Wednesday, 28 September 2016

Bactroban 2% Cream





1. Name Of The Medicinal Product



Bactroban® 2% Cream.


2. Qualitative And Quantitative Composition



1g Cream contains: 21.5mg Mupirocin calcium equivalent to 20.0mg mupirocin.



For excipients, see Section 6.1.



3. Pharmaceutical Form



Cream.



Bactroban Cream is presented as a white cream of homogeneous appearance.



4. Clinical Particulars



4.1 Therapeutic Indications



Bactroban Cream is indicated for the topical treatment of secondarily infected traumatic lesions such as small lacerations, sutured wounds or abrasions (up to 10cm in length or 100cm2 in area), due to susceptible strains of Staphylococcus aureus and Streptococcus pyogenes.



4.2 Posology And Method Of Administration



Dosage



Adults/children/elderly



Three times a day for up to 10 days, depending on the response.



Patients not showing a clinical response within 3 to 5 days should be re-evaluated.



The duration of treatment should not exceed 10 days.



Children < 1 year



Mupirocin Cream has not been studied in infants under 1 year old and therefore it should not be used in these patients until further data become available.



Hepatic impairment: No dosage adjustment is necessary.



Renal impairment: No dosage adjustment is necessary.



Method of administration



A thin layer of cream should be applied to the affected area with a piece of clean cotton wool or gauze swab.



The treated area may be covered by a dressing.



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



4.3 Contraindications



Hypersensitivity to mupirocin or any of the excipients (see section 6.1).



4.4 Special Warnings And Precautions For Use



Should a possible sensitisation reaction or severe local irritation occur with the use of Bactroban Cream, treatment should be discontinued, the product should be washed off and appropriate therapy instituted.



As with other antibacterial products, prolonged use may result in overgrowth of non-susceptible organisms.



Bactroban Cream formulation is not suitable for intranasal use. For intranasal use, a separate presentation, Bactroban nasal ointment, is available.



Avoid contact with the eyes. If contaminated, the eyes should be thoroughly irrigated with water until the cream residues have been removed.



Bactroban Cream contains cetyl alcohol and stearyl alcohol. These inactive ingredients may cause local skin reactions (e.g. contact dermatitis).



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



No drug interactions have been identified.



4.6 Pregnancy And Lactation



Use in pregnancy:



Reproduction studies on mupirocin in animals have revealed no evidence of harm to the foetus. As there is no clinical experience on its use during pregnancy, mupirocin should only be used in pregnancy when the potential benefits outweigh the possible risks of treatment.



Use in lactation:



There is no information on the excretion of mupirocin in milk. If a cracked nipple is to be treated, it should be thoroughly washed prior to breast feeding.



4.7 Effects On Ability To Drive And Use Machines



No adverse effects on the ability to drive or operate machinery have been identified.



4.8 Undesirable Effects



Data from clinical trials was used to determine the frequency of very common to rare undesirable effects.



The following convention has been used for the classification of frequency:-



very common >1/10, common >1/100 and <1/10 , uncommon >1/1000 and <1/100,



rare >1/10,000 and <1/1000 , very rare <1/10,000.



Skin and subcutaneous tissue disorders:



Common: Application site hypersensitivity reactions including urticaria, pruritus, erythema, burning sensation, contact dermatitis, rash



Skin dryness and erythema have been reported in irritancy studies in volunteers.



4.9 Overdose



The toxicity of mupirocin is very low. In the event of accidental ingestion of the cream symptomatic treatment should be given.



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



ATC classification



Properties



ATC-code : D06A X09, Antibiotics and chemotherapeutics for dermatological use.



Mode of Action



Mupirocin is an antibiotic produced through fermentation by Pseudomonas fluorescens. Mupirocin inhibits isoleucyl transfer-RNA synthetase, thereby arresting bacterial protein synthesis. Due to this particular mode of action and its unique chemical structure, mupirocin does not show any cross-resistance with other clinically available antibiotics.



Mupirocin has bacteriostatic properties at minimum inhibitory concentrations and bactericidal properties at the higher concentrations reached when applied locally.



Activity



Mupirocin is a topical antibacterial agent showing in vivo activity against Staphylococcus aureus (including methicillin-resistant strains), S. epidermidis and beta-haemolytic Streptococcus species.



The in-vitro spectrum of activity includes but is not limited to the following bacteria which are most often implicated in skin infections:



- Staphylococcus aureus (including beta-lactamase-producing strains and methicillin resistant strains).



- Staphylococcus epidermidis (including beta-lactamase-producing strains and methicillin-resistant strains).



- Other coagulase-negative staphylococci (including methicillin-resistant strains).



- Streptococcus species.



5.2 Pharmacokinetic Properties



Absorption



Systemic absorption of mupirocin through intact human skin is low although it may occur through broken/diseased skin. However, clinical trials have shown that when given systemically, it is metabolised to the microbiologically inactive metabolite monic acid and rapidly excreted.



Excretion



Mupirocin is rapidly eliminated from the body by metabolism to its inactive metabolite monic acid which is rapidly excreted by the kidney.



5.3 Preclinical Safety Data



Pre-clinical effects were seen only at exposures which give no cause for concern for man under normal conditions of clinical use. Mutagenicity studies revealed no risks to man.



6. Pharmaceutical Particulars



6.1 List Of Excipients



Xanthan gum, liquid paraffin, cetomacrogol 1000, stearyl alcohol, cetyl alcohol, phenoxyethanol, benzyl alcohol, purified water.



6.2 Incompatibilities



None known



6.3 Shelf Life



18 months



6.4 Special Precautions For Storage



Do not store above 25°C. Do not freeze.



6.5 Nature And Contents Of Container



Squeezable aluminium tubes with a screw cap containing 15 g of white cream.



6.6 Special Precautions For Disposal And Other Handling



Any product remaining at the end of treatment should be discarded.



Administrative Data


7. Marketing Authorisation Holder



Beecham Group plc



980 Great West Road, Brentford



Middlesex TW8 9GS



Trading as:



GlaxoSmithKline UK



Stockley Park West,



Uxbridge,



Middlesex, UB11 1BT



8. Marketing Authorisation Number(S)



PL 00038/0372



9. Date Of First Authorisation/Renewal Of The Authorisation



28 October 1998



10. Date Of Revision Of The Text



8th March 2010



11. Legal category


POM




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