FUCICORT Cream Ref.[50937] Active ingredients: Betamethasone Fusidic acid

Source: Medicines and Medical Devices Safety Authority (NZ)  Revision Year: 2019  Publisher: LEO Pharma Ltd, Auckland, New Zealand, Ph: 0800 497 456

4.1. Therapeutic indications

Fucicort is indicated in inflammatory dermatoses where bacterial infection is present or likely to occur. Inflammatory dermatoses include atopic eczema, discoid eczema, seborrheic dermatitis, contact dermatitis, lichen simplex chronicus, psoriasis, discoid lupus erythematosus.

4.2. Posology and method of administration

Uncovered lesions

A small quantity should be applied to the affected area twice daily until a satisfactory response is obtained. A single treatment course should not normally exceed 2 weeks.

Covered lesions

In the more resistant lesions the effect of Fucicort cream can be enhanced by occlusion with polyethylene film. Overnight occlusion is usually adequate.

4.9. Overdose

For topically applied fusidic acid, no information concerning potential symptoms and signs due to overdose administration is available. Cushing’s syndrome and adrenocortical insufficiency may develop following topical application of corticosteroids in large amounts and for more than three weeks.

Systemic consequences of an overdose of the active substances after accidental oral intake are unlikely to occur. The amount of fusidic acid in one tube of Fucicort does not exceed the oral daily dose of systemic treatment. A single oral overdose of corticosteroids is rarely a clinical problem.

For advice on the management of overdose please contact the National Poisons Centre 0800 POISON (0800 764 766).

6.3. Shelf life

3 years.

6.4. Special precautions for storage

Store at or below 30°C.

6.5. Nature and contents of container

15 g.

6.6. Special precautions for disposal and other handling

Any unused medicine or waste material should be disposed of in accordance with local
legislation.

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