Active substanceNeomycinNeomycin
Similar drugsTo uncover
Dosage form: & nbspaerosol for external use
Composition:

Composition per 1 g of the preparation:

Active substance: neomycin sulfate (in terms of neomidine) 11.72 mg. Excipients: sorbitan trioleate 10.3 mg, lecithin 0.2 mg, isopropyl myristate 134.0 mg, propellant (propane / butane / isobutane) 843.8 mg.

Description:a white or almost white white suspension with a characteristic odor.
Pharmacotherapeutic group:antibiotic aminoglycoside
ATX: & nbsp

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

D.06.A.X.04   Neomycin

Pharmacodynamics:

Aminoglycoside antibiotic. It disrupts protein synthesis, suppressing the formation of a complex of transport and matrix RNA. In low concentrations bacteriostatic effect (due to violation of protein synthesis in microbial cells), in high concentrations - bactericidal (damages the cytoplasmic membranes of the microbial cell). Penetrates into the microbial cell, binds to specific receptor proteins on 30S subunit of ribosomes. Violates the formation of the complex transport and matrix RNA (30S subunit of the ribosome) and stops protein synthesis. It is active against a number of gram-positive and gram-negative aerobic microorganisms: Staphylococcus spp., Streptococcus spp.; moderately active in relation to aerobic bacteria - Corynebacterium diphtheriae, Listeria monocytogenes; enterobacteria - Escherichia coli, Salmonella spp.,.Shigella spp., Proteus spp., Enterobacter aerogenes, Klebsiella pneumonia, Vibrio cholerae; Mycobacterium tuberculosis, Haemophilus influenzae; He acts on Pseudomonas aeruginosa, anaerobic bacteria.

The resistance of microorganisms to neomycin develops slowly and to a small extent.

A drug Neomycin aerosol for external use inhibits the development of bacterial flora in the foci, inflammation of the skin. It also has drying and cooling effect.

Pharmacokinetics:

Neomycin applied to the intact skin surface acts locally and practically not absorbed into the blood. When applied to damaged skin neomycin can be absorbed into the blood and cause systemic action.

Indications:

Infectious-inflammatory skin diseases caused by sensitive to neomycin by microorganisms (including furunculosis, contagious impetigo);

Infected burns and frostbites of I and II degrees.

Contraindications:

Hypersensitivity to neomycin or other components includedin the composition of the drug;

Violation of the integrity of the skin, extensive "lesion area, wetting in place application, trophic ulcers;

Simultaneous use with other oto-and nephrotoxic drugs;

Childhood.
Carefully:
Pregnancy and lactation:When pregnancy can be prescribed only in cases where the potential benefit to the mother exceeds the possible risk to the fetus. If it is necessary to use the drug during lactation, breastfeeding should be discontinued.
Dosing and Administration:Outwardly. Before each use, shake the bottle several times vigorously. Affected areas are sprayed with aerosol for 3 seconds, keeping the balloon in a vertical position about 15-20 cm from the skin surface. The procedure is carried out 1-3 times a day at the same time intervals. Usually the drug is used 7-10 days.
Side effects:

At external application, in a place of application of a preparation, allergic reactions (an itch, an eruption, a hyperemia, an edema) are possible.

Prolonged use of neomycin may lead to contact allergies.

If any of the side effects listed in the manual are aggravated, or if you notice any other side effects not listed in the instructions, report on this doctor.

Overdose:

Symptoms: itching, rash, hyperemia, edema, nephrotoxicity, ototoxicity.

Treatment: discontinuation of the drug, rapid elimination of the drug from the body, symptomatic therapy.
Interaction:

In order to avoid possible drug interactions with neomycin, other drugs can be used only after consultation with the doctor. �?

Prolonged use of the drug simultaneously with oto- and nephrotoxic drugs (including with gentamycin, ethacrynic acid, colistin) can enhance the toxicity of neomycin.
Special instructions:

Avoid contact with mucous membranes.

It is necessary to protect the eyes from the effects of aerosol. In case of contact with eyes or mucous membranes, rinse thoroughly with cool water.

Do not inhale the sprayed product.

Do not apply the drug to a large surface of the skin, especially damaged, and also under occlusive dressing because of the possibility of absorption of the drug into the blood and the appearance of undesirable reactions characteristic of the systemic action of the drug (ototoxicity, nephrotoxicity). If the above undesirable effects occur, the drug should be immediately discontinued.

In case of irritation of the skin at the site of application, it is necessary to stop using the drug.

Long-term use of the drug may lead to the growth of resistant strains of bacteria and fungi.

The contents of the cylinder are under pressure; Balloon Do not strike, heat, or open; Empty the balloon must be discarded. The drug is highly flammable. Do not spray near open flames. Keep container away from open flames and operating heating devices.

Effect on the ability to drive transp. cf. and fur:The drug does not affect the ability to drive vehicles and engage in other potentially hazardous activities that require increased concentration and speed of psychomotor reactions.
Form release / dosage:

Aerosol for external use, 1,172%

16 g or 32 g of the preparation into an aerosol can with a valve and a spray device. A balloon along with the instruction for use is placed in a cardboard box.

Packaging:aerosol for external use (balloon) 16/32 g х 1
Storage conditions:

Store at a temperature not exceeding 25 ° C.

Keep out of the reach of children.

Shelf life:

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

Terms of leave from pharmacies:On prescription
Registration number:LP-001197
Date of registration:11.11.2011
The owner of the registration certificate:Tarkhominsky pharmaceutical factory "Polfa", A.O.Tarkhominsky pharmaceutical factory "Polfa", A.O. Poland
Manufacturer: & nbsp
Representation: & nbspTARHOMINSK PHARMACEUTICAL FACTORY POLFA JSC TARHOMINSK PHARMACEUTICAL FACTORY POLFA JSC Poland
Information update date: & nbsp06.08.2015
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