Table 4 |
||||||||
|
Analysis of arthritis patients according to gastrointestinal adverse events |
||||||||
|
Number of |
Incidence of events (%) |
|||||||
|
|
||||||||
|
Outcome and comparisons |
Celecoxib daily dose |
Comparator and daily dose |
Trials |
Patients |
Celecoxib |
Comparator |
Relative riska (95% CI) |
NNTpb or NNHc (95% CI) |
|
|
||||||||
|
Patient with any adverse event |
||||||||
|
|
||||||||
|
Celecoxib v placebo |
Any |
Placebo |
19 |
9,919 |
55 |
48 |
1.08 (1.04–1.13)a |
15 (11–21)c |
|
Celecoxib v paracetamol |
Any |
Paracetamol 4,000 mg |
2 |
1,056 |
32 |
32 |
1.0 (0.84–1.2) |
|
|
Celecoxib v rofecoxib |
Any |
Rofecoxib 25 mg |
3 |
769 |
48 |
49 |
0.97 (0.84–1.1) |
|
|
Celecoxib (200/400) v NSAID |
200–400 mg |
NSAID to maximum daily |
19 |
22,615 |
45 |
50 |
0.92 (0.89–0.95)a |
18 (14–23)b |
|
Celecoxib (any dose) v NSAID |
Any |
NSAID to maximum daily |
20 |
31,711 |
53 |
60 |
0.96 (0.94–0.98)a |
15 (13–18)b |
|
Celecoxib (any dose) v any active |
Any |
Any active comparator |
24 |
33,400 |
53 |
59 |
0.96 (0.94–0.98)a |
17 (14–21)b |
|
|
||||||||
|
Patient with any treatment-related adverse event |
||||||||
|
|
||||||||
|
Celecoxib v placebo |
Any |
Placebo |
19 |
9,919 |
9.5 |
8.1 |
1.22 (1.06–1.40)a |
71 (39–450)c |
|
Celecoxib v paracetamol |
Any |
Paracetamol 4,000 mg |
3 |
1,056 |
9.0 |
8.8 |
1.04 (0.71–1.5) |
|
|
Celecoxib v rofecoxib |
Any |
Rofecoxib 25 mg |
4 |
1,579 |
6.6 |
9.0 |
0.74 (0.53–1.04) |
|
|
Celecoxib (200/400) v NSAID |
200–400 mg |
NSAID to maximum daily |
19 |
22,615 |
13.0 |
17.3 |
0.77 (0.72–0.82)a |
24 (19–31)b |
|
Celecoxib (any dose) v NSAID |
Any |
NSAID to maximum daily |
19 |
23,743 |
12.7 |
17.3 |
0.77 (0.72–0.82)a |
22 (18–27)b |
|
Celecoxib (any dose) v any active |
Any |
Any active comparator |
24 |
26,242 |
12.3 |
16.2 |
0.78 (0.73–0.83)a |
26 (21–33)b |
|
|
||||||||
|
Patient with any serious adverse event |
||||||||
|
|
||||||||
|
Celecoxib v placebo |
Any |
Placebo |
19 |
9,919 |
1.0 |
1.4 |
0.67 (0.46–0.98)a |
280 (120–790)b |
|
Celecoxib v paracetamol |
Any |
Paracetamol 4,000 mg |
2 |
1,056 |
0.5 |
0.6 |
0.76 (0.14–4.1) |
|
|
Celecoxib v rofecoxib |
Any |
Rofecoxib 25 mg |
5 |
2,671 |
2.3 |
2.1 |
1.1 (0.68–1.9) |
|
|
Celecoxib (200/400) v NSAID |
200–400 mg |
NSAID to maximum daily |
19 |
22,612 |
2.5 |
2.6 |
0.91 (0.77–1.08) |
|
|
Celecoxib (any dose) v NSAID |
Any |
NSAID to maximum daily |
20 |
31,708 |
3.3 |
3.6 |
1.02 (0.91–1.15) |
|
|
Celecoxib (any dose) v any active |
Any |
Any active comparator |
26 |
35,299 |
3.2 |
3.4 |
1.02 (0.91–1.15) |
|
|
|
||||||||
|
Patient with any gastrointestinal adverse event |
||||||||
|
|
||||||||
|
Celecoxib v placebo |
Any |
Placebo |
17 |
9,512 |
26.0 |
19.0 |
1.2 (1.1–1.4)a |
14 (12–19)c |
|
Celecoxib v paracetamol |
Any |
Paracetamol 4,000 mg |
2 |
1,056 |
12.0 |
11.0 |
1.1 (0.8–1.6) |
|
|
Celecoxib v rofecoxib |
Any |
Rofecoxib 25 mg |
5 |
2,671 |
16.0 |
18.0 |
0.87 (0.74–1.03) |
|
|
Celecoxib (200/400) v NSAID |
200–400 mg |
NSAID to maximum daily |
18 |
30,043 |
26.0 |
34.0 |
0.84 (0.81–0.87)a |
12 (10–13)b |
|
Celecoxib (any dose) v NSAID |
Any |
NSAID to maximum daily |
18 |
31,171 |
26.0 |
34.0 |
0.84 (0.81–0.87)a |
12 (10–13)b |
|
Celecoxib (any dose) v any active |
Any |
Any active comparator |
24 |
34,762 |
26.0 |
32.0 |
0.85 (0.82–0.88)a |
14 (12–16)b |
|
|
||||||||
|
aRelative risk: bold indicates statistically significant difference. bNNTp (number-needed-to-treat to prevent one event) is indicated by bold. cNNH (number-needed-to-treat to harm one patient). CI, confidence interval; NSAID, nonsteroidal anti-inflammatory drug. |
||||||||
|
Moore et al. Arthritis Research & Therapy 2005 7:R644 doi:10.1186/ar1704 |
||||||||