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-27% BIFON Gel, 35 g

BIFON Gel, 35 g

BIFON Gel

Manufacturers: DERMAPHARM AG

PZN: 08931229

Dosage: Gel

Content: 35 g

Reward Points: 58

Availability: In stock

$9.45

$6.92

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-27% BIFON Gel, 35 g
  • BIFON Gel, 35 g
  • BIFON Gel, 35 g

Instructions for use for BIFON Gel, 35 g

Bifon gel
Active ingredients: bifonazole, 10 mg/g
Application areas:
Mycoses of the skin, caused by dermatophytes, yeasts, molds and other mushrooms such as Malassezia Furgen and infections by Corynebacterium Minutissimum: Tinea Manuum, Tinea Pedum, Tinea Corporis, Tinea Inguinalis, Pityriasis Versicolor, Superficial Candidoses, Erythrasm.

Detailed instructions for BIFON Gel, 35 g

Field of use

  • The preparation is a broad spectrum antimycotic for the treatment of fungal diseases (mycoses) of the skin.
  • Bifonazole, the active ingredient in this medicine, penetrates into the affected layers of the skin and kills the fungus there. In addition, it has anti -inflammatory (anti -inflammatory).
  • The gel is applied in the case of mushroom diseases (mycoses) of the skin, which are used by dermatophytes, yeasts, mold and other pathogens such as: B. Malassezia Furgen or Corynebacterium Minutissi, such as. B.:
    • Mycoses of the skin and skin folds (tinea corporis and tinea inguinalis)
    • Mycoses between fingers and toes (Tinea Pedis, Tinea Manuum)
    • Kleis mushroom lichen (Pityriasis Versicolor)
    • superficial yeast mushroom diseases (candidoses) of the skin
    • Dwarf lichen (erythrasma).

Active ingredients / ingredients / ingredients

10 mg bifonazole
alpha-cetylstearyl-omega-hydroxypoly (oxyethylene) -30 auxiliary material (+)
Ethanol 96% (v/v) Hedge substance (+)
Isopropyl isostataratatelic (+)
Macrogol 7 glycerolcocococoat auxiliary material (+)
Lactic acid auxiliary material (+)
Water, cleaned auxiliary material (+)
Benzyl alcohol aid (+)

Contradictions

  • The medicine must not be used
    • if you are allergic to Bifonazole or one of the other components of this drug.

dosage

  • Always apply this medicine as described or exactly after the agreement made with your doctor or pharmacist. Ask your doctor or pharmacist if you are not sure.
  • The recommended dose is:
    • Unless otherwise prescribed, the gel is applied 1 times a day, preferably in the evening before going to bed, the affected skin areas are applied thinly and rubbed.
    • A small amount of gel (approx. 1 cm strand length) is usually sufficient for applying and rubbing in for an approximately palm size.

 

  • Duration of the application
    • In order to achieve permanent healing, the treatment with the gel should not be canceled after the acute inflammatory symptoms or subjective symptoms, but - depending on the type of illness - should be carried out over the following treatment times:
    • The duration of treatment is generally
      • Foot mycoses (Tinea Pedum, Tinea Pedis Interdigitalis)
        • 3 Weeks
      • Mycoses on the rest of the body, on hands and in skin folds (Tinea Corporis, Tinea Manuum, Tinea Inguinalis)
        • 2 - 3 Weeks
      • Pityriasis Versicolor, Erythrasma
        • 2 Weeks
      • superficial candidoses of the skin
        • 2 - 4 Weeks
    • The treatment should basically be carried out until the positive mushroom cultures disappeared, but at least 14 days after the complaints subsided.
    • If your clinical picture worsens or after about 1 week there is no improvement, you have to see a doctor.
    • Please speak to your doctor or pharmacist if you have the impression that the effect of the gel is too strong or too weak.

 

  • If you have used a larger amount than you should
    • You can continue treatment with the dose prescribed. No impairments can be expected in the event of a short -term overdose.

 

  • If you have forgotten the application
    • Continue the treatment as stated in the dosage instructions (Wear z. B. the gel not more or more or in larger quantities).

 

  • If you cancel the application
    • Note Splease ask that a sufficiently long application duration of the gel is important in order to achieve complete healing and avoid relapses.
    • So speak to your doctor or pharmacist before you - e.g. B. due to occurring side effects - interrupt the treatment or end it prematurely!

 

  • If you have any further questions about the application of this medicine, please contact your doctor or pharmacist.

Taking

  • A small amount of gel (approx. 1 cm strand length) is usually sufficient for applying and rubbing in for an approximately palm size.
  • Wash the diseased skin areas before each application so that loose skin scales and any residues of the last treatment are removed. Dry them thoroughly after washing, especially poorly accessible areas. B. between the toes.
  • The medicine is best applied to the diseased skin areas thinly in the evening before going to bed and slightly rubbed.

Patient information

  • Warnings and Precautions
    • Please speak to your doctor or pharmacist before using the preparation.
    • If in the past you have reacted to other medicines against fungal infections (e.g. with the active ingredients Econazole, Clotrimazole, Miconazole), you may only use the medicine with caution.
    • Avoid putting the gel in the eye.
    • If the symptoms continue after treatment, please see a doctor.
    • AntiMycotic treatment of the skin of the nail bed with the gel can only be carried out after preceding (keratolytic) removal of the fungal feast.
  • Children
    • You should only use the preparation for infants and toddlers under medical monitoring.
    • Please make sure that no gel gets into the baby's mouth/toddler.

 

  • Wateriness and ability to operate machines
    • The gel has no or a negligible influence on the traffic and the ability to use machines.

Pregnancy

  • If you are pregnant or breastfeed, or if you suspect that you are pregnant or intend to become pregnant, ask your doctor or pharmacist for advice before using this drug.
  • Pregnancy
    • There is no sufficient data for the use of bifonazole in pregnant women.
    • Since Bifonazole is an active ingredient to be used exclusively on the skin and is therefore not to be expected with a systical effect (effect on other organs), a risk is not to be expected. Nevertheless, for precautionary reasons, Bifonazole should only be used during pregnancy after careful medical use risk assessment. In the first 3 months of pregnancy, the use of Bifonazole should be avoided.
  • Breastfeeding
    • Breastfeeding should be interrupted during treatment with Bifonazole.
    • There are no studies on the influence of bifonazole on fertility (fertility) of humans.

Hints

Read the package supplement and ask your doctor or pharmacist for risks and side effects.

Miscellaneous

- Carry out hygienic measures (e.g. regular laundry change)

Manufacturer:  DERMAPHARM AG, Lil-Dagover-Ring 7, 82031 Grünwald

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