Fukortsin solution for skin application, 25 ml bottle




Instructions for Fukortsin solution for skin application, 25 ml bottle
Composition
active ingredients: 1 ml of solution contains: basic fuchsin – 4 mg, boric acid – 8 mg, phenol – 39 mg, acetone – 0.049 ml, resorcinol – 78 mg, ethanol 96% – 0.095 ml;
excipient: purified water.
Dosage form
The solution is topical.
Main physicochemical properties: dark red liquid with a characteristic odor of phenol.
Pharmacotherapeutic group
Antiseptics and disinfectants. ATX code D08A X.
Pharmacological properties
Pharmacodynamics.
The active ingredients of the drug provide a wide range of antimicrobial effects in cases of skin and mucous membrane lesions caused by infectious agents. The drug also exhibits a fungicidal effect in cases of fungal lesions of the external integuments.
Pharmacokinetics.
Not studied.
Indication
Treatment of skin diseases caused by pathogens sensitive to the components of the drug: various types of dermatophytes (trichophyton, microsporum, epidermophyton), microbial eczema, oily and mixed forms of seborrhea.
Contraindication
Increased individual skin sensitivity to the components of the drug. Children under 12 years of age. Pregnancy, breastfeeding. Chronic allergic dermatoses.
Special safety precautions
Treatment with the drug should be carried out under the supervision of a doctor and the recommended doses should be followed.
Do not apply the drug to large areas of the body and avoid contact with the eyes.
Treatment with the drug should be carried out with caution in patients with impaired renal function.
Interaction with other medicinal products and other types of interactions
The simultaneous use of topical antifungal antibiotics such as griseofulvin, clotrimazole, preparations containing phenol, boric acid, as well as hormonal preparations should be avoided. Allergic reactions may occur when used simultaneously with preparations for external use.
If you are taking any other medications at the same time, you should inform your doctor.
Use during pregnancy or breastfeeding
Do not use in women during pregnancy or breastfeeding.
Ability to influence reaction speed when driving vehicles or other mechanisms
No effect on the ability to drive vehicles or use other mechanisms was detected.
Method of administration and doses
The solution should be applied to the affected areas of the skin and mucous membranes 1-3 times a day until clinical recovery. The course of treatment is determined by the doctor.
Children
Do not use in children under 12 years of age.
Overdose
With prolonged use of the drug and its use on large areas of the skin, phenomena characteristic of phenol poisoning may occur (dizziness, weakness, respiratory disorders, collapse). In the event of such phenomena, it is necessary to provide the patient with access to fresh air, wash the drug off the skin with water and carry out symptomatic treatment.
Overdose may increase side effects and allergic reactions.
Therapy is symptomatic.
Side effects
On the part of the immune system: hypersensitivity reactions, including anaphylactic shock, urticaria, angioedema; local allergic reactions (including rash, hyperemia, edema, itching at the site of application).
Some patients, especially with prolonged use, may experience the following:
From the nervous system: dizziness, weakness, convulsions, confusion, headache.
Respiratory system: respiratory disorders.
Gastrointestinal: nausea, vomiting, diarrhea.
Renal and genitourinary disorders: oliguria.
Skin and subcutaneous tissue disorders: epithelial desquamation.
If such symptoms appear, it is necessary to wash off the drug residues from the skin surface with water; discontinue the drug and prescribe symptomatic therapy.
If any adverse reactions occur, you should consult a doctor!
Expiration date
2 years.
The drug cannot be used after the expiration date indicated on the package!
Storage conditions
Store in the original packaging at a temperature not exceeding 25 °C.
Keep out of reach of children.
Packaging
Bottles of 25 ml each.
Vacation category
Without a prescription.
Producer
PJSC "FITOPHARM".
Location of the manufacturer and its business address.
Ukraine, 84500, Donetsk region, Bakhmut city, Sibirtseva st., 2.
Applicant
PJSC "FITOPHARM".
Location of the applicant.
Ukraine, 02092, Kyiv city, Almaty street, building 12.
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