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

    For 1 tablet of 60 mg:

    Active substance: levomenthol solution in mentilizovalerate (Validol) - 60.00 mg.

    Excipients: sucrose - 1157.00 mg; magnesium stearate - 6,00 mg.

    Description:Oval, biconvex tablets white or almost white with grayish patches, with a risk on the one hand, 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. Encourages the production and release (due to stimulation of the mucosal receptors) enkephalins, endorphins and a number of other peptides, histamine, kinin, which actively participate in the regulation of vascular permeability and the formation of pain.

    With sublinual (sublingual) admission, the therapeutic effect develops approximately 5 minutes after taking the drug, while up to 70% of the drug is released within 3 minutes.

    Pharmacokinetics:

    With sublingual (under the tongue) application levomenthol absorbed from the oral mucosa. After suction levomenthol 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, sugar / isomalgase deficiency, fructose intolerance, glucose-galactose malabsorption, age under 18 years (no data on the efficacy and safety of the drug in children).

    Carefully:FROMdiabetes mellitus.
    Pregnancy and lactation:

    The use of the drug during pregnancy and during breastfeeding is possible if the intended benefit to the mother exceeds the potential risk to the fetus or child.

    Dosing and Administration:

    The drug is prescribed for adults 1 tablet under the tongue until it is completely resorbed.

    Take 1 tablet 2-3 times a day. Multiplicity and duration of admission is determined depending on the effectiveness of treatment.

    In the absence or inadequacy of the therapeutic effect in the next 5-10 minutes after taking the drug, you need to see a doctor for another therapy.

    Side effects:

    Nausea, lacrimation, dizziness are possible. With the withdrawal of the drug, these side effects usually pass by themselves.

    Perhaps the development of allergic reactions (skin rash, itching, angioedema).

    Overdose:

    Symptoms: nausea, headache, a sharp decrease in blood pressure, suppression of the central nervous system, a violation of cardiac activity, a state of arousal.

    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 reception with nitrates helps to reduce 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). 1 tablet contains 0.096 XE.

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

    10, 20, 30, 40, 50 or 100 tablets in cans of polyethylene terephthalate for medicinal products sealed with caps screwed with a first opening control or a "push-turn" system made of polypropylene or polyethylene, or cans of polypropylene for medicinal products sealed with lids with the control of the first opening from polyethylene, or polypropylene cans for medicines, sealed with caps tightened with the control of the first opening of high pressure polyethylene.

    One jar or 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90 or 100 of the contour mesh packages together with the instruction for use are placed in cardboard packaging (bundle).

    Storage conditions:

    In the dark 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-003931
    Date of registration:01.11.2016
    Expiration Date:01.11.2021
    The owner of the registration certificate:ATOLL, LLC ATOLL, LLC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp19.01.2017
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