Active substanceLevomenthol solution in menthil isovalerateLevomenthol solution in menthil isovalerate
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  • Dosage form: & nbspsublingual tablets
    Composition:

    1 tablet contains:

    active substance: levomenthol solution in menthyl isovalerate (validol) 0.06 g;

    Excipients: dextrose (glucose) monohydrate 0.188 g; sucrose (sugar) 0.511 g; calcium stearate 0.008 g; povidone (polyvinylpyrrolidone) 0.007 g; silicon dioxide colloid (aerosil) 0.016 g; Potato starch 0.010 g.

    Description:Tablets are flat-cylindrical white or white with grayish patches of color, with a characteristic smell of menthol.
    Pharmacotherapeutic group:Coronarodilating agent of reflex action
    ATX: & nbsp

    C.01.E.X   Other combination drugs for the treatment of heart disease

    Pharmacodynamics:

    Has a sedative effect, has a moderate reflex vasodilator effect due to irritation of sensitive nerve endings. It stimulates the production and release of enkephalins, endorphins and a number of other peptides, kinins (due to irritation of the receptors of the oral mucosa), which take an active part in the regulation of vascular permeability, the formation of pain. Dextrose (glucose) is involved in various metabolic processes in the body, enhances oxidation-reduction processes in the body. When taken under the tongue, the therapeutic effect, on average, comes in 5 minutes, while up to 70% of the drug is released within 3 minutes.

    Pharmacokinetics:When received under the tongue levomenthol and menthylizovalerate are absorbed from the mucous membrane of the oral cavity.After absorption, they are metabolized in the liver and excreted by the kidneys in the form of glucuronides.
    Indications:

    Functional cardialgia, neuroses, and also as an antiemetic for sea and air sickness.

    Contraindications:

    Hypersensitivity to the components of the drug. Deficiency of sugar / isomaltase, intolerance to fructose, glucose-galactose malabsorption, age to 18 years.

    Carefully:With caution, appoint patients with diabetes mellitus (the drug contains sugar).
    Pregnancy and lactation:The use of the drug during pregnancy and during breastfeeding is possible.
    Dosing and Administration:

    Validol with glucose is prescribed to adults under the tongue. The tablet should be kept in the mouth under the tongue until it is completely resorbed. Take 1 tablet 2-3 times a day.

    Daily frequency and duration of admission is determined depending on the effectiveness of treatment. If the effect is not sufficiently pronounced, or when the effect is not observed in individual patients within the next 5 minutes after taking the drug, it is necessary to consult a doctor for another therapy.

    Side effects:

    With prolonged reception, slight nausea, lacrimation, dizziness can be observed.These phenomena usually pass by themselves.

    Overdose:

    Symptoms: headache, nausea, agitation, impaired cardiac activity (reflex dilatation of the coronary vessels), a drop in blood pressure, and depression of the central nervous system.

    Treatment: cancel the drug. Symptomatic therapy.

    Interaction:

    When combined with neurotropic drugs, the oppressive type of action enhances the effect of the latter on the central nervous system, promotes the onset of sleep and its deeper course.

    The simultaneous use of Validol with glucose and nitrates reduces the headache that occurs when they are used.

    Special instructions:

    One tablet contains 0.188 g of dextrose (glucose) and 0.511 g of sucrose (sugar), which corresponds to 0.058 XE. This should be taken into account by patients with diabetes mellitus.

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

    During the treatment period, care must be taken when driving vehicles and engaging in other potentially hazardous activities that require increased concentration and speed of psychomotor reactions (with dizziness).

    Form release / dosage:

    Tablets of sublingual 60 mg.

    Packaging:

    For 6 or 10 tablets in a contour mesh box made of polyvinylchloride film and aluminum foil printed lacquered.

    1,2,3, 5 contour mesh packages together with instructions for use are placed in a pack of cardboard.

    It is allowed to use contour packs with an equal number of instructions for use in group packaging.

    Storage conditions:

    In a dry place at a temperature of 12 to 15 ° C.

    Keep out of the reach of children.

    Shelf life:

    2 years.

    After the expiry date, the drug should not be used.

    Terms of leave from pharmacies:Without recipe
    Registration number:P N003674 / 01
    Date of registration:15.07.2011
    Expiration Date:Unlimited
    The owner of the registration certificate:MEDISORB, CJSC MEDISORB, CJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp19.01.2017
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