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LEO Pharma

LEO Pharma
Cashel Road, Dublin 12,
Telephone: +353 1 490 8924
Fax: +353 1 708 2054
Medical Information e-mail: medical-info.ie@leo-pharma.com
Medical Information Facsimile: +353 1 708 2089


Summary of Product Characteristics last updated on medicines.ie: 29/09/2009
SPC Fucidin Cream

Table of Contents

  • 1. NAME OF THE MEDICINAL PRODUCT
  • 2. QUALITATIVE AND QUANTITATIVE COMPOSITION
  • 3. PHARMACEUTICAL FORM
  • 4. CLINICAL PARTICULARS
  • 4.1 Therapeutic indications
  • 4.2 Posology and method of administration
  • 4.3 Contraindications
  • 4.4 Special warnings and precautions for use
  • 4.5 Interaction with other medicinal products and other forms of interaction
  • 4.6 Pregnancy and lactation
  • 4.7 Effects on ability to drive and use machines
  • 4.8 Undesirable effects
  • 4.9 Overdose
  • 5. PHARMACOLOGICAL PROPERTIES
  • 5.1 Pharmacodynamic properties
  • 5.2 Pharmacokinetic properties
  • 5.3 Preclinical safety data
  • 6. PHARMACEUTICAL PARTICULARS
  • 6.1 List of excipients
  • 6.2 Incompatibilities
  • 6.3 Shelf life
  • 6.4 Special precautions for storage
  • 6.5 Nature and contents of container
  • 6.6 Special precautions for disposal and other handling
  • 7. MARKETING AUTHORISATION HOLDER
  • 8. MARKETING AUTHORISATION NUMBER(S)
  • 9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
  • 10. DATE OF REVISION OF THE TEXT


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1. NAME OF THE MEDICINAL PRODUCT

Fucidin® cream


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2. QUALITATIVE AND QUANTITATIVE COMPOSITION

Each gram of cream contains 20 mg fusidic acid.

For excipients, see section 6.1


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3. PHARMACEUTICAL FORM

Cream

A white, homogeneous cream.


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4. CLINICAL PARTICULARS

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4.1 Therapeutic indications

In the topical treatment of infections due to micro-organisms sensitive to this anti-infective, in particular Staphylococcus aureus.


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4.2 Posology and method of administration

Apply three to four times daily or as required.

Less frequent application may be adequate for covered lesions.


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4.3 Contraindications

Known hypersensitivity to fusidic acid/sodium fusidate or to any of the excipients.


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4.4 Special warnings and precautions for use

Fucidin®cream contains butylhydroxyanisole, cetyl alcohol and potassium sorbate which may cause local allergic skin reactions (e.g. contact dermatitis). In addition, butylhydroxyanisole may cause irritation to the eyes and the mucous membranes.

Bacterial resistance has been reported to occur with the use of fusidic acid. As with all antibiotics, extended or recurrent use may increase the risk of developing antibiotic resistance


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4.5 Interaction with other medicinal products and other forms of interaction

None known


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4.6 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 breast-feeding woman to fusidic acid is negligible. Fucidin®cream can be used during breast-feeding.


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4.7 Effects on ability to drive and use machines

Fucidin® administered topically has no or negligible influence on the ability to drive and to use machines.


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4.8 Undesirable effects
Very common >1/10
Common >1/100 and <1/10
Uncommon >1/1,000 and <1/100
Rare>1/10,000 and <1/1,000
Very rare<1/10,000

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 commonly reported adverse drug reactions are various skin reactions and in particular application site reactions. Allergic reactions have been reported.

Immune system disorders

Rare:

Allergic reaction

Skin and subcutaneous tissue disorders

Uncommon:

Rash*

Skin irritation

Pruritus

Rare:

Contact dermatitis

Urticaria

Angioneurotic oedema

Eczema

Periorbital oedema

Erythema

Skin burning sensation

Skin stinging sensation

*Various types of rash reactions such as erythematous, maculo-papular and pustular have been reported


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4.9 Overdose

Overdose is unlikey to occur.


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5. PHARMACOLOGICAL PROPERTIES

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5.1 Pharmacodynamic properties

ATC code: D06AX01

Fucidin® Cream contains fusidic acid a potent topical antibacterial. Fusidic acid and its salts exhibit fat and water solubility properties with strong surface activity, and show unusual ability to penetrate intact skin. Concentrations of 0.03 - 0.12 mcg/ml inhibit nearly all strains of Staphylococcus aureus. Topical Fucidin® is also active against Streptococci, Corynebacteria, Neisseria and certain Clostridia.


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5.2 Pharmacokinetic properties

There are no data which define the pharmacokinetics of Fucidin® Cream, following topical administration in man.

However, in vitro studies show that fusidic acid can penetrate intact human skin in concentrations well above the MIC-values of susceptible organisms. The degree of penetration depends on factors such as the duration of exposure to fusidic acid and the condition of the skin. Fusidic acid is excreted mainly in the bile with little excreted in the urine.


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5.3 Preclinical safety data

There are no preclinical data of relevance to the prescriber which are additional to that already included in other sections of the SPC.


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6. PHARMACEUTICAL PARTICULARS

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6.1 List of excipients

butylhydroxyanisole (E320)

cetyl alcohol

glycerol

liquid paraffin

polysorbate 60

potassium sorbate

purified water

white soft paraffin

hydrochloric acid


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6.2 Incompatibilities

Not applicable.


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6.3 Shelf life

3 years


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6.4 Special precautions for storage

Do not store above 30oC.


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6.5 Nature and contents of container

Internally lacquered aluminium tube, sealed with an aluminium membrane and fitted with a white polyethylene screw cap.

Contents: 15 g or 30 g cream.


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6.6 Special precautions for disposal and other handling

No special requirements.


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7. MARKETING AUTHORISATION HOLDER

LEO Laboratories Limited, Cashel Road, Dublin 12


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8. MARKETING AUTHORISATION NUMBER(S)

PA 46/4/12


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9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION

Date of first authorisation: 13 October 1980

Date of last renewal: 13 October 2005


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10. DATE OF REVISION OF THE TEXT

August 2009



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Active Ingredients

 
   Fusidic Acid

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Registered Number: 254776
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