TABLE 3

Overall summary of adverse events (AEs)

Tiotropium Respimat 5 µg once dailyTiotropium Respimat 2.5 µg once dailyPlacebo Respimat once dailyTotal
Patients n130127135392
Patients with any AE43 (33.1)42 (33.1)48 (35.6)133 (33.9)
Patients with severe AEs3 (2.3)003 (0.8)
Patients with investigator-defined drug-related AEs001 (0.7)1 (0.3)
Patients with AEs leading to discontinuation of trial medication001 (0.7)1 (0.3)
Patients with serious AEs2 (1.5)1 (0.8)03 (0.8)
AEs in >2% patients, by preferred term#
 Asthma15 (11.5)14 (11.0)14 (10.4)43 (11.0)
 Decreased peak expiratory flow rate5 (3.8)9 (7.1)13 (9.6)27 (6.9)
 Nasopharyngitis5 (3.8)6 (4.7)4 (3.0)15 (3.8)
 Rhinitis1 (0.8)3 (2.4)3 (2.2)7 (1.8)
 Upper respiratory tract infection3 (2.3)1 (0.8)3 (2.2)7 (1.8)
 Viral infection01 (0.8)4 (3.0)5 (1.3)
 Allergic rhinitis02 (1.6)3 (2.2)5 (1.3)
 Tonsillitis3 (2.3)01 (0.7)4 (1.0)
 Viral respiratory tract infection1 (0.8)03 (2.2)4 (1.0)