Bactroban
Poland
Table of Contents
Package leaflet: Information for the user
Warning! Please keep this leaflet. The information on the immediate packaging is in a foreign language.
Bactroban (Bactroban 2%), 20 mg/g, nasal ointment
Mupirocin
Bactroban and Bactroban 2% are different trade names for the same medicine.
Please read the entire leaflet carefully before using the medicine, as it contains
important information for the patient.
- Keep this leaflet, as you may need to read it again.
- If you have any questions, please consult your doctor, pharmacist, or nurse.
- This medicine has been prescribed for a specific individual. Do not pass it on to others. It may harm someone else, even if their symptoms are the same.
- If the patient experiences any adverse reactions, including any not listed in this leaflet, inform the doctor, pharmacist, or nurse. See section 4.
Table of contents
- What Bactroban is and what it is used for
- Important information before using Bactroban
- How to use Bactroban
- Possible side effects
- How to store Bactroban
- Contents of the pack and other information
1. What Bactroban is and what it is used for
Bactroban nasal ointment (referred to as Bactroban in this leaflet) contains an antibiotic called mupirocin, in the form of mupirocin calcium.
It is used:
- to eliminate bacteria from the nose belonging to a group called staphylococci. This group includes MRSA (methicillin-resistant Staphylococcus aureus strains).
This ointment is intended for nasal use only.
2. Important information before using Bactroban
When not to use Bactroban
If the patient is allergic to mupirocin or to any of the other ingredients of Bactroban
(listed in section 6).
If in doubt about the use of the medicine, consult a doctor or pharmacist.
Warnings and precautions
- Do not use in newborns and infants.
- Do not apply Bactroban ointment to the eyes or near the eyes. Avoid contact with the eyes. If the ointment gets into the eye, rinse thoroughly with water until all traces of the ointment are removed.
- Do not apply Bactroban to the mouth or swallow it.
Bactroban and other medicines
Inform your doctor or pharmacist about all medicines you are currently taking or have recently taken, including those obtained without a prescription, herbal medicines, and any medicines you plan to take.
Pregnancy and breastfeeding
If the patient is pregnant or breastfeeding, suspects she may be pregnant, or is planning to have a child, she should consult a doctor or pharmacist before using this medicine.
3. How to use Bactroban
This medicine should always be used as directed by a doctor or pharmacist. If you have any doubts,
consult your doctor or pharmacist.
How to use the medicine
Bactroban should be applied into the nose twice daily.
- Wash and dry your hands.
- Squeeze a small amount of ointment, about the size of a match head, onto your little finger.
- Apply inside one nostril.
- Repeat steps 2 and 3 for the other nostril.
- Press the sides of the nose together and gently press to evenly spread the ointment within the nostrils.
- Replace the cap on the tube and wash your hands.
Small children and elderly patients
Instead of using the little finger, cosmetic swabs may be used to apply Bactroban into the nose.
Particular caution should be exercised in these patients. Bactroban should not be used in newborns and infants.
How long to use Bactroban
Continue using Bactroban for as long as directed by your doctor. If in doubt, consult your doctor or pharmacist.
Usually, bacteria in the nose are eliminated within 3–5 days after starting treatment.
Do not use Bactroban for longer than 10 days.
Use of more than the recommended dose of Bactroban
If more Bactroban than recommended has been used, contact your doctor or pharmacist. Carefully remove any excess ointment.
If Bactroban has been swallowed, contact your doctor immediately and inform them what and how much has been ingested.
Missed dose of Bactroban
If a dose is missed, apply the medicine as soon as you remember. If the next dose is due within one hour, skip the missed dose.
Do not use a double dose to make up for a missed dose.
Stopping Bactroban treatment
If Bactroban treatment is stopped too early, not all bacteria may be eliminated and they may continue to multiply.
Ask your doctor or pharmacist when to stop using the ointment.
If you have any doubts about how to use this medicine, consult your doctor or pharmacist.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The following are side effects that may occur with this medicine.
Uncommon (may occur in 1 in 100 to 1 in 1000 patients):
- itching, redness, burning, tingling or stinging in the nose,
- nasal discharge.
Very rare (may occur in fewer than 1 in 10,000 patients):
- skin hypersensitivity reactions (rash, itching, redness, pain),
- systemic allergic reactions, such as:
- generalized rash, urticaria,
- angioedema (swelling, sometimes affecting the face and lips, which may lead to breathing difficulties),
- fainting or loss of consciousness → if any of these symptoms occur, discontinue use of the medicine and contact a doctor immediately.
If skin irritation or hypersensitivity occurs
- remove the ointment from the skin,
- stop using the medicine,
- inform the doctor as quickly as possible.
In rare cases, medicines such as Bactroban nasal ointment may cause inflammation of the colon (large intestine) – presenting as diarrhoea, usually bloody and containing mucus, abdominal pain, and fever ( pseudomembranous colitis ).
If any of the above symptoms occur, contact a doctor as quickly as possible.
Reporting of side effects
If any adverse reactions occur, including any adverse reactions not listed in this leaflet, inform your doctor, pharmacist or nurse. Side effects can also be reported directly to the Department of Monitoring Adverse Drug Reactions, 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
Reporting side effects helps to provide more information on the safety of the medicine.
5. How to store Bactroban
Keep this medicine out of 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 indicated.
Do not use Bactroban if it looks different from normal (see description in section 6).
Medicines must not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer in use. This will help protect the environment.
6. Contents of the packaging and other information
What Bactroban contains
- The active substance is mupirocin as mupirocin calcium. Each gram of nasal ointment contains 20 mg (2%) of mupirocin. A 3 g tube contains 60 mg of mupirocin.
- The other ingredients are: vaseline, Softisan 649.
What Bactroban looks like and contents of the pack
Bactroban is a white, homogenous ointment. The medicine is available in aluminium tubes containing 3 g of ointment, packed in a cardboard box.
For more detailed information, please contact the Marketing Authorisation Holder or the Parallel Importer.
Marketing Authorisation Holder in France, country of export:
Laboratoire GlaxoSmithKline, 23, rue François Jacob, 92500 Rueil-Malmaison, France
Manufacturer:
GlaxoSmithKline Trading Services Limited, 12 Riverwalk, Citywest Business Campus, Dublin 24, Ireland
Delpharm Poznań Spółka Akcyjna, Grunwaldzka 189, 60-322 Poznań, Poland
Parallel Importer:
Delfarma Sp. z o.o., Św. Teresy od Dzieciątka Jezus 111, 91-222 Łódź, Poland
Repackaged by:
Delfarma Sp. z o.o., Św. Teresy od Dzieciątka Jezus 111, 91-222 Łódź, Poland
Marketing Authorisation numbers in France, country of export: 34009 363 416 5 4
34009 363 417 1 5
Parallel Import Licence Number: 101/23