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

    Composition per one tablet:

    Active substance:

    Levomenthol solution in menthyl isovalerate 0.06 g

    Excipients:

    Sucrose (sugar) 1.158 g

    Calcium stearate monohydrate 0.005 g.

    Description:

    Round tablets of flat-cylindrical shape, with a risk on one side and chamfer, white with a yellowish shade of color with grayish patches, with a characteristic odor.

    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, histamine, kinins (due to irritation of mucosal receptors), which take an active part in the regulation of vascular permeability, the formation of pain. With sublingual admission, the therapeutic effect on average occurs in 5 minutes, while up to 70% of the drug is released within 3 minutes.

    Pharmacokinetics:

    With sublingual administration levomenthol absorbed from the oral mucosa, is 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 drug components, sugarase / isomaltase deficiency, fructose intolerance, glucose-galactose malabsorption,age under 18 years (there is no data on the efficacy and safety of the drug in children).

    Carefully:

    Diabetes mellitus (the drug contains sugar).

    Pregnancy and lactation:

    The purpose of the drug during pregnancy and during breastfeeding is possible, if the expected benefit to the mother exceeds the potential risk to the fetus and the baby.

    Dosing and Administration:

    Validol appoint adults to 1 tablet under the tongue until it is completely absorbed. Take 1 tablet 2-3 times a day. Multiplicity and duration of admission is determined depending on the effectiveness of treatment. If there is no or Inadequate manifestation of the therapeutic effect in the next 5-10 minutes after taking the drug should consult a doctor for the appointment of another therapy.

    Side effects:

    There may be nausea, lacrimation, dizziness. With the withdrawal of the drug, these side effects usually pass by themselves. Perhaps the development of allergic reactions (skin rash, itching, angioedema). If side effects occur that are not described in this manual, you should stop taking the medication and tell your doctor about it.

    Overdose:

    Symptoms: headache, nausea, an excited state, a violation of the heart, a sharp decrease in blood pressure, suppression of the central nervous system.

    Treatment: withdrawal of the drug, symptomatic therapy.

    Interaction:

    When used simultaneously with drugs that depress the central nervous system, enhances the effect of the latter.

    Simultaneous use of the drug with nitrates reduces the headache that occurs when they are used.

    Special instructions:

    It is not recommended to drink alcohol at the same time. Use with caution in patients with diabetes mellitus (the drug contains sucrose). The amount of sucrose in 1 tablet corresponds to 0.09 XE (bread units).

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

    When taking the drug, care must be taken when carrying out potentially dangerous activities requiring increased concentration of attention and speed of psychomotor reactions (vehicle management, work with moving mechanisms, dispatcher, operator).

    Form release / dosage:

    Tablets of sublingual 60 mg.

    Packaging:

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

    For 2, 3, 4, 5 contour mesh packages together with the instruction for use are placed in a pack of cardboard box or cardboard chromium-ersatz For hospitals: 50, 100, 200 contour mesh packages together with an equal number of instructions for use are placed in boxes of corrugated cardboard.

    Storage conditions:

    In a dry, protected from light place at a temperature of no higher than 25 ° C.

    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-004613
    Date of registration:25.12.2017
    Expiration Date:25.12.2022
    The owner of the registration certificate:TULA PHARMACEUTICAL FACTORY, LTD. TULA PHARMACEUTICAL FACTORY, LTD. Russia
    Manufacturer: & nbsp
    Information update date: & nbsp24.01.2018
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