For the local treatment of all forms and stages of psoriasis, allergic, atopic (especially in the subacute period and during the extinction of the process), perioral and seborrheic dermatitis, neurodermatitis, photodermatosis, toxidermia, as well as blistering lichen (herpes) of various localization (labial, buccal, nasal, ear, genital) and shingles.
active substance: fladexan;
1 g of ointment contains fladexan in terms of the content of the sum of flavonoids 30% 20 mg;
excipients: white soft paraffin, propylene glycol, stearic acid, emulsifier No. 1, methylparaben (E 218), propylparaben (E 216), purified water.
Fladex Dosage form
Basic physical and chemical properties: ointment from light brown to dark brown, with a specific odor.
Fladex Pharmacotherapeutic group
Dermatological agents. ATX code D11A X.
A herbal medicine containing fladexan – an extract of the desmodium herb from the Canadian legume family.
The drug has a local anti-inflammatory, analgesic and antiallergic effect, has antiallergic and desensitizing properties, exhibits antiviral activity against the viruses herpes zoster (herpes simplex) and herpes zoster – Herpes simplex and Herpes zoster, and also stimulates reparative processes in the skin.
When applied to the skin, the components of the ointment do not appear in the blood serum.
For local treatment of all forms and stages of psoriasis, allergic, atopic (especially in the subacute period and in the period of extinction of the process), perioral and seborrheic dermatitis, neurodermatitis, photodermatosis, toxidermia, as well as lichen vesicular (herpes) of various localization (labial, buccal, nasal , ear, genital) and shingles.
Hypersensitivity to the components of the drug.
Interaction with other medicinal products and other types of interactions
No data available.
Due to the presence of methylparaben (E 218) and propylparaben (E 216) in the composition, the drug can cause allergic reactions (possibly delayed).
Propylene glycol can irritate the skin.
The ability to influence the reaction rate when driving or operating machinery
Treatment with the drug does not affect the reaction rate when driving or using other mechanisms.
Application during pregnancy or lactation
The drug can be used during pregnancy and lactation.
Method of administration and dosage
Apply to adults and children externally, locally.
Dermatitis of various origins, blistering (herpes) and shingles. The ointment is applied in a thin layer, lightly rubbing, on the affected area of the skin 2-4 times a day, preferably from the moment the first signs of the disease appear. The duration of the course of treatment is 5-14 days.
Psoriasis. Apply the ointment to the affected skin area under wax paper 1-2 times a day. The course of treatment is 10-30 days or more, especially in the case of large plaque forms.
Depending on the results of therapy and in cases of relapse, the course of treatment can be repeated 2-3 times or more.
The drug can be used in children.
Overdose cases are not described.
In some cases, a burning sensation may appear, which disappears after the temporary discontinuation of the drug.