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Table 3 Adverse events reported by more than one patient in any treatment period (treated set)

From: A randomised dose-ranging study of tiotropium Respimat® in children with symptomatic asthma despite inhaled corticosteroids

 

Patients, n (%)

 

Tiotropium Respimat ® 5 μg

Tiotropium Respimat ® 2.5 μg

Tiotropium Respimat ® 1.25 μg

Placebo Respimat ®

(n = 76)

(n = 74)

(n = 75)

(n = 76)

Patients with any adverse event

7 (9.2)

7 (9.5)

7 (9.3)

8 (10.5)

Asthma

2 (2.6)

2 (2.7)

1 (1.3)

1 (1.3)

Bronchitis

2 (2.6)

1 (1.4)

1 (1.3)

1 (1.3)

Headache

1 (1.3)

1 (1.4)

2 (2.7)

0

Nasopharyngitis

0

0

2 (2.7)

2 (2.6)

Pharyngitis

1 (1.3)

1 (1.4)

0

1 (1.3)

Rhinitis

0

2 (2.7)

0

1 (1.3)

Cough

0

0

0

2 (2.6)

Influenza

1 (1.3)

1 (1.4)

0

0

Purulence

0

0

1 (1.3)

0

Respiratory tract infection

0

0

0

1 (1.3)

Urinary tract infection

0

0

0

1 (1.3)

Viral upper respiratory tract infection

1 (1.3)

0

0

0

Stomatitis

0

0

0

1 (1.3)

Chest pain

1 (1.3)

0

0

0

Contusiona

0

0

0

1 (1.3)

Skeletal injury

0

0

0

1 (1.3)

  1. aContusion of the lower jaw. Treatment + 30 days.