Tricresol, Phenol

Instruction manual

For medical use of the drug

Ferezol

(pheresol)

Structure:

Active ingredients: 1 g of liquid contains phenol 600 mg, tricresol 400 mg.

Dosage form.

The skin fluid.

Basic physical and chemical properties: lightly moving oily liquid from light brown to dark brown in color with the smell of phenol.

Pharmacotherapeutic group.

Means used in dermatology. agents used to remove warts and calluses.

ATX code D11A F.

Pharmacological properties.

Pharmacodynamics

Feresol is a combined drug that has a cauterizing and bactericidal effect. The mechanism of antimicrobial action is the irreversible coagulation of proteins that make up the vital structures of the pathogen (cytoplasmic membrane, flagella), which leads to the loss of the functions that they perform and the death of the microbe. The drug does not have a pronounced selectivity for certain types of microbes, active in relation to gram-positive, gram-negative bacteria, fungi, viruses, protozoa. The cauterizing mechanism is due to the destruction of the macromolecules of cells and fibers of the skin and mucous membranes (chemical burn). Contact with body tissues causes chemical burns.

Pharmacokinetics

Not installed.

Clinical characteristics.

Indications.

For removal of papillomas, genital warts of the skin, keratomas, warts, dry corns.

Contraindications

Hypersensitivity to the drug. nevi.

Interaction with other drugs and other types of interactions.

The components of the drug are easily dissolved in an ointment base, and therefore it is not recommended to lubricate any area of ​​the skin treated with phenol with any ointments.

Features of the application.

Inadmissibility of the drug in the eyes and mucous membranes. bandaging of the skin area treated with the preparation, removal of scabs is not allowed; You can not reapply the drug before the above dates. synthetic skin should not come in contact with skin areas treated with feresol.

To prevent dermatitis, the area treated with Feresol should dry in the open air. The area on which Ferezol was applied cannot be lubricated with any ointments; washing with water is allowed. When used correctly, the drug does not leave scars.

Do not treat Feresol with a skin surface of more than 20 cm².

Use during pregnancy or lactation.

The use of the drug during pregnancy or lactation is possible only when the expected benefit to the mother outweighs the potential risk to the fetus or child.

During breastfeeding, it is not recommended to remove formations located on the mammary glands and hands.

The ability to influence the reaction rate when driving vehicles or other mechanisms.

Does not affect. when feresol is treated with a skin area near the eye, retinal edema may occur, which can adversely affect visual acuity. in this case, you must avoid driving or working with other mechanisms.

Dosage and administration.

Feresol is used by adults only in a hospital setting and only externally. the drug is applied directly to the treated formations, avoiding its contact with neighboring areas of the skin and especially the mucous membrane. papillomas, warts, condylomas are lubricated continuously for 10-60 minutes (depending on their size). in the presence of papillomas having a thin leg, only the leg is lubricated. re-treatment is carried out 6-8 days after the scab falls off.

Warts on the hands, keratomas, dry corns with keratinization symptoms are pre-softened by steaming, and then lubricated with the drug continuously for 1 hour.If necessary, after 2 weeks, this procedure can be repeated. 4-5 procedures are allowed.

Each procedure is carried out by wetting Feresol with solid turunda from surgical cotton, carefully applying the drug to the treated surface.

Children.

Do not use in children.

Overdose.

If the drug enters a large area of ​​the skin surface, a chemical burn is possible, general intoxication of the body.

Treatment. Therapy is symptomatic.

Adverse Reactions

On the part of the skin: treatment with a feresol skin area near the eye can cause retinal edema, which usually passes on its own.

From the immune system: in some cases, allergic reactions are possible.

General reactions and reactions at the application site: burning sensation at the application site.

Shelf life.

4 years.

Storage conditions.

Store in the original packaging at a temperature not exceeding 25 ° C.

Keep out of the reach of children.

In case of precipitation of crystals, the vial must be heated before use in a water bath at a temperature of 30 ° C to 40 ° C, slightly shaking its contents; after dissolving the crystals, the drug is suitable for use. Do not use the drug after the expiration date.

Packaging.

15 g in bottles No. 1.

Vacation category.

On prescription.

Manufacturer.

Pao Lubnypharm.

The location of the manufacturer and his address of the place of business.

Ukraine, 37500, Poltava region, Lubny, st. Barvinkova, 16.