This is a retrospective, multicentre, non-interventional, observational study in patients with asthma and/or COPD who are treated with budesonide-formoterol.
In July 2018 Norwegian authorities decided to allow switch at pharmacy for dry powder inhalers (DPIs) containing budesonide-formoterol. Pharmacists are instructed to switch patients to the inhaler with the lowest price. The pharmacist will train the patient on how to use the new inhaler. All patients whose eligible inhaler switch occurred between 1st July 2018 and 1st March 2019 will be eligible for the study.
Study Type
OBSERVATIONAL
Enrollment
29
Dry powder inhaler
Flattum Legesenter
Hønefoss, Norway
Disease control
The number of asthma and/or COPD exacerbations during the 12 months pre-switch and the 12 months post-switch.
Time frame: 24 months
Budesonide-formoterol dose
The change in the treatment dose of budesonide-formoterol at the time of the eligible switch and at the end of the post-switch period (e.g. 12 months post-switch).
Time frame: 24 months
Training at pharmacy
The correlation between inhaler training given at pharmacy and exacerbations.
Time frame: 24 months
Healthcare utilisation
The number of asthma and/or COPD related hospitalisations, emergency room visits and visits to physicians 12 months pre-switch and 12 months post-switch.
Time frame: 24 months
Inhaler switch
The number of re-switches after the first 'eligible' switch and the reasons for that switch.
Time frame: 24 months
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