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Package Leaflet: Information for the User
Tobramycin SUN 300 mg/5 ml Solution for Inhalation by Nebulizer
tobramycin
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
Contents of the pack
Tobramycin SUN contains an antibiotic medicine called tobramycin. This belongs to a class of antibiotic medicines called aminoglycosides.
Antibiotics are used to treat bacterial infections and will not work for viral infections such as the common cold or flu.
It is important that you follow the instructions regarding the dose, administration interval, and duration of treatment as indicated by your doctor.
Do not store or reuse this medicine. If you have any leftover antibiotic after finishing treatment, return it to the pharmacy for proper disposal. Do not throw away medicines via wastewater or household waste.
Tobramycin SUN is used in patients aged 6 years and older who have cystic fibrosis, for the treatment of lung infections caused by a bacterium called Pseudomonas aeruginosa.
Tobramycin SUN combats the infection caused by the Pseudomonasbacterium in your lungs and helps improve your breathing.
When you inhale Tobramycin SUN, the antibiotic goes directly to your lungs to fight the bacteria that cause the infection. For better results with this medicine, follow the instructions in this leaflet.
What is Pseudomonas aeruginosa?
It is a very common bacterium that infects almost all patients with cystic fibrosis at some point in their lives. Some of them do not get this infection until very late in life, while others get it very young.
This bacterium is one of the most damaging to people with cystic fibrosis. If the infection is not properly controlled, it can continue to damage your lungs, causing additional breathing problems.
Tobramycin SUN kills the bacteria that cause lung infections. This infection can be successfully controlled if the problem is addressed at an early stage.
Do not use Tobramycin SUN:
If any of the above cases apply to you, do not take this medicine and consult your doctor.
Warnings and precautions
Consult your doctor before starting to use Tobramycin SUN if you suffer from or have ever suffered from any of the following conditions:
If any of these cases apply to you, inform your doctor before using Tobramycin SUN.
Inhaling medicines can cause chest tightness and wheezing, and this can occur with Tobramycin SUN. Your doctor will supervise your first dose of Tobramycin SUN and check your lung function before and after the dose. If you are not doing so, your doctor may have you use a bronchodilator (e.g., salbutamol) before using Tobramycin SUN.
If you are using Tobramycin SUN, Pseudomonasstrains may become resistant to treatment over time. This means that over time, the medicine may not work as well as it should. Consult your doctor if you are concerned about this.
If tobramycin is administered by injection, it can occasionally cause hearing loss, dizziness, and kidney damage, and may harm the fetus.
Children and adolescents
Tobramycin SUN can be administered to children and adolescents from 6 years of age. Tobramycin SUN should not be administered to children under 6 years of age.
Elderly
If you are 65 years of age or older, your doctor may perform additional tests to decide if Tobramycin SUN is a suitable treatment for you.
Other medicines and Tobramycin SUN
Tell your doctor or pharmacist if you are using, have recently used, or might use any other medicines.
DO NOTtake the following medicines while using Tobramycin SUN:
The following medicines may increase the risk of harmful effects if administered while you are receiving injectionsof tobramycin:
If you are taking one or more of the above medicines, discuss this with your doctor before using Tobramycin SUN.
Do not mix or dilute Tobramycin SUN with any other medicine in your nebulizer.
If you are taking several different treatments for cystic fibrosis, you should take them in the following order:
Also, check this order with your doctor.
Pregnancy and breastfeeding
Pregnancy
If you are pregnant, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before using this medicine.
It is not known if inhaling this medicine during pregnancy causes adverse effects. When administered by injection, tobramycin and other aminoglycoside antibiotics can cause harm to the fetus, such as deafness.
Breastfeeding
If you are breastfeeding, ask your doctor for advice before using any medicine.
Driving and using machines
Tobramycin SUN should not affect your ability to drive and use machines.
Follow the instructions for administration of this medicine exactly as indicated by your doctor. If in doubt, consult your doctor again.
The recommended dose is twoampoules per day (one in the morning and one in the evening) for 28 days.
With Tobramycin SUN | Without Tobramycin SUN |
Take Tobramycin SUN twice a day, every day for 28 days | Do not take Tobramycin SUN for the next 28 days |
Repeat the cycle
Continue using Tobramycin SUN with this cyclical pattern for the time indicated by your doctor. If you have any doubts about the duration of treatment with Tobramycin SUN, consult your doctor or pharmacist.
Instructions for use of Tobramycin SUN
This part of the leaflet explains how to use, care for, and handle Tobramycin SUN. Read and follow these instructions carefully.
If you have any additional questions about the use of this medicine, consult your doctor or pharmacist.
The equipment you need to inhale Tobramycin SUN
Tobramycin SUN must be used with a reusable, clean, and dry nebulizer.
The LC PLUS nebulizer (manufactured by PARI GmbH) is suitable for use with Tobramycin SUN.
Your doctor or physiotherapist may advise you on the correct use of Tobramycin SUN and the equipment you need. You may need different nebulizers for your other inhaled medicines for cystic fibrosis.
Preparing Tobramycin SUN for inhalation
Using Tobramycin SUN with LC PLUS (PARI GmbH)
If you want to obtain more detailed instructions on the use and care of the nebulizer, consult the leaflet that comes with the PARI LC PLUS.



