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 injectable solution for intravenous infusion. It is used as adjunctive therapy for various seizure types and for the intravenous treatment of status epilepticus in patients requiring rapid seizure control. It is indicated for partial‑onset, myoclonic, and primary generalized tonic‑clonic seizures, and is administered under medical supervision.

GNH India supplies Levetiracetam Hospira as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide. The company adheres to stringent quality standards and provides reliable global logistics for clinical use.

Manufacturer / TM Owner

Pfizer Europe Ma Eeig

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Indications & Clinical Uses

Levetiracetam is an anticonvulsant that targets seizure activity in the central nervous system.

  • Partial-onset seizures: Reduces frequency of focal seizures when used as add‑on therapy.
  • Myoclonic seizures: Decreases myoclonic jerks in patients with juvenile myoclonic epilepsy.
  • Primary generalized tonic‑clonic seizures: Lowers occurrence of generalized convulsive seizures as adjunctive treatment.
  • Status epilepticus: Provides rapid intravenous control of ongoing seizures unresponsive to first‑line agents.

How It Works

  • Levetiracetam binds to the synaptic vesicle protein SV2A, a key regulator of neurotransmitter release. This interaction modulates vesicle exocytosis, decreasing neuronal excitability and limiting the release of excitatory neurotransmitters such as glutamate. By stabilizing synaptic transmission, the drug helps prevent the abnormal electrical discharges that underlie epileptic seizures. The precise downstream pathways remain under investigation, but the overall effect is a reduction in hypersynchronous neuronal firing.

Side Effects

Levetiracetam may be associated with a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Dizziness: Sensation of light‑headedness or unsteadiness.
  • Fatigue: Generalized tiredness or lack of energy.
  • Nausea: Stomach upset often without vomiting.
  • Irritability: Mood changes or increased agitation.

Serious or Rare Side Effects

  • Severe allergic reaction: Rash, swelling, or anaphylaxis.
  • Mood or behavioral changes: Depression, suicidal thoughts, or aggression.
  • Blood abnormalities: Decreased white blood cells or platelets.
  • Respiratory depression: Marked slowing of breathing, especially with concomitant depressants.

Precautions & Warnings

When using Levetiracetam, clinicians should observe several precautionary measures to ensure patient safety.

  • Renal function: Adjust dosing in patients with impaired clearance.
  • Pregnancy: Use only if potential benefit justifies potential risk, as safety data are limited.
  • Concomitant CNS depressants: Monitor for additive sedation or respiratory effects.
  • Behavioral monitoring: Observe for new or worsening mood disturbances.
  • Discontinuation: Do not stop abruptly; taper under medical guidance to avoid seizure exacerbation.
  • Store at 2-8°C: Keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

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

Major Interactions (Avoid)

  • Carbamazepine: May reduce levetiracetam plasma levels, decreasing effectiveness.
  • Phenobarbital: Similar enzyme‑inducing effect that can lower levetiracetam concentrations.

Moderate Interactions (Monitor Closely)

  • Sedative agents (e.g., benzodiazepines, opioids): May enhance central nervous system depression.
  • Antidepressants (e.g., SSRIs): Potential for increased behavioral side effects.
  • Immunosuppressants (e.g., tacrolimus): Possible alteration of drug levels; monitor concentrations.

Frequently Asked Questions

Levetiracetam Hospira is an intravenous antiepileptic medication indicated as adjunctive therapy for partial‑onset, myoclonic and primary generalized tonic‑clonic seizures, and for the rapid treatment of status epilepticus when immediate seizure control is required.

Levetiracetam binds to the synaptic vesicle protein SV2A, modulating vesicle release and reducing neuronal excitability. This action limits the release of excitatory neurotransmitters, thereby decreasing the likelihood of abnormal electrical discharges that cause seizures.

The appropriate dose of Levetiracetam Hospira is determined by the prescribing clinician based on the patient’s age, weight, renal function, seizure type, and response to therapy. No fixed regimen is provided here; dosing must follow the prescriber’s order.

Safety data for levetiracetam during pregnancy are limited, and the drug is classified as having an unknown pregnancy category. It should be used only if the potential benefit justifies any potential risk to the fetus. Breastfeeding decisions should be made after consulting a healthcare professional.

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 (including cold‑chain where required) and necessary import documentation.

Levetiracetam has a unique mechanism targeting SV2A, which differs from sodium‑channel blockers like carbamazepine or GABA‑enhancers such as valproate. It is generally well tolerated, has few drug‑enzyme interactions, and can be administered intravenously, offering rapid control in acute settings compared with many oral agents.

The product must be stored at 2‑8 °C, protected from light, and should never be frozen or shaken. Keep the vials in the original packaging until use, and follow aseptic techniques during preparation and administration to maintain sterility.

Levetiracetam Hospira is given as an intravenous infusion. The infusion rate and total daily dose are prescribed by the treating physician, and the medication is typically diluted in compatible IV fluids before administration under clinical supervision.

Serious risks include severe allergic reactions such as anaphylaxis, significant mood or behavioral changes (including depression or suicidal thoughts), hematologic abnormalities like reduced white‑blood‑cell or platelet counts, and respiratory depression, especially when combined with other central nervous system depressants.

Patients with known hypersensitivity to levetiracetam or any component of the formulation should avoid its use. Caution is also advised in individuals with severe renal impairment, uncontrolled psychiatric conditions, or those receiving interacting enzyme‑inducing antiepileptic drugs without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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