Mupirocin
Bactroban nasal ointment (referred to as Bactroban in this leaflet) contains the antibiotic mupirocin in the form of mupirocin calcium (micronized).
It is used:
This ointment is intended for use in the nose only.
If the patient is allergic to mupirocin or any of the other ingredients of Bactroban (listed in section 6).
In case of doubts related to the use of the medicine, consult a doctor or pharmacist.
Tell your doctor or pharmacist about all medicines you are currently taking or have recently taken, including those that are available without a prescription and herbal medicines, as well as any medicines you plan to take.
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If the patient is pregnant or breastfeeding, thinks she may be pregnant, or plans to have a child, she should consult a doctor or pharmacist before using this medicine.
Always use this medicine exactly as your doctor or pharmacist has told you. If you are not sure, consult your doctor or pharmacist.
Use Bactroban twice a dayin the nose.
Instead of using the little finger to apply the medicine, you can use a cotton swab.
Special precautions should be taken with these patients. Bactroban should not be used in newborns and infants.
Use Bactroban for as long as your doctor has told you. If you are unsure, consult your doctor or pharmacist. The bacteria in the nose usually die after 3-5 days of treatment.
Do not use Bactroban for more than 10 days.
If you use more Bactroban than you should, contact your doctor or pharmacist. Carefully remove any excess ointment.
If you swallow Bactroban, contact your doctor immediately and tell them how much you have taken.
If you forget to use your medicine, use it as soon as you remember. If it is almost time for your next dose, skip the missed dose.
Do not use a double dose to make up for a forgotten dose.
If you stop using Bactroban too soon, not all the bacteria may be killed or they may multiply again. Ask your doctor or pharmacist when to stop using the ointment.
If you have any doubts about using the medicine, consult your doctor or pharmacist.
Like all medicines, Bactroban can cause side effects, although not everybody gets them.
The following side effects may occur:
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Very rare(may affect up to 1 in 10,000 people):
In rare cases, medicines like Bactroban nasal ointment may cause colitis (inflammation of the colon) - characterized by the onset of diarrhea, usually bloody and containing mucus, abdominal pain, and fever ( pseudomembranous colitis).
If you experience any of these symptoms, contact your doctor as soon as possible.
If you experience any side effects, including any side effects not listed in this leaflet, tell your doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: + 48 22 49 21 301, fax: + 48 22 49 21 309, website: https://smz.ezdrowie.gov.pl
By reporting side effects, you can help provide more information on the safety of this medicine.
Keep the medicine out of the sight and reach of children.
Store in a temperature below 25°C.
Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the month.
Do not use Bactroban if it looks different from normal (see description in point 6).
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
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Bactroban is a white ointment with a uniform consistency. The medicine is available in aluminum tubes containing 3 g of ointment, in a cardboard box.
For more detailed information, consult the marketing authorization holder or parallel importer.
GlaxoSmithKline Monoprosopi Α.Ε.Β.Ε.
Kifisias Ave 266
152 32 Chalandri
Greece
GlaxoSmithKline Pharmaceuticals S.A., ul. Grunwaldzka 189, 60-322 Poznań, Poland
GlaxoSmithKline Trading Services Limited, 12 Riverwalk, Citywest Business Campus, Dublin 24,
Ireland
Delfarma Sp. z o.o., ul. Św. Teresy od Dzieciątka Jezus 111, 91-222 Łódź
Delfarma Sp. z o.o., ul. Św. Teresy od Dzieciątka Jezus 111, 91-222 Łódź
License number in Greece, the country of export: 41679/10-9-2009
50770/04-07-2013
11795/26-3-2019
[Information about the trademark]
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Need help understanding this medicine or your symptoms? Online doctors can answer your questions and offer guidance.