Table 2: Reports submitted to Health Canada on types of suspected cardiovascular/cerebrovascular ARs associated with selective COX-2 inhibitors from date marketed to Oct. 12, 2001*
| Type of reaction | Celecoxib | Rofecoxib | Meloxicam |
|---|---|---|---|
| Increased blood pressure | 20 | 21 | 1 |
| Congestive heart failure | 7 | 17 | - |
| Myocardial infarction† | 8 | 9 | 1 |
| Angina | - | 2 | - |
| Heart rate and rhythm disorders‡ | 24 | 20 | - |
| Cerebrovascular events due to hemorrhage or cause non specified§ |
9 | 9 | - |
| Cerebrovascular events with clot | 1 | - | - |
| Thromboembolic events¶ | 8 | - | - |
| Pericardial effusion | 1 | - | - |
| Endocarditis | 1 | - | - |
| Aortic aneurysm rupture | 1 | - | - |
| Vasculitis | 3 | - | - |
*This table reports reactions, and each report may contain more than
1 reaction. These data cannot be used to determine the incidence of ARs
because neither patient exposure nor the amount of time the drug was on
the market has been taken into consideration.
†Includes myocardial ischemia.
‡Includes cardiac arrest, cardiac arrhythmia, atrial fibrillation, ventricular
fibrillation, heart block, sick sinus syndrome, tachycardia, ventricular
tachycardia, palpitation, bradycardia.
§Includes cerebrovascular accident, stroke, transient ischemic attack.
¶Includes pulmonary embolism, deep vein thrombosis, venous arm thrombosis, limb embolism,
peripheral ischemia.