


Ask a doctor about a prescription for COLFINAIR 2 MILLION IU POWDER FOR SOLUTION FOR NEBULIZER INHALATION
Package Leaflet: Information for the User
Colfinair 2 million UIpowder for solution for inhalation by nebulizer
colistimethate sodium
Read all of this leaflet carefully before you start using this medicine, because it contains important information for you.
Contents of the package leaflet:
Antibiotics are used to treat bacterial infections and are not effective against viral infections. It is essential that you follow the instructions regarding dosage, administration interval, and treatment duration as indicated by your doctor. Do not store or reuse this medication. If you have any leftover antibiotic after completing treatment, return it to the pharmacy for proper disposal. Do not dispose of medications through the drain or in the trash. |
Colfinair is administered by inhalation to treat chronic respiratory infections in patients with cystic fibrosis. Colfinair is used when these infections are caused by a specific bacterium called Pseudomonas aeruginosa.
Do not use Colfinair
Warnings and precautions
Consult your doctor, pharmacist, or nurse before starting to use Colfinair:
In premature infants and newborns, caution should be exercised when using Colfinair because the kidneys are not yet fully developed.
Coughing and chest tightness may lead to interruption. This can be alleviated with the use of an inhaled bronchodilator (e.g., salbutamol) before using Colfinair. Your doctor will supervise your first dose of Colfinair and check your lung function before and after administration.
If, despite using a bronchodilator, you experience chest tightness, inform your doctor because this may indicate an allergic reaction and treatment should be discontinued.
During treatment with Colfinair, neurotoxicity may occur with possible dizziness, confusion, or visual disturbances. If you experience side effects such as dizziness, confusion, or visual disturbances, or any not mentioned in this leaflet, inform your doctor.
Taking Colfinair with other medicines
If you have myasthenia gravis and are also taking other antibiotics called macrolides (such as azithromycin, clarithromycin, or erythromycin), or antibiotics called fluoroquinolones (such as ofloxacin, norfloxacin, and ciprofloxacin), taking Colfinair increases the risk of muscle weakness and respiratory difficulties even more.
Receiving colistimethate sodium by infusion at the same time as receiving Colfinair by inhalation may increase your risk of experiencing side effects.
Colfinair must not be mixed with any other medicine in the nebulizer!
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medicine.
Driving and using machines
Colfinair has a moderate influence on the ability to drive and use machines. During treatment with Colfinair, neurotoxicity may occur with possible dizziness, confusion, or visual disturbances. If you experience any side effects such as dizziness, confusion, or visual disturbances, do not drive or use machines and consult your doctor or pharmacist.
Colfinair is for inhalation use only.
Follow the instructions for administration of this medicine exactly as indicated by your doctor. If in doubt, consult your doctor or pharmacist again.
The recommended dose is:
Proposed dose | Maximum daily dose | |
Adults, Adolescents (12 to 17 years), Children (2 to 11 years) | 1-2 million units two or three times a day | 6 million units |
Children under 2 years | 0.5-1 million units, twice a day | 2 million units |
Your doctor may decide to adjust the dose depending on your circumstances. If you are also taking other inhaled medicines, your doctor will tell you in what order to take them.
Note that Colfinair is also available in a vial of 1 million UI, which may be a more suitable dose depending on the dosage prescribed by your doctor.
For use in children under 2 years of age, PARI LC SPRINT Baby (red nozzle adapter) with a mask is recommended.
Your doctor will tell you how long your treatment with Colfinair will last. Do not stop treatment early because when treating bacterial infections, it is essential to complete the full course of treatment to reduce the risk of developing resistance to the infectious bacteria.
Preparation for inhalation treatment
If you are being treated at home, your doctor or nurse will show you how to use Colfinair in your nebulizer when you start this treatment.
To start your treatment, you will need the following:
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How to prepare Colfinair for inhalation
Before you can introduce Colfinair into the nebulizer and inhale it, it must be dissolved with 3 ml of sterile NaCl 0.9% solution for inhalation. An ampoule contains the correct volume to dissolve Colfinair.
Colfinair must be used immediately after dissolution. Do not dissolve Colfinair until you are ready to administer a dose (see also section 5).
