GlaxoSmithKline UK

Stockley Park West, Uxbridge, Middlesex, UB11 1BT
Telephone: +44 (0)800 221 441
Fax: +44 (0)208 990 4328
Medical Information e-mail: customercontactuk@gsk.com

Summary of Product Characteristics last updated on the eMC: 04/06/2008
SPC Bactroban Ointment


Go to top of the page
1. NAME OF THE MEDICINAL PRODUCT

Bactroban® Ointment


Go to top of the page
2. QUALITATIVE AND QUANTITATIVE COMPOSITION

Mupirocin 2.0% w/w


Go to top of the page
3. PHARMACEUTICAL FORM

Ointment in a white, translucent, water-soluble, polyethylene glycol base. For topical administration.


Go to top of the page
4. CLINICAL PARTICULARS

Go to top of the page
4.1 Therapeutic indications

Bactroban is a topical antibacterial agent, active against those organisms responsible for the majority of skin infections, e.g. Staphylococcus aureus, including methicillin-resistant strains, other staphylococci, streptococci. It is also active against Gram-negative organisms such as Escherichia coli and Haemophilus influenzae. Bactroban Ointment is used for skin infections, e.g. impetigo, folliculitis, furunculosis.


Go to top of the page
4.2 Posology and method of administration

Dosage:

Adults (including elderly) and children:

Bactroban Ointment should be applied to the affected area up to three times a day for up to 10 days.

The area may be covered with a dressing or occluded if desired.

Administration:

Topical.

Do not mix with other preparations as there is a risk of dilution, resulting in a reduction of the antibacterial activity and potential loss of stability of the mupirocin in the ointment.


Go to top of the page
4.3 Contraindications

Bactroban ointment should not be given to patients with a history of hypersensitivity to any of its constituents.

This Bactroban Ointment formulation is not suitable for ophthalmic or intranasal use.


Go to top of the page
4.4 Special warnings and precautions for use

When Bactroban Ointment is used on the face, care should be taken to avoid the eyes.

Polyethylene glycol can be absorbed from open wounds and damaged skin and is excreted by the kidneys. In common with other polyethylene glycol-based ointments, Bactroban Ointment should be used with caution if there is evidence of moderate or severe renal impairment.

In the rare event of a possible sensitisation reaction or severe local irritation occurring with the use of Bactroban ointment, treatment should be discontinued, the product should be rinsed off and appropriate alternative therapy for the infection instituted.


Go to top of the page
4.5 Interaction with other medicinal products and other forms of interaction

None stated.


Go to top of the page
4.6 Pregnancy and lactation

This product should not be used during pregnancy and lactation unless considered essential by the physician.

Pregnancy: Adequate human data on use during pregnancy are not available. However animal studies have not identified any risk to pregnancy or embryo-foetal development.

Lactation: Adequate human and animal data on use during lactation are not available.


Go to top of the page
4.7 Effects on ability to drive and use machines

None stated.


Go to top of the page
4.8 Undesirable effects

Adverse reactions are listed below by system organ class and frequency. Frequencies are defined as: very common (GREATER-THAN OR EQUAL TO (8805)1/10), common (GREATER-THAN OR EQUAL TO (8805)1/100, <1/10), uncommon (GREATER-THAN OR EQUAL TO (8805)1/1000, <1/100), rare (GREATER-THAN OR EQUAL TO (8805)1/10,000, <1/1000), very rare (<1/10,000), including isolated reports. Common and uncommon adverse reactions were determined from pooled safety data from a clinical trial population of 1573 treated patients encompassing 12 clinical studies. Very rare adverse reactions were primarily determined from post-marketing experience data and therefore refer to reporting rate rather than true frequency.

Immune system disorders:

Very rare: Systemic allergic reactions have been reported with Bactroban Ointment.

Skin and subcutaneous tissue disorders:

Common: Burning localised to the area of application.

Uncommon: Itching, erythema, stinging and dryness localised to the area of application.

Uncommon: Cutaneous sensitisation reactions to mupirocin or the ointment base.


Go to top of the page
4.9 Overdose

The toxicity of mupirocin is very low. In the event of overdose, symptomatic treatment should be given.


Go to top of the page
5. PHARMACOLOGICAL PROPERTIES

Go to top of the page
5.1 Pharmacodynamic properties

Bactroban (mupirocin) potently inhibits bacterial protein and RNA synthesis by inhibition of isoleucyl-transfer RNA synthetase.


Go to top of the page
5.2 Pharmacokinetic properties

After topical application of Bactroban Ointment, mupirocin is only very minimally absorbed systemically and that which is absorbed is rapidly metabolised to the antimicrobially inactive metabolite, monic acid. Penetration of mupirocin into the deeper epidermal and dermal layers of the skin is enhanced in traumatised skin and under occlusive dressings.


Go to top of the page
5.3 Preclinical safety data

None stated.


Go to top of the page
6. PHARMACEUTICAL PARTICULARS

Go to top of the page
6.1 List of excipients

Polyethylene Glycol 400 USNF

Polyethylene Glycol 3350 USNF


Go to top of the page
6.2 Incompatibilities

None stated.


Go to top of the page
6.3 Shelf life

Bactroban Ointment has a shelf-life of two years.


Go to top of the page
6.4 Special precautions for storage

Store at room temperature (below 25°C).


Go to top of the page
6.5 Nature and contents of container

Original pack of 5 and 15 g* (sealed tube in a carton) with Patient Information Leaflet.


Go to top of the page
6.6 Special precautions for disposal and other handling

No special instructions.


Go to top of the page
Administrative Data

Go to top of the page
7. MARKETING AUTHORISATION HOLDER

Beecham Group plc

980 Great West Road,

Brentford,

Middlesex TW8 9GS

Trading as:

GlaxoSmithKine UK,

Stockley Park West,

Uxbridge,

Middlesex UB11 1BT


Go to top of the page
8. MARKETING AUTHORISATION NUMBER(S)

PL 00038/0319


Go to top of the page
9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION

21 May 2008


Go to top of the page
10. DATE OF REVISION OF THE TEXT

21 May 2008


Go to top of the page
11. Legal Status

POM

* At time of printing only the details relevant to marketed packs will be included.



More information about this product

Link to this document from your website: http://emc.medicines.org.uk/medicine/2028/SPC/Bactroban Ointment/

Active Ingredients/Generics

 
   mupirocin


© 2009 Datapharm Communications Ltd

Go to www.medicines.org.uk