Oslif Breezhaler

indacaterol

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This is a summary of the European public assessment report (EPAR) for Oslif Breezhaler. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Oslif Breezhaler.

What is Oslif Breezhaler?

Oslif Breezhaler is a medicine that contains the active substance indacaterol. It is available as capsules containing a powder for inhalation (150 and 300 micrograms).

What is Oslif Breezhaler used for?

Oslif Breezhaler is used to keep the airways open in adults with chronic obstructive pulmonary disease (COPD). COPD is a long-term disease in which the airways and air sacs inside the lungs become damaged or blocked, leading to difficulty breathing air in and out of the lungs.

The medicine can only be obtained with a prescription.

How is Oslif Breezhaler used?

Oslif Breezhaler capsules are only used with a Oslif Breezhaler inhaler and must not be swallowed. To take a dose, the patient places a capsule into the inhaler and breathes the powder in through the mouth.

The recommended dose is one 150-microgram capsule, once a day at the same time each day. A dose of one 300-microgram capsule may be used in cases of severe COPD, but this must only be done on the doctor’s instructions.

How does Oslif Breezhaler work?

The active substance in Oslif Breezhaler, indacaterol, is a beta-2-adrenergic-receptor agonist. It works by attaching to beta-2 receptors that are found in the muscle cells of many organs and that cause the muscles to relax. When Oslif Breezhaler is inhaled, indacaterol reaches the receptors in the airways and activates them. This causes the muscles of the airways to relax, helping to keep the airways open and allowing the patient to breathe more easily.

How has Oslif Breezhaler been studied?

In three main studies involving over 4,000 patients with COPD, Oslif Breezhaler at different doses has been compared with placebo (a dummy treatment), tiotropium or formoterol (other inhaled medicines used to treat COPD). The main measure of effectiveness was how Oslif Breezhaler compared with placebo in improving patients’ forced expiratory volumes (FEV1) after 12 weeks. FEV1 is the most air a person can breathe out in one second.

What benefit has Oslif Breezhaler shown during the studies?

Oslif Breezhaler was more effective than placebo at improving how well the lungs work in patients with COPD. On average, the improvement in FEV1 in patients who received Oslif Breezhaler was between 150 to 190 ml, while for patients who received placebo the change in FEV1 ranged from a decrease of 10 ml to an increase of 20 ml. Overall, the effects of the 150- and 300-microgram doses of Oslif Breezhaler were similar, but the results showed that the 300-microgram dose may provide better relief in patients with more severe disease.

What is the risk associated with Oslif Breezhaler?

The most common side effects with Oslif Breezhaler (seen in between 1 and 10 patients in 100) are nasopharyngitis (inflammation of the nose and throat), upper-respiratory-tract infection (colds), sinusitis (inflammation of the sinuses), dizziness, headache, chest pain, cough, oropharyngeal (mouth and throat) pain including throat irritation, rhinorrhoea (runny nose), muscle spasm (cramps) and peripheral oedema (swelling, especially of the ankles and feet). For the full list of all side effects reported with Oslif Breezhaler, see the package leaflet.

Oslif Breezhaler must not be used in people who are hypersensitive (allergic) to indacaterol, lactose or any of the other ingredients.

Why has Oslif Breezhaler been approved?

The CHMP decided that Oslif Breezhaler’s benefits are greater than its risks and recommended that Oslif Breezhaler be given marketing authorisation.

What measures are being taken to ensure the safe use of Oslif Breezhaler?

The company that makes Oslif Breezhaler will ensure that doctors who are expected to prescribe the medicine and pharmacists in all Member States are provided with a card containing information on how the medicine is used.

Other information about Oslif Breezhaler:

European Commission granted a marketing authorisation valid throughout the European Union for Oslif Breezhaler on 30 November 2009.

For more information about treatment with Oslif Breezhaler, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist.

Name Language First published Last updated
Oslif Breezhaler : EPAR - Summary for the public BG = bălgarski 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public ES = español 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public CS = čeština 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public DA = dansk 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public DE = Deutsch 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public ET = eesti keel 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public EL = elliniká 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public EN = English 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public FR = français 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public IT = italiano 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public LV = latviešu valoda 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public LT = lietuvių kalba 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public HU = magyar 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public MT = Malti 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public NL = Nederlands 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public PL = polski 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public PT = português 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public RO = română 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public SK = slovenčina 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public SL = slovenščina 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public FI = suomi 05/01/2010 30/08/2012
Oslif Breezhaler : EPAR - Summary for the public SV = svenska 05/01/2010 30/08/2012

This EPAR was last updated on 08/04/2014 .

Authorisation details

Product details

Product details for Oslif Breezhaler
NameOslif Breezhaler
Agency product numberEMEA/H/C/001210
Active substance

indacaterol maleate

International non-proprietary name (INN) or common name

indacaterol

Therapeutic area Pulmonary Disease, Chronic Obstructive
Anatomical therapeutic chemical (ATC) code R03AC18

Publication details

Publication details for Oslif Breezhaler
Marketing-authorisation holder

Novartis Europharm Ltd.
 

Revision7
Date of issue of marketing authorisation valid throughout the European Union30/11/2009

Contact address:

Novartis Europharm Ltd.
Wimblehurst Road
Horsham
West Sussex
RH12 5AB
United Kingdom

Product information

Product information

21/11/2013  Oslif Breezhaler -EMEA/H/C/001210 -WS/0455

Name Language First published Last updated
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014
Oslif Breezhaler : EPAR - Product Information SV = svenska 05/01/2010 08/04/2014

Contents

  • Annex I - Summary of product characteristics
  • Annex IIA - Manufacturing-authorisation holder responsible for batch release
  • Annex IIB - Conditions of the marketing authorisation
  • Annex IIIA - Labelling
  • Annex IIIB - Package leaflet

Please note that the size of the above document can exceed 50 pages.

You are therefore advised to be selective about which sections or pages you wish to print.


Name Language First published Last updated
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  
Oslif Breezhaler : EPAR - All Authorised presentations SV = svenska 05/01/2010  

Pharmacotherapeutic group

Drugs for obstructive airway diseases

Therapeutic indication

Oslif Breezhaler is indicated for maintenance bronchodilator treatment of airflow obstruction in adult patients with chronic obstructive pulmonary disease.

Assessment History

Changes since initial authorisation of medicine

Initial marketing-authorisation documents

Name Language First published Last updated
Oslif Breezhaler : EPAR - Public assessment report SV = svenska 05/01/2010  
Committee for medicinal products for human use, summary of positive opinion for Oslif Breezhaler SV = svenska 25/09/2009  

Authorised

This medicine is approved for use in the European Union