GNH USA

Europe — EMA

Keppra

GNH USA supplies Keppra (Levetiracetam), an anticonvulsant for partial, generalized tonic‑clonic and myoclonic seizures. Request a quote for global supply.

Levetiracetam

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What is Levetiracetam?

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

GNH USA supplies Keppra as a licensed, GDP‑compliant international pharmaceutical product, providing the medication to hospitals, pharmacies and clinics worldwide, with a focus on EU‑regulated markets and adhering to stringent quality standards.

What is Levetiracetam used for?

Levetiracetam (Keppra) is an anticonvulsant used in the management of epilepsy.

- Partial seizures: reduces frequency and severity of focal seizures. - Generalized tonic‑clonic seizures: helps prevent convulsive episodes. - Myoclonic seizures: decreases occurrence of sudden muscle jerks.

What are the side effects of Levetiracetam?

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

Common Side Effects: - Dizziness: transient sensation of light‑headedness. - Somnolence: increased sleepiness or fatigue. - Headache: mild to moderate cranial pain. - Nausea: occasional upset stomach. - Irritability: mood changes or agitation.

Serious or Rare Side Effects: - Severe skin reactions: rash, Stevens‑Johnson syndrome, or toxic epidermal necrolysis. - Psychiatric events: depression, suicidal thoughts, or aggressive behavior. - Hematologic abnormalities: low blood cell counts or anemia. - Respiratory depression: difficulty breathing, especially when combined with other CNS depressants.

What precautions apply to Levetiracetam?

When prescribing levetiracetam, clinicians should consider several precautionary measures to ensure safe use. - Renal impairment: assess kidney function and adjust therapy as needed. - Pregnancy: potential risks are not well defined; discuss benefits and alternatives with the patient. - Psychiatric symptoms: monitor for mood changes, depression, or suicidal ideation. - Concomitant CNS depressants: use caution as additive sedation may occur. - Discontinuation: avoid abrupt cessation; taper under medical supervision. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Levetiracetam interact with?

Levetiracetam has a relatively low interaction profile, but certain drug combinations require attention.

Major Interactions (Avoid): - Combined use with other antiepileptic drugs that significantly depress central nervous system activity (e.g., phenobarbital) may increase sedation and respiratory risk. - Co‑administration with drugs known to cause severe hypersensitivity reactions (e.g., lamotrigine) may heighten the risk of serious skin disorders.

Moderate Interactions (Monitor Closely): - Concurrent nephrotoxic agents (e.g., aminoglycosides) may exacerbate renal impairment; monitor kidney function. - Alcohol or other CNS depressants: may enhance drowsiness or dizziness. - Hormonal contraceptives: levetiracetam may reduce efficacy; consider alternative or additional contraceptive methods.

Frequently asked questions

What conditions is Keppra used to treat?+
Keppra, containing levetiracetam, is indicated for the treatment of several seizure types in epilepsy, including partial (focal) seizures, generalized tonic‑clonic seizures, and myoclonic seizures. It is prescribed to reduce the frequency and severity of these episodes in patients diagnosed with epilepsy.
How does levetiracetam work to control seizures?+
Levetiracetam exerts its antiepileptic effect by binding to the synaptic vesicle protein SV2A. This binding modulates the release of neurotransmitters, stabilizing neuronal firing and decreasing hyper‑excitability in the brain, which helps prevent the initiation and spread of seizure activity.
What determines the usual dose of Keppra?+
The appropriate dose of Keppra is individualized. A qualified prescriber determines the dosage based on factors such as the patient’s age, weight, renal function, seizure type, and response to therapy. Dosing recommendations are provided in the prescribing information, but the final regimen is set by the treating clinician.
Is Keppra safe to use during pregnancy or while breastfeeding?+
Safety data for levetiracetam during pregnancy and lactation are limited. The potential risks are not fully established, so the decision to use Keppra in pregnant or nursing women should be made after a careful risk‑benefit assessment by the healthcare provider.
How do I order Keppra from GNH USA?+
To request Keppra, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide. After the enquiry, the sales team will verify trade or institutional credentials, then provide pricing, availability, shipping details (including any cold‑chain requirements), and necessary import documentation.
How does Keppra compare with other antiepileptic drugs?+
Compared with older antiepileptics such as carbamazepine or valproate, levetiracetam has a simpler pharmacokinetic profile, fewer drug‑enzyme interactions, and does not require routine therapeutic drug monitoring. Its side‑effect spectrum is distinct, with a lower incidence of hepatic toxicity but a higher frequency of behavioral changes in some patients.
What are the recommended storage conditions for Keppra?+
Keppra intravenous solution should be stored at 2‑8 °C (refrigerated). Keep the product in its original packaging, protect it from light, and avoid freezing or shaking the vial, as these actions could compromise stability.
How is Keppra administered to patients?+
Keppra is supplied as an intravenous solution that is administered by slow infusion into a vein. The infusion rate and total daily volume are determined by the prescribing clinician, who may adjust the schedule based on the patient’s clinical response and renal function.
What are the most serious risks associated with Keppra?+
Serious adverse reactions to Keppra include severe skin disorders such as Stevens‑Johnson syndrome or toxic epidermal necrolysis, as well as psychiatric events like depression, suicidal thoughts, or aggressive behavior. Rare hematologic abnormalities and respiratory depression, particularly when combined with other central nervous system depressants, also warrant close monitoring.
Who should not use Keppra?+
Keppra should be avoided in individuals with a known hypersensitivity to levetiracetam or any component of the formulation. Patients with severe renal impairment may require alternative therapy or careful dose adjustment under specialist supervision. As always, the prescribing clinician assesses suitability on a case‑by‑case basis.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Levetiracetam
Route
Intravenous Use
Manufacturer
Ucb Pharma S.A.
Origin
EU

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