Active substanceBetagistinBetagistin
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  • Dosage form: & nbsppills
    Composition:

    Each tablet contains:

    of the active substance: betahistine dihydrochloride 24 mg.

    Excipients: Povidone K-90 6,0 mg, microcrystalline cellulose 99,0 mg, lactose monohydrate 210.0 mg, silicon colloidal dioxide 7.5 mg, crospovidone 18.0 mg, stearic acid 13.5 mg.

    Description:

    Round, biconvex tablets from white to almost white, with a risk on one side.

    Pharmacotherapeutic group:Histamine drug
    ATX: & nbsp

    N.07.C.A.01   Betagistin

    Pharmacodynamics:

    Synthetic analog of histamine, has a histamine-like and vasodilating effect. Is a weak agonist H1receptors and a rather potent H antagonist3receptors. Affects the cochlear blood flow and central vestibular apparatus.

    The action of betagistin includes: vasodilation in the inner ear (indirectly through H3 and H1receptors), the inhibitory effect on vestibular nuclei (via H3receptors) and impulsive activity of ampullar receptors. By direct agonistic action on H1receptors of the vessels of the inner ear and precapilar sphincters of the microcirculatory bed located in the vascular stripe (stria vascularis), and also indirectly through H3-receptors improves microcirculation and permeability of capillaries, normalizes the pressure of the endolymph in the labyrinth and cochlea, increases blood flow in the basilar artery.

    Has a pronounced central effect, being an antagonist of H3receptors of the nuclei of the vestibular nerve, normalizes neuronal transmission in the polysynaptic neurons of the vestibular nuclei at the level of the brainstem. Influencing H indirectly3receptors, increases the content of serotonin in the brain stem, which reduces the activity of the vestibular nuclei.

    Helps eliminate violations from both the vestibular and cochlear apparatus: reduces the frequency and intensity of dizziness, reduces tinnitus, helps improve hearing in cases of its decline.

    Stimulates H1receptors, so it does not have a sedative effect and does not cause drowsiness.

    Pharmacokinetics:

    Absorbed quickly, the connection with plasma proteins is low. FROMmOh (the maximum concentration in blood plasma) is 3 hours. It is almost completely excreted by the kidneys in the form of a metabolite (2-pyridylacetic acid) for 24 hours. T1/2 (half-life) - 3-4 hours.

    Indications:

    A drop in the labyrinth of the inner ear, vestibular and labyrinthine disorders: dizziness, noise and pain in the ears, headache, nausea, vomiting, hearing loss; vestibular neuritis, labyrinthitis, benign positional dizziness (including after neurosurgical operations), Meniere's disease.

    As part of complex therapy - vertebrobasilar insufficiency, posttraumatic encephalopathy, atherosclerosis of cerebral vessels.

    Contraindications:

    Hypersensitivity, pheochromocytoma, bronchial asthma, peptic ulcer of the stomach and duodenum in the phase of exacerbation, pregnancy (I trimester).

    Carefully:

    Stomach ulcer or 12 duodenal ulcer (in the anamnesis), pregnancy (II-III trimester), children's age.

    Dosing and Administration:

    Inside, with food, without chewing, squeezed a small amount of liquid, to 1/2 -1 tablet 2 times a day. The maximum daily dose is 48 mg.

    Side effects:

    Dyspepsia (nausea, vomiting), skin rash, swelling of Quincke.

    Overdose:

    Symptoms: headache, hyperemia of the facial skin, dizziness, tachycardia, lowering blood pressure (BP), bronchospasm.

    Interaction:

    Antihistamines reduce the effect of taking the drug.

    Special instructions:

    Therapeutic effect in a number of cases appears only a few months after the start of treatment.

    Form release / dosage:Tablets 24 mg.
    Packaging:

    For 10 or 14 tablets in a blister of PVC / PVDC / aluminum foil or PVC / aluminum foil / OBA / aluminum foil.

    For 3, 6 or 10 blisters for 10 tablets or 2 blisters for 14 tablets together with instructions for use in a cardboard box.

    Storage conditions:

    In a dry, dark place, at a temperature of no higher than 25 FROM.

    Keep out of the reach of children

    Shelf life:

    3 years.

    Do not use after the expiration date printed on the package.

    Terms of leave from pharmacies:On prescription
    Registration number:LSR-004481/07
    Date of registration:06.12.2007 / 03.12.2013
    Expiration Date:Unlimited
    The owner of the registration certificate:AKTAVIS GROUP, AO AKTAVIS GROUP, AO Iceland
    Manufacturer: & nbsp
    Representation: & nbspAktavis, Open Company Aktavis, Open Company
    Information update date: & nbsp07.02.2017
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