Bactroban(Bactroban 2 %)
Mupirocin
Bactroban and Bactroban 2 % are different trade names for the same medicine.
Bactroban nasal ointment (referred to as Bactroban in this leaflet) contains the antibiotic mupirocin in the form of mupirocin calcium.
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.
If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a child, consult your doctor or pharmacist before using this medicine.
Always use this medicine exactly as your doctor or pharmacist has told you. If you are unsure, consult your doctor or pharmacist.
Bactroban should be applied to the nose 2 times a day.
Instead of using the little finger to apply the medicine to the nose, 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 prescribed. 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, consult your doctor or pharmacist. Carefully remove any excess ointment.
If you swallow Bactroban, contact your doctor immediately and inform them of what and how much you have swallowed.
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 missed dose.
If you stop using Bactroban too early, not all the bacteria may be killed or they may continue to multiply. 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:
Very Rare(may occur in less than 1 in 10,000 patients):
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, inform your doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products, Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych, 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.
Do not store above 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 section 6).
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Bactroban is a white ointment with a uniform consistency. The medicine is available in a 3 g aluminum tube in a cardboard box.
For more detailed information, consult the marketing authorization holder or parallel importer.
Laboratoire GlaxoSmithKline
23, rue François Jacob
92500 Rueil-Malmaison
France
GlaxoSmithKline Trading Services Limited
12 Riverwalk,
Citywest Business Campus
Dublin 24
Ireland
GlaxoSmithKline Pharmaceuticals S.A.
ul. Grunwaldzka 189
60-322 Poznań
InPharm Sp. z o. o.
ul. Strumykowa 28/11
03-138 Warsaw
InPharm Sp. z o.o. Services sp. k.
ul. Chełmżyńska 249
04-458 Warsaw
Authorization Number in France, the Country of Export:3400936341654
363416-5
[Information about the Trademark]
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