Active substanceSodium tetraborateSodium tetraborate
Dosage form: & nbspSolution for local and external use.
Composition:

Active substance: sodium tetraborate decahydrate - 20 g; auxiliary substance, glycerol (glycerol) - 80 g.

Description:

Colorless viscous liquid.

Pharmacotherapeutic group:antiseptic
ATX: & nbsp

D.08.A.D   Preparations of boric acid

Pharmacodynamics:

Antiseptic. Has bacteriostatic activity. Effective in candidiasis. Removes the mycelium of the fungus from the mucous membranes, disrupts the process of attachment of the fungus to the mucous membranes and inhibits its multiplication (it is not an antifungal drug, t.does not have a fungicidal or fungistatic effect). As an antimicrobial drug is part of the combination of drugs for the treatment of inflammatory diseases of the upper respiratory tract. Has insecticidal properties (Class IV toxicity).

Pharmacokinetics:

Absorbed in the gastrointestinal tract and through damaged skin. It is deposited in bone tissue and liver. It is excreted by the kidneys in unchanged form and through the intestine for 1 week.

Indications:

Candidiasis lesions of the mucous membrane of the oral cavity, pharynx, upper respiratory tract, urinary tract and genital organs; intertrigo, decubitus.

Contraindications:

Hypersensitivity to the components of the drug, pregnancy, lactation, children up to 3 years. Violation of the integrity of the skin (with the treatment of the skin).

Carefully:
Pregnancy and lactation:The use of the drug is contraindicated in pregnant women, during lactation.
Dosing and Administration:

Locally and externally.

Age category of patients: adults, children from 3 years.

Used for rinsing, lubricating the skin, douching 2-3 times a day. Treatment is carried out as necessary, until the symptoms of the disease are eliminated.Features of the drug during the first admission or when it is canceled are absent.

The features of medical use of the drug for adults with chronic diseases are absent.

Side effects:

Hyperemia and burning sensation in the place of application.

Overdose:

Symptoms of accidental ingestion (a lethal dose for adults - 10-20 g, toxic concentration in the blood - 40 mg / l, fatal - 50 mg / l): abdominal pain, vomiting, decreased appetite, diarrhea, dehydration, weakness, confusion consciousness, dermatitis, menstrual irregularities, anemia, twitching of the muscles of the face and limbs, allopecia, impaired function of the heart, liver and kidneys.

Treatment: gastric lavage, forced diuresis, with severe poisoning - hemodialysis, IM - riboflavin mononucleotide 10 mg / day, correction of water-electrolyte balance and acidosis: intravenous infusion of sodium bicarbonate solution, plasma-substituting solutions, sodium chloride solution and dextrose . For pain in the abdomen, 1 ml of 0.1% solution of atropine, 1 ml of 0.2% solution of platifillin, 1 ml of 1% solution of promedol, iv - dextrose-procaine mixture (50 ml of 2% solution of procaine and 500 ml of 5% solution dextrose).Maintaining the functions of the cardiovascular system.

Information about the symptoms of overdose with local and external use of the drug is absent.

Interaction:There is no information.
Special instructions:

The condition of effectiveness for monotherapy of vaginal candidiasis is the need for medical procedures by medical personnel, multiple treatments; otherwise, fungal cells may linger in the vaginal crypts and lead to a relapse.

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

There is no information.

Form release / dosage:Solution for local and external use.
Packaging:

For 30 and 50 g of the drug in bottles of orange glass with a screw neck, or 50 grams in vials of polymer, bottles of high-density polyethylene or low pressure.

Each bottle, together with the instructions for use, is placed in a pack of cardboard. It is allowed to pack bottles in a group package (carton box) with an equal number of instructions for use.

Storage conditions:

In the dark place at a temperature of no higher than 30 ° C.

Keep out of the reach of children.

Shelf life:

3 years. Do not use after the expiration date indicated on the label.

Terms of leave from pharmacies:Without recipe
Registration number:LP-001806
Date of registration:17.08.2012
The owner of the registration certificate:SAMARAHEDPROM, JSC SAMARAHEDPROM, JSC Russia
Manufacturer: & nbsp
Information update date: & nbsp17.08.2012
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