Kedrovit® (Kedrovit®)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Active substanceAronia black fruit + Birch bud + Hawthorn fruit + Hawthorn flowers + Pine cedar Siberian walnut + [Honey]Aronia black fruit + Birch bud + Hawthorn fruit + Hawthorn flowers + Pine cedar Siberian walnut + [Honey]
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  • Kedrovit®
    elixir inwards 
    MELIGEN FP, CJSC     Russia
    • Dosage form: & nbspelixir
    Composition:

    1000 ml of the preparation contain:

    Active substances: pine cedar Siberian seed 54.0 g, hawthorn fruit 4.0 g, aronia black fruit, 2.0 g, birch kidney 1.5 g, eleutherococcus rhizomes and roots 1.0 g, hawthorn flowers 0.5 g.

    Excipients: honey natural 50.0 g, sucrose 22.7 g, ethyl alcohol 95% 421.0 g, water purified to 1000 ml.

    Description:The liquid is brown, with a specific smell. In the course of storage, precipitation may occur.
    Pharmacotherapeutic group:Generalizing agent of plant origin
    ATX: & nbsp

    A.13   Tetanus preparations

    Pharmacodynamics:

    It has a general strengthening effect, increases physical efficiency, promotes the regulation of metabolic processes in the body.

    Pharmacokinetics:

    The drug is a water-alcohol extract from a mixture of herbal medicinal raw materials and contains a complex of biologically active substances, and therefore, the conduct of pharmacokinetic studies is not possible.

    Indications:

    It is used for the treatment of asthenic-vegetative syndrome of various etiologies, in the period of recovery after the transferred diseases that occur with the defeat of parenchymal organs.

    Contraindications:Hypersensitivity to the components of the drug, including honey and bee products, acute cardiovascular and acute renal insufficiency, severe liver disease, alcoholism, craniocerebral trauma, brain disease, sugar deficiency / isomaltase, fructose intolerance, glucose-galactose malabsorption, age 18 years.
    Pregnancy and lactation:The use of the drug during pregnancy and during breastfeeding is contraindicated.
    Dosing and Administration:

    Inside for 2-3 teaspoons (10-15 ml), diluted in 100 ml of water. 2 times a day for 10-15 minutes before meals. The course of treatment is 5-7 days. If necessary, the course of treatment can be increased to 2-3 weeks after consulting a doctor.

    Shake before use.

    Side effects:

    Allergic reactions are possible. If, on the background of taking the drug, your condition worsens, and you notice any side effects not listed in this manual, contact your doctor.

    Overdose:

    When using the drug in doses exceeding the recommended, you may have a headache, nausea, vomiting. Treatment is symptomatic.

    Interaction:

    With simultaneous use with nicotinic acid, lipid-lowering agents (cholesterol absorption inhibitors, fibrates), an increase in hypolipidemic action is possible.

    If you are taking other medications, always consult a doctor before taking the drug.

    Special instructions:

    The composition of the drug contains sucrose, which should be taken into account by a patient with diabetes mellitus. The maximum single dose of the drug contains 0.34 g of sucrose (corresponding to 0.3 XE (bread units)), daily - 0.68 g (corresponding to 0.68 XE). The drug contains at least 37% of ethyl alcohol The maximum single dose of the drug contains 5.9 grams of absolute ethyl alcohol, the maximum daily dose of the drug contains 11.97 grams of absolute ethyl alcohol.

    Effect on the ability to drive transp. cf. and fur:

    Due to the presence of ethyl alcohol in the preparation, one should refrain from potentially dangerous activities requiring an increased concentration attention and speed of psychomotor reactions (management of vehicles, work with moving mechanisms, the work of a dispatcher, operator, etc.).

    Form release / dosage:

    Elixir.

    Packaging:

    100 ml, 250 ml in glass bottles with a screw neck. The bottles are sealed with hermetically sealed metal caps with gaskets and first opening control.

    One bottle together with instructions for use in a cardboard box. It is allowed to put the text of the instructions for use on the pack.
    Storage conditions:

    At a temperature of 15 to 25 ° C in a dark place.

    Keep out of the reach of children.

    Shelf life:

    3 years.

    Do not use after the expiration date.

    Terms of leave from pharmacies:Without recipe
    Registration number:LP-002613
    Date of registration:05.09.2014
    Expiration Date:05.09.2019
    The owner of the registration certificate:MELIGEN FP, CJSC MELIGEN FP, CJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp28.12.2017
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