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  • Fucidin Cream
    / Dexcel


    Active Ingredient
    Fusidic Acid 20 mg/g

    Status in Israel
    RX

    Presentation and Status in Health Basket

    Presentation Basket Yarpa Pharmasoft

    Cream

    30 gr

    partial basket chart 69964 6385

    Dosage

    Apply three to four times daily or as required. Less frequent application may be adequate for covered lesions.


    Indications

    Local treatment of skin infections due to sensitive strains of staphylococus aureus.


    Contra-Indications

    Known hypersensitivity to fusidic acid/sodium fusidate or to any of the excipients.
    See prescribing information for full details.


    Special Precautions

    This drug contains butylhydroxyanisole, potassium sorbate and cetyl alcohol which may cause local allergic skin reactions (e.g. contact dermatitis). In addition, butylhydroxyanisole may cause irritation to the eyes and the mucous membranes.
    See prescribing information for full details.


    Side Effects

    Based on combined clinical data for Fucidin cream and Fucidin ointment, approximately 5% of patients can be expected to experience an undesirable effect. The most frequently reported adverse drug reactions are various skin reactions and in particular application site reactions. Allergic reactions and contact dermatitis have been reported. Undesirable effects are listed by MedDRA SOC and the individual undesirable effects are listed starting with the most frequently reported.
    Immune system disorders: Rare (≥1/10,000 and <1/1,000): Allergic reaction.
    Eye Disorders: Rare (≥1/10,000 and <1/1,000): Conjunctival irritation.
    Skin and subcutaneous tissue disorders: Uncommon (≥1/1,000 and  <1/100): Rash*, Irritation at site of application (incl. pain, stinging, burning and erythema), Pruritus, Contact dermatitis
    * Various types of rash reactions such as erythematous, maculo-papular and pustular have been reported.
    Frequency unknown: Urticaria, Angioneurotic oedema, Eczema, Periorbital oedema.
    See prescribing information for full details.


    Drug interactions

    None known.


    Pregnancy and Lactation

    Pregnancy: For fusidic acid/sodium fusidate no clinical data on exposed pregnancies are available. Animal studies do not indicate a direct or indirect harmful effect with respect to pregnancies, embryonal/foetal development, parturition or postnatal development. Caution should be exercised when prescribing to pregnant women.
    Lactation: No effect on the suckling child are anticipated since the systemic exposure of the breastfeeding woman to fusidic acid is negligible. This cream and ointment can be used during breast-feeding.

     


    Overdose

    Overdose is unlikely to occur.


    Manufacturer
    LEO Pharmaceutical Products Ltd.
    Licence holder
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