Caution is advised for patients with severe renal impairment, uncontrolled psychiatric disorders, or those receiving interacting medications that could increase toxicity.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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