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. 2002 May 22;3:10. doi: 10.1186/1471-2296-3-10

Table 3.

Summary of safety data

Placebo Etoricoxib 90 mg Naproxen 1000 mg
(N = 357) (N = 353) (N = 181)
n (%) n (%) n (%)
Number of patients:
 With any drug-related clinical adverse event 55 (15.4) 82 (23.2) 35 (19.3)
 With any serious clinical adverse event 3 (0.8) 7 (2.0) 3 (1.7)
 Discontinued due to clinical adverse event 6 (1.7) 9 (2.5) 5 (2.8)

p < 0.05 vs placebo. 

Serious adverse events were: placebo (3 patients) – thrombophlebitis, atrial fibrillation, and pneumothorax; etoricoxib (7 patients) – pulmonary embolism, angina pectoris, thyroid cancer, duodenal ulcer, hip pain, femoral fracture, and traumatic arthropathy plus corneal degeneration (in the same patient); naproxen (3 patients) – hypertension, intervertebral disc displacement, and retinal detachment.