Active substanceKanamycin + Nitrofural + [Calcium chloride + Gelatin]Kanamycin + Nitrofural + [Calcium chloride + Gelatin]
Similar drugsTo uncover
Dosage form: & nbspsponge
Composition:

Kanamycin sulfate 37500 ED, furacilin 0.0015 g, calcium chloride 0.0015 g, sulfanol NP-3 0.006 g, food grade gelatin up to a sponge mass of 1 g.

Description:The dry porous mass of yellowish color, soluble in water, in the form of plates measuring (60 ± 0.5) x (80 ± 0.5) mm and a thickness of at least 0.6 cm, is easily cut.
Pharmacotherapeutic group:Antimicrobial agent
ATX: & nbsp

D.06.A.X   Other antibiotics for external use

Pharmacodynamics:

It has a prolonged antibacterial and hemostatic effect, stimulates reparative processes in the wound and accelerates its healing. Tamponade of the wound with a sponge leads to a rapid and persistent haemostatic effect. Antibacterial action of the drug is expressed in relation to gram-positive and gram-negative microflora.

Pharmacokinetics:

When applied to the wound, the antiseptic sponge with kanamycin swells within 5-10 seconds and absorbs the fluid in amounts exceeding 30-40 times its own weight. At the same time, a depot of the antibiotic kanamycin sulfate is locally created. As the drug dissolves under the action of proteolytic enzymes kanamycin enters the wound in bactericidal concentrations. Within 10-14 days, the sponge left in the wound is completely absorbed.

Indications:

An antiseptic sponge with kanamycin is used in adults.

When providing first aid for wounds and burns of any location as a means of personal protection.

In the treatment of infected wounds of different localization and origin.

For biological coating in the complex treatment of thermal, chemical and radiation burns of varying severity and localization.

In the treatment of trophic ulcers in order to stimulate reparative processes and accelerate the healing of wounds.

As a plastic material for filling infected cavities after sequestrectomy in patients with osteomyelitis.

For the prevention of postoperative complications and the development of wound infection.

As a haemostatic agent for various bleedings, including capillary and parenchymal, arising from surgical interventions and injuries.

In dental practice, for halting bleeding in patients with hemophilia.

Contraindications:

Hypersensitivity to any of the components of the drug.

Pregnancy, lactation, children's age.

Pregnancy and lactation:The use is contraindicated.
Dosing and Administration:

The drug "Antiseptic sponge with kanamycin" is applied topically.

For wounds and burns, the plates are placed on the wound surface until the penetration of the wound separates, followed by the application of an aseptic dressing. The subsequent dressings are carried out taking into account the speed of resorption of the sponge, which depends on the amount and nature of the wound detachable. Treatment is carried out until a healthy granulation and epithelialization of the wound.

In order to prevent postoperative infectious complications, the sponge is injected into the wound after the end of the operation.

To achieve the hemostatic effect, the sponge plate is pressed against the bleeding spot for 1-2 minutes, as the sponge becomes impregnated with blood, new plates are placed until the bleeding stops completely.

The use of a sponge does not require its subsequent removal. The sponge left in the wound dissolves itself.

The quantities of the preparation used for prevention and treatment are determined by the magnitude and extent of the wound surfaces.The total content of kanamycin sulfate for single use should not exceed 1 million units.

Side effects:

Side effects of the drug are not identified.

Interaction:

When using a sponge antiseptic with kanamycin in the complex treatment of surgical diseases incompatibility with other medicinal products is not revealed.

Form release / dosage:

Sponge.

Packaging:Each sponge is packaged in a combined package: one side of waxed paper, the other of a polymer film. The package is placed in a box of cardboard with instructions for use.
For hospitals - 100, 200, 300 packages, sealed in bags of PVC together with instructions for the use of the drug, placed in a box of cardboard.
Storage conditions:

In a dry place, protected from light, out of reach of children, at a temperature not exceeding + 25 ° C.

Shelf life:

2 years. Do not use after the time specified on the package.

Terms of leave from pharmacies:Without recipe
Registration number:P N003443 / 01
Date of registration:25.02.2010
Expiration Date:Unlimited
The owner of the registration certificate:PECHERY FIRM, LLC PECHERY FIRM, LLC Russia
Manufacturer: & nbsp
Information update date: & nbsp11.05.2017
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