Solcoderm solution for external use ampoules 0,2ml №1

Dosage form

Solution for external use

Composition

1 ml of the solution for external use contains: Azoya Acid 70% 5807 mg, acetic acid 99% 411 mg, oxalic acid dihydrate 574 mg, lactic acid 90% 45 mg, copper nitrate (II) trihydrate 48 μg.

Excipients: distilled water.

Packing

In the vial of colorless glass 0.2 ml solution. In packaging 1 ampoule complete with a plastic applicator and 2 glass capillaries.

Mechanism of action

Solcoderm - a drug for the local treatment of benign superficial skin lesions.

The complex effect on the affected skin area of ​​the components of Solcoderm provides direct intravital fixation followed by mummification of the diseased tissue with which the drug comes in contact.

The direct effect of the drug is expressed in discoloration of the skin with the appearance of a characteristic pale gray or yellowish tint. Devitalized after exposure to the drug, the fabric becomes dehydrated and, as mummification takes place, becomes dark brown in color. The resulting mummified scab spontaneously exfoliates after a few days or weeks.

Healing happens quickly; Complications such as secondary infection or the occurrence of scar tissue are rarely observed.

Indications and usage

For external use in the treatment of benign skin changes:
- Common warts (Verruca vulgaris).
- Plantar warts (Verruca plantaris).
- Genital warts (Condylomata acuminata).
- Non-cellular nevus, tested for good quality (Naevus naevo-cellularis).

Contraindications

- Malignant neoplasms of the skin, prone to metastasis (including malignant melanoma).
- Pronounced tendency to form scar tissue.

Solcoderm can not be used to remove freckles and keloid scars.

Pregnancy and Breastfeeding

Studies on the possible effects of the drug on the body of women during pregnancy and lactation have not been conducted to date.Use Solcoderm during pregnancy and lactation is possible only in cases where the potential benefits of its use outweighs the possible risk to the fetus or child.

Experimental studies on animals have shown the absence of a risk factor for the fetus.

Dosage and administration

Solcoderm is for external use only; The procedure must be carried out by a doctor or qualified medical personnel under the supervision of a physician.

Before the procedure, the area of ​​the affected skin area is treated with ethyl alcohol or ether. Solcoderm applied directly to the affected skin. For the application of the drug on the skin using a special plastic applicator with sharp and blunt ends, available in the package. The sharp edge is mainly used to apply the drug to small areas of the affected skin; blunt end is used to handle extensive lesions.

As an alternative method of applying the drug is used enclosed glass capillary. Combined skin lesions of 2-3 cm 2 can also be treated with a glass capillary. To fill the glass capillary with the preparation, it is necessary to immerse it in a solution of Solcoderm for several minutes. Special care should be taken when applying, avoiding the application of too large volumes of Solcoderm solution and damage to the deep tissue layers. It is necessary to apply as much of the solution as it absorbs the tissue of the affected skin.

Solcoderm gently applied to the affected skin with a plastic applicator or glass capillary and then spread over the surface of the selected skin with light pressure using a plastic applicator until the solution completely penetrates the fabric. Over the next 3-5 minutes, it is necessary to carefully observe the changes occurring in the treated area: skin discoloration occurs with the appearance of a characteristic pale grayish or yellowish tint. The procedure should be repeated until the above mentioned discoloration of the skin occurs.

When treating keratinized warts, the top layer of the stratum corneum should be removed first.

The affected skin areas with a diameter of more than 10 mm are treated with Solcoderm only if it is determined that only the top layer of the skin is pathologically modified.

In the presence of numerous lesions on the skin, treatment with Solcoderm should be carried out in several stages, with an interval of approximately 4 weeks. During each procedure no more than 2-3 lesions can be treated with a total area of ​​no more than 2-3 cm 2.

Within a few days after the procedure, the treated area of ​​skin acquires a dark brown shade and dries to form a scab. In the case of unsatisfactory mummification of the diseased tissue, it is possible to repeat the procedure after a few days.

In order to facilitate the fixation and mummification of pathologically modified tissues that have undergone treatment, the affected areas should be treated 2-3 times a day with a tampon moistened with 70% ethanol (especially after bathing or washing).

Do not remove the scab by scraping or using mechanical means. The eschar must fall off spontaneously, otherwise a violation of tissue healing processes and the formation of scars may occur.

Adverse reactions

Local reactions: moderate transient erythema and temporary appearance of a white ischemic ring on healthy skin around the site of application of the drug (do not require special treatment); short burning within a few minutes after application of the drug; in very rare cases - a change in skin pigmentation and the formation of scar tissue.

Do not use the drug Solcoderm on inflamed areas of the skin. Special care is required when the drug Solcoderm is treating benign skin tumors that have been previously treated with other drugs, other methods.

After biopsy of the affected skin area, it is recommended to wait 8-10 days before starting treatment with Solcoderm solution. In the treatment of affected skin areas located near the mucous membranes, incl. near the eyes, special precautions should be taken. If Solcoderm solution is accidentally applied to healthy skin, it should be immediately removed with a cotton swab moistened with water.If an accidental contact of Solcoderm solution into the eye has occurred, it is necessary to immediately wash the eye with a large amount of water or with a weak alkaline solution (1% sodium bicarbonate solution). Drops of Solcoderm solution that have fallen on furniture or clothing must be washed off with water, since Solcoderm is capable of destroying the materials from which they are made.

In the event of pain at the time of application of the drug treatment should be promptly interrupted. With the appearance of pronounced local irritation and severe itching on the skin areas adjacent to the site of application of the drug, it is recommended to use a cream containing GCS, or an ointment that has an anesthetic effect.

Until complete healing of the lesion site treated with Solcoderm (approximately 2-4 months after treatment), exposure to direct sunlight and ultraviolet radiation should be avoided. For each therapeutic procedure, you must use a new ampoule, because after opening the ampoule, Solcoderm solution is chemically unstable. The opened ampoule should be stored strictly vertically by fixing it in a special slot of the contour packaging for ampoules.

Before discarding the used ampoule, wash off the rest of the solution in running water. Empty vial can be thrown into the trash.

There are no restrictions regarding the use of the drug Solcoderm in children over 5 years old.

Overdosage

Symptoms: use of the drug Solcoderm in too large doses can cause acid burns and damage to the deeper layers of the skin.
Treatment: an ulcer resulting from an overdose is treated like a normal wound.

Storage conditions

The drug should be stored at a temperature of 8 ° to 20 ° C.