If you are interrupted or need to cough or rest during administration, turn off the compressor to avoid wasting the medicine.
Turn the compressor back on when you are ready to restart the treatment. Omit this dose if your next dose is due in less than 6 hours.
If you use more Tobramycin SUN than you should
If you inhale too much Tobramycin SUN, your voice may become very hoarse. Make sure to inform your doctor as soon as possible. If you swallow Tobramycin SUN, inform your doctor as soon as possible.
If you forget to use Tobramycin SUN
If you forget to use Tobramycin SUN and it is at least 6 hours until your next dose, take a dose as soon as possible. Otherwise, wait for your next dose. Do not take a double dose to make up for forgotten doses.
If you stop treatment with Tobramycin SUN
Do not stop using Tobramycin SUN unless your doctor tells you to, as the lung infection may not be properly controlled and may worsen.
If you have any additional questions about the use of this medicine, consult your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Serious side effects
Stop using Tobramycin SUN and tell your doctor immediatelyif you experience any of the following side effects:
Tell your doctor immediatelyif you experience any of the following side effects:
Your underlying lung disease may worsen while you are using Tobramycin SUN. This may be due to lack of efficacy. Tell your doctor immediately if this happens.
Other side effects
Tell your doctor as soon as possible if you experience any of the following side effects:
Very common (may affect more than 1 in 10 people)
Common (may affect up to 1 in 10 people)
Other side effects
Frequency not known (cannot be estimated from the available data)
If you have received Tobramycin SUN at the same time or after repeated cycles of tobramycin or other aminoglycoside antibiotics by injection, hearing loss has been reported as a side effect.
Injections of tobramycin or other aminoglycosides can cause allergic reactions, hearing problems, and kidney problems.
Patients with cystic fibrosis have various symptoms of the disease. These may even occur while taking Tobramycin SUN, but they should not be more frequent or seem worse than before treatment.
Reporting of side effects
If you experience any side effects, talk to your doctor, pharmacist, or nurse, even if it is possible side effects not listed in this leaflet. You can also report side effects directly through the Spanish Pharmacovigilance System for Human Use Medicines: www.notificaRAM.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use Tobramicina SUN after the expiry date which is stated on the packaging, on the bag, or printed on the ampoule after CAD. The expiry date is the last day of the month indicated.
Store in a refrigerator (between 2°C and 8°C). If you do not have a refrigerator (for example, during transportation of the medicine), you can keep the aluminum bags (opened or closed) at room temperature (not above 25°C) for a maximum of 28 days. Do not use the Tobramicina SUN ampoules if you have stored them at room temperature for more than 28 days.
Keep the ampoules in the original packaging to protect them from light. This medicine is usually colorless to light yellow, but the color may vary and sometimes may be dark yellow. This does not affect the activity of this medicine, as long as the storage instructions are followed.
Do not use this medicine if you notice that it becomes cloudy or if there are particles in the solution.
Never store an opened ampoule. Once an ampoule is opened, it must be used immediately and any remaining product must be discarded.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of the packaging and medicines that are no longer needed. This will help protect the environment.
Composition of Tobramicina SUN
Appearance of the Product and Package Contents
Tobramicina SUN solution for inhalation by nebulizer is a clear, colorless to light yellow solution without visible particles.
Tobramicina SUN is presented in a ready-to-use ampoule. The ampoules are packaged in aluminum bags, one aluminum bag contains 4 ampoules corresponding to 2 days of treatment.
Tobramicina SUN is available in packages of 56, 112, or 168 ampoules, which are sufficient for one, two, or three treatment cycles, respectively.
Only some package sizes may be marketed.
Marketing Authorization Holder
Sun Pharmaceutical Industries Europe BV
Polarisavenue 87
2132 JH Hoofddorp
Netherlands
Manufacturer
Sun Pharmaceutical Industries Europe BV
Polarisavenue 87
2132 JH Hoofddorp
Netherlands
Terapia SA
Str. Fabricii Nr. 124
400632, Cluj-Napoca
Romania
You can request more information about this medicine by contacting the local representative of the marketing authorization holder:
Local Representative
Sun Pharma Laboratorios, S.L.
Rambla de Catalunya, 53-55
08007 Barcelona
Spain
Tel: +34 93 342 78 90
This medicine is authorized in the Member States of the European Economic Area and in the United Kingdom (Northern Ireland) under the following names
Germany: Tobramycin SUN 300 mg Lösung für einen Vernebler
Denmark: Tobramycin SUN 300 mg/5 ml inhalationsvæske til nebulisator, opløsning
Spain: Tobramicina SUN 300 mg/5 ml solución para inhalación por nebulizador
France: Tobramycine SUN 300 mg/5 ml solution pour inhalation par nébuliseur
Italy: Tobramicina SUN 300 mg/5 ml soluzione per nebulizzatore
Netherlands: Tobramycine SUN 300 mg/5 ml verneveloplossing
Poland: Tobramycyna SUN 300 mg/5 ml roztwór do nebulizacji
Romania: Tobramicina SUN 300 mg/5 ml solutie pentru nebulizator
United Kingdom
(Northern Ireland): Tobramycin 300 mg/5 ml nebuliser solution
Date of the last revision of this leaflet: September 2021
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