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Step 5
Use Colfinair only when all the powder has dissolved and there are no visible particles in the solution
How to use Colfinair
Colfinair is for inhalation use only with a suitable nebulizer (e.g., eFlowrapidor PARI LC SPRINT).
Read the nebulizer's instructions for use carefully to obtain more information about handling the nebulization system.
It is essential that your nebulization system functions correctly before starting treatment with Colfinair.
Place the components of your nebulizer on a flat, clean surface and follow the manufacturer's instructions for use.
Inhalation should be done in a well-ventilated room.
After inhaling Colfinair
Consult the manufacturer's instructions for use of the nebulizer for cleaning and disinfecting it.
If you use more Colfinair than you should
If you have used more Colfinair than you should, consult your doctor or pharmacist immediately. If too much Colfinair is administered accidentally, the effects can be severe and may include kidney problems, muscle weakness, and respiratory difficulty (even arrest).
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately, or call the Toxicology Information Service, phone 915 620 420 (indicating the medication and the amount ingested), or go to the nearest hospital.
If you forget to use Colfinair
If you are treating yourself and have forgotten a dose, you should take the forgotten dose as soon as you remember and then the next dose 8 or 12 hours later, and continue from then on as instructed.
Do not take a double dose to make up for forgotten doses.
If you stop using Colfinair
You must not stop using Colfinair as prescribed without consulting your doctor first.
If you have any other questions about the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
An allergic reaction may occur. Severe allergic reactions can occur even with the first dose and may include rapid onset of rash, swelling of the face, tongue, and throat, inability to breathe due to narrowing of the airways, and loss of consciousness. Urgent medical attention will be needed.
If you think you have an allergic reaction to Colfinair, inform your doctor immediately.
Some side effects can be serious
Very common: may affect more than 1 in 10 people.
Frequency not known: cannot be estimated from the available data.
If you experience any of these effects, inform your doctor immediately.
Other possible side effects
Very common: may affect more than 1 in 10 people.
If any of these problems affect you severely, inform your doctor.
Frequency not known: cannot be estimated from the available data.
Other possible side effects include thrush in the mouth or throat.
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly through the Spanish Medicines and Healthcare Products Agency (AEMPS) https://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 this medicine after the expiry date which is stated on the carton or vial label after EXP. The expiry date is the last day of the month indicated.
Do not store above 25°C.
Keep the vial in the outer carton to protect it from light.
Colfinair solution for inhalation by nebulizer should be used immediately after preparation. If this is not possible, a Colfinair solution should be stored in the refrigerator (2°C - 8°C) and not more than 24 hours.
If not used immediately, storage conditions and times are the responsibility of the user.
Any leftover solution should be discarded.
For single use only.
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.
Composition of Colfinair
Appearance and packaging of the product
Colfinair is a powder for solution for inhalation by nebulizer.
2 million UI/vial: | White powder in a 10 ml colorless glass vial with a lavender cap. |
Also available: 1 million UI/vial: | White powder in a 10 ml colorless glass vial with a red cap. |
The product is available in the following pack sizes:
Carton box containing:
Marketing authorization holder and manufacturer
PARI Pharma GmbH
Moosstrasse 3
82319 Starnberg
Germany
Tel.: +49 (0) 89/74 28 46 – 10
You can request more information about this medicine by contacting the local representative of the marketing authorization holder:
PARI Pharma Iberia S.L.
Miguel Yuste 17, 4th floor C.
28037 Madrid
This medicine is authorized in the Member States of the European Economic Area under the following names:
GermanyColiFin 2 Millionen. I.E. Pulver zur Herstellung einer Lösung für einen Vernebler
NetherlandsColiFin PARI 2.000.000 IE Poeder voor verneveloplossing
AustriaColiFin 2 Mio. I. E. Pulver zur Herstellung einer Lösung für einen Vernebler
SpainColfinair 2 million UI powder for solution for inhalation by nebulizer
ItalyColfinair 2.000.000 U Polvere per soluzione per nebulizzatore
Date of last revision of this leaflet: 05/2022
Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Healthcare Products (AEMPS) http://www.aemps.gob.es/
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