An observational evaluation of prescribing of fixed-dose combination inhaled corticosteroid / long-acting beta2-agonist (ICS/LABA): fluticasone propionate / formoterol (FP/FOR) and adverse events in routine primary care at 18-months and 36-months post launch

08/02/2016
23/04/2024
EU PAS number:
EUPAS12330
Study
Finalised
Documents
Study protocol
Study results
Study results
English (6.22 MB - PDF) View document
English (5.12 MB - PDF) View document
Study report
Other information