Iod-Ka - instructions for use, dose, side effects, contraindications

Excipients: glycerol (in terms of anhydrous substance) 1.05 g, citric acid (based on dry matter) 0.071 g, sodium hydrogen phosphate (based on dry matter) 0.15 g, sodium hydroxide solution 10% to pH 3.0 -6.0, water purified to 100.0 ml.

Description:

The solution is dark brown with iodine.

Pharmacotherapeutic group:antiseptic

ATX: & nbsp

D.08.A.G.02 Povidone-iodine

Pharmacodynamics:

Antiseptic and disinfectant. When released from a complex of iodine with polyvinylpyrrolidone in contact with the skin, iodine forms with iodine proteins, coagulates them, which causes the death of microorganisms. Has a rapid bactericidal effect on Gram-positive and Gram-negative bacteria (with the exception of Mycobacterium tuberculosis). Effective against fungi, viruses, protozoa. It has a longer action than the inorganic iodine solution.

Pharmacokinetics:

When topical application is almost no absorption of iodine from the surface of the skin and the mucous membrane of the wound.

Indications:

- Treatment of bacterial, fungal and viral skin infections;

- treatment and prevention of wound infections in surgery, traumatology, kbustustologii;

- treatment of pressure sores, trophic ulcers, diabetic foot;

- disinfection of patients' skin in preparation for surgical interventions, invasive examinations (punctures, biopsies, injections, etc.);

- disinfection of the skin around drains, catheters, probes.

Contraindications:

Hypersensitivity to the components of the drug, pregnancy, breastfeeding, neonatal period (especially in premature infants), hyperthyroidism or other severe thyroid dysfunction, thyroid adenoma, thyrotoxicosis, herpetiform dermatitis Duhringa, condition before and after administration of radioactive iodine for the treatment of hyperthyroidism until complete recovery).

If you have one of the listed diseases, before taking the drug necessarily consult a doctor.

Pregnancy and lactation:

There is insufficient data on the use of iodine in pregnant women. Therefore, the use of the drug during pregnancy is not allowed.

Dosing and Administration:

Outwardly.

Apply directly to the damaged surface, capturing the surrounding healthy tissue.

Side effects:

If you get into the mucous membrane of the eye, allergic reactions, burning and lacrimation are possible. In predisposed individuals, iodine hyperthyroidism is rare in rare cases.

Intensive treatment of burn wounds with povidone-iodine can cause violations of electrolyte balance or osmolality of blood serum with impaired renal function or metabolic acidosis.

If any of the side effects indicated in the manual are aggravated, or any other side effects not indicated in the instructions are noted, you should inform the doctor immediately.

Overdose:

Cases of overdose have not been observed to date.

Treatment: symptomatic.

Interaction:

The combined use of the drug with hydrogen peroxide, enzyme preparations containing silver and taurolidine for wound treatment, as well as antiseptic drugs, leads to a mutual decrease in efficiency.

Povidone-iodine can not be used in conjunction with mercury preparations, because this leads to the formation of an alkaline iodide of mercury.

The drug can react with proteins and unsaturated organic complexes.

Avoid prolonged use of the drug, especially on large surfaces, in patients receiving lithium preparations.

Povidone-iodine is incompatible with reducing substances, alkaloid salts, tannic acid, salicylic acid, silver, mercury and bismuth salts.

Special instructions:

Avoid contact with eyes.

The use of povidone iodine may reduce the absorption of iodine by the thyroid gland,which could affect the results of some research and procedures (thyroid scintigraphy, determination of protein-bound iodine, diagnostic procedures using radioactive iodine), and therefore the planning of treatment of diseases of the thyroid gland iodine preparations may be impossible. After discontinuation of the drug should wait an interval of not less than 1-4 weeks.

The oxidative effect of povidone iodine can lead to false positive results from various diagnostic tests (for example, measurements of hemoglobin and glucose in feces and urine using toluidine and guaiac resins).

Oxidizing properties of povidone-iodine can cause corrosion of metals, whereas plastics and synthetic materials are usually not sensitive to povidone-iodine. In some cases, there may be a discoloration, which is usually restored.

The preparation is easily removed from textile and other materials with warm water and soap.

Difficult to remove stains should be treated with a solution of ammonia or sodium thiosulfate.

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

Does not affect.

Form release / dosage:

Solution for local and external use, 10%.

Packaging:

For 10 ml in a glass bottle made of brown glass with a lid with a spatula screwed plastic. Each vial with instructions for Medical application is placed in a pack of cardboard for consumer packaging.

To 25 ml in a glass bottle made of brown glass with a spray. Each vial, along with instructions for medical use, is placed in a pack of cardboard for consumer packagings.

To 50 ml in a glass bottle made of brown glass with a lid with a pipette screwed plastic. Each bottle, along with instructions for medical use, is placed in a pack of cardboard for consumer containers.

On the vials stick a label of paper label or writing or self-adhesive label.

Storage conditions:

In the dark place at a temperature of 5 to 20 ° C.

Keep out of the reach of children.

Shelf life:

3 years

Do not use after expiry date.

Terms of leave from pharmacies:Without recipe

Registration number:LP-001349

Date of registration:13.12.2011

The owner of the registration certificate:GENS, LLC GENS, LLC Russia

Manufacturer: & nbsp

SNEZHFARM, OJSC Russia

Information update date: & nbsp18.08.2015

Illustrated instructions

Instructions

Iod-Ka® (Iod-Ka®)