Product image of Kepricet (Levetiracetam) supplied by GNH India

Kepricet

Active Ingredient:
Levetiracetam
Origin:
EU

Kepricet (Levetiracetam)

Levetiracetam, the active ingredient in Kepricet, is a Antiepileptic presented as an oral dosage form for Oral use. It is used to treat various seizure types in patients with epilepsy.
GNH India supplies Kepricet as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Pharmazac Sa

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Indications & Clinical Uses

Kepricet, an antiepileptic drug, is employed in the management of seizure disorders.

  • Epilepsy: reduces the frequency and severity of seizures across the epilepsy spectrum.
  • Partial seizures: controls focal onset seizures that originate in a specific brain region.
  • Generalized seizures: helps prevent tonic‑clonic and other generalized seizure types.

How It Works

  • Levetiracetam modulates the synaptic vesicle protein SV2A, which plays a key role in neurotransmitter release. By binding to SV2A, the drug stabilizes neuronal membranes and reduces hyper‑excitability, thereby decreasing the likelihood of seizure propagation throughout the central nervous system.

Side Effects

Levetiracetam may cause a range of adverse reactions, which vary in frequency and severity.

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Fatigue: feeling unusually tired or lacking energy.
  • Somnolence: increased sleepiness during the day.
  • Headache: mild to moderate cranial pain.
  • Irritability: mood changes or increased agitation.
  • Nausea: upset stomach or urge to vomit.

Serious or Rare Side Effects

  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Depression or suicidal thoughts: mood disturbances requiring immediate attention.
  • Blood disorders: including leukopenia or thrombocytopenia.
  • Multi‑organ hypersensitivity: systemic allergic response.
  • Severe allergic reactions: anaphylaxis or angioedema.
  • Hepatic injury: rare liver function abnormalities.

Precautions & Warnings

When prescribing or dispensing Kepricet, several safety considerations should be observed.

  • Renal impairment: assess kidney function and adjust dose if necessary.
  • Hepatic impairment: monitor liver enzymes and consider dose modification.
  • Pregnancy: potential risks are unknown; use only if benefits outweigh risks.
  • Concomitant CNS depressants: may enhance sedation and impair coordination.
  • Driving or operating machinery: caution advised due to possible dizziness or drowsiness.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Carbamazepine: induces metabolism, reducing levetiracetam levels.
  • Phenytoin: increases hepatic enzyme activity, lowering drug concentration.
  • Rifampin: strong enzyme inducer that may decrease therapeutic effect.

Moderate Interactions (Monitor Closely)

  • Valproic acid: may raise levetiracetam plasma levels.
  • Alcohol: can intensify central nervous system depression.
  • Oral contraceptives: levetiracetam may reduce hormonal efficacy, requiring additional contraceptive measures.

Frequently Asked Questions

Kepricet contains levetiracetam, an antiepileptic medication prescribed to control various types of seizures, including partial (focal) seizures and generalized tonic‑clonic seizures in patients diagnosed with epilepsy.

Levetiracetam binds to the synaptic vesicle protein SV2A, modulating neurotransmitter release and stabilizing neuronal firing. This action reduces excessive neuronal excitability, helping to prevent the initiation and spread of seizure activity.

The dosage of Kepricet is individualized by the prescribing clinician based on the patient’s age, weight, renal function, and seizure type. Only a qualified healthcare professional should determine the appropriate regimen.

Safety data for levetiracetam in pregnancy and lactation are limited. It should be used only if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and under close medical supervision.

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 and import documentation.

Compared with older agents such as carbamazepine or phenytoin, levetiracetam has a more favorable drug‑interaction profile and does not require routine therapeutic drug monitoring, though individual response and tolerability may vary.

Kepricet should be stored at room temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and do not use after the expiry date.

Kepricet is taken orally, usually with or without food, as directed by the prescribing physician. Tablets (or the appropriate oral dosage form) should be swallowed whole with a glass of water.

Serious adverse events include severe skin reactions (e.g., Stevens‑Johnson syndrome), mood changes such as depression or suicidal ideation, and rare blood disorders. Patients should seek immediate medical attention if they notice any of these symptoms.

Kepricet is contraindicated in patients with known hypersensitivity to levetiracetam or any of its excipients. Caution is also advised for individuals with severe renal impairment, as dose adjustment may be required.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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