Product image of Keppra (Levetiracetam) supplied by GNH India

Keppra

Active Ingredient:
Levetiracetam
Origin:
EU

Keppra (Levetiracetam)

Levetiracetam, the active ingredient in Keppra, is an anticonvulsant presented as an oral tablet for oral use and marketed throughout the European Union. It is prescribed to control partial, generalized tonic‑clonic and myoclonic seizures in patients diagnosed with epilepsy, helping to reduce seizure frequency and improve quality of life.

GNH India supplies Keppra as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, transplant centres and oncology centres across worldwide, ensuring reliable sourcing and regulatory compliance for global health partners.

Manufacturer / TM Owner

Ucb Pharma S.A.

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Indications & Clinical Uses

Levetiracetam is an anticonvulsant that targets neuronal excitability in epilepsy.

  • Partial seizures: Reduces frequency and severity of focal onset seizures.
  • Generalized tonic-clonic seizures: Helps prevent convulsive episodes in patients with generalized epilepsy.
  • Myoclonic seizures: Controls rapid, brief muscle jerks associated with myoclonic epilepsy.

How It Works

  • Levetiracetam binds to the synaptic vesicle protein SV2A, a key regulator of neurotransmitter release. This interaction modulates calcium‑dependent exocytosis, decreasing neuronal hyper‑excitability and stabilizing synaptic transmission. By reducing the release of excitatory neurotransmitters, the drug lowers the likelihood of seizure initiation without directly affecting ion channels or GABA receptors. It does not significantly bind to other receptor systems, contributing to its relatively selective profile.

Side Effects

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

Common Side Effects

  • Dizziness: Sensation of light‑headedness or unsteadiness.
  • Fatigue: Generalized tiredness or lack of energy.
  • Somnolence: Increased sleepiness or drowsiness.
  • Headache: Mild to moderate cranial pain.
  • Irritability: Mood changes including agitation.
  • Nausea: Stomach upset or feeling sick.

Serious or Rare Side Effects

  • Severe allergic reaction: Rash, swelling, or difficulty breathing.
  • Stevens‑Johnson syndrome: Rare skin disorder with blistering.
  • Suicidal thoughts: New or worsening depressive symptoms.
  • Severe depression: Persistent low mood affecting daily function.
  • Blood disorders: Low white blood cells or platelets.
  • Liver injury: Elevated enzymes indicating hepatic stress.

Precautions & Warnings

When prescribing levetiracetam, clinicians should consider several safety measures to minimize risk.

  • Renal function: Assess and adjust dose in patients with impaired kidney function.
  • Psychiatric history: Monitor for mood changes, depression or suicidal ideation.
  • Discontinuation: Avoid abrupt cessation; taper gradually under medical supervision.
  • Drug interactions: Review concomitant medications that may alter levetiracetam levels.
  • Pregnancy: Use only if potential benefit justifies potential risk; data limited.
  • Store at room temperature: Keep in original packaging, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Carbamazepine: Increases metabolism, reducing levetiracetam plasma concentrations.
  • Phenytoin: Induces hepatic enzymes, leading to lower drug levels.
  • Rifampin: Strong enzyme inducer that markedly decreases levetiracetam exposure.

Moderate Interactions (Monitor Closely)

  • Valproic acid: May increase levetiracetam concentrations, requiring dose adjustment.
  • CNS depressants: Additive sedation when combined with alcohol or other sedatives.

Frequently Asked Questions

Keppra, containing levetiracetam, is prescribed to treat epilepsy by controlling partial, generalized tonic‑clonic and myoclonic seizures. It helps reduce seizure frequency and improve quality of life for patients with various seizure types.

Levetiracetam binds to the synaptic vesicle protein SV2A, modulating neurotransmitter release and decreasing neuronal hyper‑excitability. This action stabilizes synaptic transmission and lowers the likelihood of seizure initiation without directly affecting ion channels.

The dosage of Keppra is individualized; a qualified prescriber determines the appropriate amount based on the patient’s age, weight, renal function and seizure type. Patients should follow the prescribing physician’s instructions and not adjust the dose on their own.

Safety data for levetiracetam in pregnancy and lactation are limited. Use is generally reserved for situations where the potential benefit outweighs any possible risk to the fetus or infant, and decisions should be made in consultation with a healthcare professional.

To request Keppra, 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 and necessary import documentation.

Compared with older anticonvulsants such as carbamazepine or phenytoin, levetiracetam offers a distinct mechanism via SV2A binding, a relatively favorable side‑effect profile, and fewer drug‑enzyme interactions, making it a common alternative for patients who need a well‑tolerated regimen.

Keppra tablets should be stored at room temperature, below 25 °C, in the original container to protect them from moisture and light. Keep the medication out of reach of children and do not use after the expiration date.

Keppra is taken orally, usually with or without food, as directed by the prescribing clinician. The tablets are swallowed whole with a glass of water, and the dosing schedule (once, twice or thrice daily) is based on individual therapeutic needs.

The most serious risks include severe allergic reactions such as Stevens‑Johnson syndrome, emergent suicidal thoughts or depression, and rare blood disorders. Patients should seek immediate medical attention if they experience rash, mood changes, or signs of infection.

Keppra is contraindicated in individuals with known hypersensitivity to levetiracetam or any of its excipients. Caution is also advised for patients with severe renal impairment, uncontrolled psychiatric conditions, or those taking interacting enzyme‑inducing drugs without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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