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  • Keppra oral solution 100 mg/ml, 300 ml— Made in Belgium — Free Delivery


    Brand: UCB Pharma S. A.
    Product Code: Keppra
    Availability: In Stock
    $71.54
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    Product description 

    Keppra oral solution is indicated as monotherapy (first choice) in the treatment of partial seizures with or without secondary generalization in adults and adolescents aged 16 years and over who are newly diagnosed with epilepsy.
    As an additional therapy in the treatment:
    • partial seizures with or without secondary generalization in adults and children older than 1 month with epilepsy;
    • myoclonic seizures in adults and adolescents over 12 years of age with juvenile myoclonic epilepsy;
    • primary generalized tonic-clonic seizures in adults and adolescents over 12 years of age with idiopathic generalized epilepsy.

    Compound

    Active ingredient: levetiracetam;
    1 ml of solution contains levetiracetam 100 mg;
    Excipients: citric acid monohydrate, ammonium glycyrrhizinate, sodium, methylparaben (E 218), propylparaben (E 216), glycerin 85% (E 422), liquid maltitol (E 965), potassium acesulfame (E 950), grape flavor Firmenich 501040A, purified water.

    Contraindications

    Hypersensitivity to levetiracetam or other pyrrolidone derivatives, as well as to any excipients of the preparation.

    Mode of application

    The preparation is taken orally, regardless of the meal. The oral solution can be taken after reconstitution in a glass of water or a feeding bottle. Levetiracetam may taste bitter after oral administration.

    Application features

    pregnant
    Pregnant women who receive treatment with levetiracetam should be provided with appropriate clinical follow-up.
    Children
    Keppra oral solution can be given to children from 1 month of age.
    Drivers
    Carefully.

    Overdose

    With an overdose of Keppra, drowsiness, agitation, aggression, respiratory depression, depression of consciousness, and coma were observed.
    In case of acute overdose, it is necessary to wash the stomach or induce vomiting. There is no specific antidote for levetiracetam. If necessary, carry out symptomatic treatment, including with the use of hemodialysis (60% of levetiracetam and 74% of the main metabolite are excreted).

    Side effects

    The most commonly reported adverse reactions were nasopharyngitis, drowsiness, headache, fatigue and dizziness.

    Interaction

    In some cases, a decrease in the effectiveness of levetiracetam has been reported with the simultaneous use of the osmotic laxative macrogol with oral levetiracetam. Therefore, macrogol should not be taken orally within one hour before and within one hour after taking levetiracetam.
    The degree of absorption of levetiracetam does not depend on food, but the absorption rate is slightly reduced when taken with food. There are no data on the interaction of levetiracetam with alcohol.

    Storage conditions

    Store in original packaging at temperatures not exceeding 25°C.
    Keep out of the reach of children.
    Shelf life - 3 years.

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