“…Of the 150 patients with asthma, during the study period, 63 were treated with inhaled fluticasone propionate (FP; Flutide; GlaxoSmithKline, Tokyo, Japan), 63 with inhaled budesonide (BUD; Pulmicort; AstraZeneca, Osaka, Japan), eight with inhaled hydrofluoroalkane beclomethasone dipropionate (BDP; Qvar; Schering-Plough, Tokyo, Japan), eight with inhaled salmeterol/ FP (Seretide; GlaxoSmithKline), six with inhaled hydrofluoroalkane ciclesonide (CIC) (Alvesco; Teijin Pharma, Tokyo, Japan) and two with inhaled chlorofluorocarbon BDP (Aldecin; Schering-Plough). The daily dose of ICS was adjusted to an equipotent dose: with the dose of chlorofluorocarbon BDP as reference, the conversion factors used to calculate equipotent doses were 1.25 for BUD and 2.0 for FP, hydrofluoroalkane BDP and hydrofluoroalkane CIC [17][18][19].…”