Table 2 |
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|
Adverse Events in ≥ 20% of Study Population |
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|
Adverse Event, n (%) |
MF-DPI 200 μg QD AM (n = 78) |
MF-DPI 100 μg BID (n = 74) |
BDP 168 μg BID (n = 81) |
|
|
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|
Allergy |
22 (28) |
11 (15) |
20 (25) |
|
Fever |
18 (23) |
20 (27) |
26 (32) |
|
Headache |
33 (42) |
27 (36) |
25 (31) |
|
Viral infection |
27 (35) |
26 (35) |
29 (36) |
|
Nasal congestion |
7 (9) |
17 (23) |
11 (14) |
|
Pharyngitis |
26 (33) |
25 (34) |
25 (31) |
|
Rhinitis |
29 (37) |
20 (27) |
22 (27) |
|
Sinusitis |
15 (19) |
15 (20) |
11 (14) |
|
Upper respiratory tract infection |
38 (49) |
35 (47) |
41 (51) |
|
|
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|
BID = twice daily; BDP = beclomethasone dipropionate; MF-DPI = mometasone furoate administered via a dry powder inhaler; QD AM = once daily in the morning. |
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|
Noonan et al. BMC Pediatrics 2009 9:43 doi:10.1186/1471-2431-9-43 |
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