Ravisol tincture 100 ml

Author Ольга Кияница

2017-05-11

Amount in a package -
Product form Tincture
Manufacturer Red Star JSC (Ukraine, Kharkov)
Registration certificate UA/9617/01/01
The main medicament Ravisol
morion code 126231

Ravisol instruction manual

Composition:

active ingredient: 100 ml contains: tincture (1:10) from a mixture of medicinal plant raw material "Ravisol": mistletoe of white shoots and leaves (visci albi сormi et folia) - 1,5 g; horsetail of field grass (equiseti arvensis herba) - 1 g; Sophora Japanese fruit (sophora japonica fructus) - 1.5 g; chestnut horse seed (hippocastani semina) - 1.5 g; hawthorn fruits (crataegi fructus) - 2 g; clover flowers (trifolii flores) - 1 g; periwinkle of small grass (vincae minoris hegba) - 1.5 g;(extragent ethanol 40%);
auxiliary substances: none, except extractant.

Dosage form

Tincture.

Pharmacotherapeutic group

Lipid-lowering drugs.

Pharmacological properties

Ravisol reduces the level of total blood lipids, cholesterol, triglycerides, β-lipoproteins, improves cerebral and coronary blood flow, is a sodium diuretic, reduces the activity of the vasculature and peripheral vascular resistance. It has antiplatelet and hypocoagulation effect, increases the efficiency of myocardial contractile activity, stabilizes the lysosomal membranes and reduces the permeability of the plasma-lymphocyte barrier, has anti-inflammatory effect.

Indications for use

Atherosclerosis, vegetative-vascular dystonia (in complex therapy). Headache, dizziness; to improve memory, focus, and to improve the overall condition and performance of older people.

Contraindications

Hypersensitivity to any of the components of the drug. Nephrites, nephroses, nephronesphritis. Severe kidney disease, chronic renal failure. The expressed form of an arterial hypotension, a bradycardia.

Interaction with other drugs and other interactions

The effect of Ravisol is reduced when used with Almagel and Venter, as a result of the binding of flavonoids and tannins of the Ravisol preparation with heavy metals that are part of the above preparations. The effect of the drug reduces sulfur-containing solutions for intravenous administration (sodium thiosulfate). The drug increases the effect of anticoagulants, so if you need a simultaneous appointment with anticoagulants, the dose of the latter should be reduced (under the control of the prothrombin index). The drug should not be used simultaneously with aminoglycoside antibiotics, cephalosporins. Can potentiate the effect of antiarrhythmic drugs. the drug enhances the effects of cardiac glycosides, hypnotics, sedatives, hypotensive drugs. Reception with salts of alkaloids is not recommended in connection with the possibility of formation of negative complexes. Do not use the drug with cisapride.

Application features

The drug should be applied diluted. Before starting the drug, prescribe a standard hypocholesterol diet, which must be followed during treatment. Before starting, and also during the course of treatment with the drug, it is necessary to perform a study of liver function. When using the drug should monitor the function of the kidneys. Use with caution in patients with allergic diseases.

Use during pregnancy or lactation

During pregnancy or breast-feeding the drug is contraindicated. If you need to use the drug, breast-feeding for the period of treatment should be discontinued.

The ability to influence the reaction rate when driving or working with other machinery

In connection with the content of ethanol should be taken with caution when driving vehicles and working with potentially dangerous mechanisms.

Dosing and Administration

Adults and children from 16 years of age, the drug should be administered orally. Take with a small amount of water 1 teaspoonful (5 ml) 3 times a day for half an hour before meals. Before use, the preparation should be shaken. The course of treatment is 10 weeks.

Children

The drug is contraindicated in children under 16 years.

Overdose

Symptoms: possible manifestations of prooxidant properties (acceleration of oxidation-reduction processes, including lipid peroxidation, lipid metabolism acceleration, enzyme conversion), accompanied by disorders of the structure and function of cell membranes and the functions of organs, especially the liver, heart and kidneys. In case of exceeding the recommended doses, there may be: increased side effects, nephrotoxic reactions, arterial hypotension, thrombosis, possibly the occurrence of drowsiness, bradycardia, requiring discontinuation of the drug and symptomatic therapy.

Adverse Reactions

From the digestive tract: pain in the epigastric region, nausea, vomiting, diarrhea.
From the cardiovascular system: accelerated heartbeat, lowering blood pressure.
Allergic reactions, including hives, redness of the skin, a feeling of heat, rash, itching.
On the part of the kidneys and urinary system: can irritate the kidney tissue, manifested by pain in the lower back and at the end of urination.

Shelf life

2 years. Do not use after the expiry date printed on the package.

Storage conditions

Store in the original packaging at a temperature not higher than 25 ° C. Keep out of the reach of children.

Packaging

For 100 ml in a vial polymer or glass; on 100 ml in the bank. One bottle or a jar in a cardboard box.

Category of leave

Without recipe.


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