Table 3 |
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|
GI end points |
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|
Celecoxib (n = 28,614) |
nsNSAID (n = 15,278) |
Placebo (n = 5,827) |
Rofecoxib (n = 1,329) |
Total (n = 51,048) |
|
|
|
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|
CSULGIEs, n (%) |
37 (0.1) |
40 (0.3) |
12 (0.2) |
0 (0) |
89 (0.2) |
|
|
|||||
|
Incidence ratea |
0.3 |
0.9 |
0.3 |
0 |
0.4 |
|
|
|||||
|
CSULGIEs or symptomatic ulcers, n (%) |
47 (0.2) |
44 (0.3) |
12 (0.2) |
0 (0) |
103 (0.2) |
|
|
|||||
|
Incidence ratea |
0.4 |
1.0 |
0.3 |
0 |
0.5 |
|
|
|||||
|
CSULGIEs, symptomatic ulcers, or hemoglobin decrease, n (%) |
281 (1.0) |
343 (2.3) |
52 (0.9) |
4 (0.3) |
680 (1.3) |
|
|
|||||
|
Incidence ratea |
2.3 |
7.4 |
1.4 |
2.6 |
3.3 |
|
|
|||||
|
aIncidence rate based on 100 patient-years of exposure to drug. CSULGIEs, clinically significant upper and lower GI events; nsNSAID, nonselective nonsteroidal antiinflammatory drug. |
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|
Moore et al. Arthritis Research & Therapy 2013 15:R6 doi:10.1186/ar4134 |
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