Indications
- treatment and prevention of vestibular vertigo of various origins;
- syndromes including dizziness and headache, tinnitus, progressive hearing loss, nausea and vomiting;
- Meniere’s disease or syndrome.
$2.00
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Out of stock
Inside, while eating.1/2-1 tablet 3 times a day.
Improvement is usually noted at the beginning of therapy.
A stable therapeutic effect occurs after two weeks of treatment and may increase over several months of treatment.
Long-term treatment. The duration of taking the drug is selected individually.
With caution:
1 tablet contains:
Active substance:
betahistine dihydrochloride 24 mg;
Excipients:
MCC;
lactose (milk sugar);
citric acid monohydrate;
colloidal silicon dioxide (aerosil);
crospovidone;
talc;
magnesium stearate.
1 tablet contains:
Active ingredient:
betahistine dihydrochloride 24 mg;
Auxiliary substances:
MCC;
lactose (milk sugar);
citric acid monohydrate;
colloidal silicon dioxide (aerosil);
crospovidone;
talc;
magnesium stearate.
Betahistine is a histaminergic substance that improves microcirculation.
Pharmacodynamics
Agonist of H1-receptors of the inner ear vessels and antagonist of H3-receptors of the vestibular central nervous system. By direct agonistic action on the H1 receptors of the inner ear vessels, as well as indirectly through exposure to H3 receptors, it improves microcirculation and capillary permeability, normalizes endolymph pressure in the labyrinth and cochlea, and increases blood flow in the basilar artery.
It has a pronounced central effect, being an inhibitor of H3 – receptors of the vestibular nerve nuclei. Improves conduction in neurons of the vestibular nuclei at the level of the brain stem.
The clinical manifestation of these properties is a decrease in the frequency and intensity of dizziness, a decrease in tinnitus, and an improvement in hearing in the case of its decrease.
Pharmacokinetics
Absorbed quickly, binding to plasma proteins is low. The time required to reach MAX is 3 hours —
It is almost completely excreted by the kidneys as a metabolite (2-pyridylacetic acid) within 24 hours. T1/2 — 3-4 hours.
There are insufficient data to assess the effects of the drug during pregnancy and lactation.
In this regard, it is not recommended to take it during pregnancy. Breast-feeding should be discontinued for the duration of treatment.
With caution:
Gastrointestinal disorders, allergic reactions from the skin (skin rash, itching, urticaria), angioedema.
Interactions or incompatibilities with other medicinal products are unknown.
Inside, while eating. 1/2-1 tablet 3 times a day.
Improvement is usually noted at the beginning of therapy.
A stable therapeutic effect occurs after two weeks of treatment and may increase over several months of treatment.
Long-term treatment. The duration of taking the drug is selected individually.
Symptoms: nausea, vomiting, convulsions.
Treatment: gastric lavage, taking activated charcoal, symptomatic therapy.
Patients with a history of gastric or duodenal ulcer, pheochromocytoma, or bronchial asthma should be prescribed the drug under regular medical supervision.
Influence on the ability to drive motor vehicles and manage mechanisms
Betahistine has no sedative effect and does not affect the ability to drive a car or engage in activities that require rapid psychomotor reactions.
Store in a dry place, protected from light, at a temperature not exceeding 25 °C
2 years
Betahistine
By prescription
Tablets
For adults as prescribed by a doctor, For adults
Meniere’s disease, Cerebrovascular Accident
Out of stock
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