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. 2014 Mar 27;14:52. doi: 10.1186/1471-2466-14-52

Table 3.

Summary of patients affected by respiratory-related adverse events

AEs classified as Respiratory, Thoracic and/or Mediastinal Disorders
 
Placebo
AZD9164
 
GMAD, healthy subjects
n = 9
400 μg
1000 μg
2800 μg
Total (%)
    n = 6 n = 6 n = 6 n = 27
Throat irritation
1 (11.1)
0 (0)
1 (16.7)
2 (33.3)
4 (14.8)
Oropharyngeal pain
0 (0)
1 (16.7)
2 (33.3)
0 (0)
3 (11.1)
Cough
0 (0)
0 (0)
0 (0)
1 (16.7)
1 (3.7)
Dyspnoea
0 (0)
0 (0)
1 (16.7)
0 (0)
1 (3.7)
JMAD, healthy subjects
n = 6
400 μg
1000 μg
 
Total (%)
 
 
n = 6
n = 6
 
n = 18
Cough
0 (0)
1 (16.7)
1 (16.7)
 
2 (11.1)
Epistaxis
0 (0)
0 (0)
1 (16.7)
 
1 (5.6)
Nasal mucosal disorder
0 (0)
0 (0)
1 (16.7)
 
1 (5.6)
Respiratory tract infection
0 (0)
0 (0)
1 (16.7)
 
1 (5.6)
Upper respiratory tract infection
0 (0)
1 (16.7)
0 (0)
 
1 (5.6)
GMAD, COPD patients
n = 1
 
n = 3
 
n = 4
Dyspnoea
1 (100)
 
2 (66.7)
 
2 (50)
Cough 0 (0)   1 (33.3)   1 (25)