Prospecto: information for the patient
Tobrabact 3.0 mg/ml eye drops solution.
tobramycin
Read the entire prospect carefully before starting to use this medication, as it contains important information for you.
- Keep this prospect, as you may need to read it again.
- If you have any doubts, consult your doctor or pharmacist.
- This medication has been prescribedonlyto you and should not be given to other people even if they have the same symptomsas you, as it may harm them.
- Ifyou experienceadverse effects,consult your doctor or pharmacist,even if they are adverse effects not listed in this prospect, See section 4.
1. What isTobrabactand for what it is used
2. What you need to knowbeforestarting touse Tobrabact
3. How to use Tobrabact
4. Possible adverse effects
5. Storage ofTobrabact
6. Contents of the package andadditional information
Tobramycin belongs to a group of medicines called aminoglycoside antibiotics.
Tobrabact is used as a local treatment for eye infections such as: conjunctivitis, keratitis, and corneal ulcers caused by bacteria sensitive to tobramycin.
Antibiotics are used to treat bacterial infections and do not work for viral infections, such as the flu or a cold. It is essential to follow the instructions regarding the dose, administration interval, and treatment duration indicated by your doctor. Do not save or reuse this medication. If you have any leftover antibiotic after treatment, return it to the pharmacy for proper disposal. Do not dispose of medications through the drain or in the trash. |
Do not use Tobrabact:
Warnings and precautions
Consult your doctor before using Tobrabact.
If you have any questions, do not hesitate to contact your doctor or pharmacist.
Children and adolescents
Tobrabact can be administered to children from one year of age at the same dose as in adults.
Other medications and Tobrabact
Inform your doctor or pharmacist if you are using, have used recently, or may need to use any other medication.
Foods and beverages
Not applicable
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor or pharmacist before using Tobrabact. Only they can adapt the treatment to suit your condition.
Do not use Tobrabact during pregnancy due to the identified risks associated with taking this medication (oral and injectable).
Do not use Tobrabact during breastfeeding.
Exercise
Not applicable.
Driving and operating machinery
If you experience temporary blurred vision after using Tobrabact, do not drive or operate machinery until your vision clears.
Tobrabact contains benzalkonium chloride
This medication contains 2.8 micrograms of benzalkonium chloride in each drop equivalent to 0.1 mg/ml.
Benzalkonium chloride can be absorbed by soft contact lenses and may alter the color of contact lenses. Remove contact lenses before using this medication and wait 15 minutes before reinserting them.
Benzalkonium chloride may cause eye irritation, especially if you have dry eye or other corneal diseases (transparent layer at the front of the eye). Consult your doctor if you feel a strange sensation, stinging, or pain in your eye after using this medication.
Follow the administration instructions exactly as indicated by your doctor or pharmacist.forTobrabact. If in doubt, consult your doctor or pharmacist again.
Use in children and adolescents
The recommended dose for adults and children over 1 year is one drop instilled in the affected eye or eyes three to eight times a day. In the case of a more serious infection, one drop may be applied to the affected eye or eyes until improvement is noted. Then, gradually reduce the dose.
Treatment duration: 5 to 15 days.
No dose adjustment is necessary for children over 1 year of age or elderly patients.
Usage instructions:
Ifyou use moreTobrabactthan you should
It is unlikely that you will experience any clinical effects. Do not apply additional drops until it is time to administer the next dose.
If you forgot to use Tobrabact
Apply the drops as soon as you remember. However, if it is almost time for the next administration, do not double the dose. Continue with the regular dosing schedule.
Like all medications, Tobrabact can produce adverse effects, although not all people may experience them.
With Tobrabact the following adverse effects have been observed:
Reporting Adverse Effects:
If you experience any type of adverse effect, consult your doctor, pharmacist, or nurse, even if it is a possible adverse effect not listed in this prospectus. You can also report them directly through the Spanish System for Pharmacovigilance of Medicines for Human Use wwww.notificaRAM.es
By reporting adverse effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
Expiration Date
Do not use this medication after the expiration date that appears on the bottle. The expiration date is the last day of the month indicated.
Storage Conditions
Store below 25 °C. Do not freeze.
Close the bottle immediately after each use.
Dispose of the bottle 15 days after opening, even if solution remains.
Do not use after the expiration date that appears on the bottle and its packaging.
Medications should not be disposed of through drains or trash. Deposit containers and medications you no longer need at the SIGRE collection point at the pharmacy. Ask your pharmacist how to dispose of containers and medications you no longer need. By doing so, you will help protect the environment.
Composition of Tobrabact
• The active ingredient is tobramycin (3 mg/ml).
The other components are benzalkonium chloride, boric acid, anhydrous sodium sulfate, sodium chloride, tiloxapol, and water for injections.
Appearance of Tobrabact and contents of the packaging
Tobrabact is a sterile, preserved, and isotonic aqueous solution administered in the form of eye drops.
Tobrabact is available in a 5 ml bottle.
Marketing Authorization Holder
MEDICOM HEALTHCARE IRELAND LIMITED
Joyce House
21-23 Holles Street
Dublin 2
Ireland
Responsible Manufacturer of the Batch:
EXCELVISION.
Rue de la Lombardière 07100 Annonay,
France.
Local Representative:
Bausch & Lomb S.A.
Avda. Valdelaparra 4. 28108
Alcobendas (Madrid)
Spain
This leaflet was last approved on: 04/2022
The detailed information of this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es//
Have questions about this medication or your symptoms? Connect with a licensed doctor for guidance and personalized care.