An FDA Advisory Committee convened in February, 2005 to review primarily the three selective COX-2 inhibitors available in the U.S. It concluded overwhelmingly (32 votes to zero) that these agents increase the risk of thrombotic cardiovascular events1. The evidence from several placebo-controlled clinical trials was considered conclusive. The problem was interpreted as a class effect, although the degree of harm appeared to differ among the agents. The Advisory Committee recommended that celecoxib remain on the market with major restrictions applied to its use1.

EMEA was in agreement with the FDA and recommended suspension of valdecoxib2. It also added new contraindications and warnings to the other marketed coxibs. Contraindications were added for patients with established ischemic vascular disease and reinforced warnings were issued for patients with risk factors of heart disease. Based on the same available scientific evidence, the FDA did not follow the recommendations by its Advisory Committee3. Rather the FDA added only a Black Box warning vaguely stating that celecoxib "may (author's emphasis) cause an increased risk of serious cardiovascular events,..." and that "Patients with cardiovascular disease or risk factors for cardiovascular disease may (author's emphasis) be at greater risk"4.

The recommendations for the non-selective NSAIDs by FDA and EMEA issued in 2006 also went in a different direction. EMEA concluded that the risk-benefit balance for eleven of these agents remains favorable5. However, it could not exclude "a small increase in risk of thrombotic events." FDA added to the Black Box warning for celecoxib that "All NSAIDs may (author's emphasis) have a similar risk. This risk may (author's emphasis) increase with duration of use"4. Again, the different conclusions by the regulatory agencies were based on the same available scientific evidence.

So what is the evidence for cardiotoxic effects of non-selective NSAIDs? The safety information is limited, with no large, long-term, placebo-controlled trials. In their meta-analysis, Kearney et al.6 reported summary rate ratios for high doses of naproxen, ibuprofen and diclofenac in comparison with placebo; these ratios were 0.92 (95% CI 0.67 to1.26), 1.51 (0.96 to 2.37) and 1.63 (1.12 to 2.37), respectively. The authors concluded "Our results indicated that high-dose ibuprofen (800 mg three times daily) and high-dose diclofenac (75 mg twice daily) were each associated with an increased risk of vascular events, but that the risks of high-dose naproxen (500 mg twice daily) were substantially smaller."

A recent indirect comparison supports these findings7. In 26 active-control trials comparing COX-2 inhibitors to diclofenac, the risk of vascular events was lower with the COX-2 inhibitors (relative risk 0.92; 95% CI, 0.81–1.05). For trials comparing COX-2 inhibitors to naproxen, the former were associated with an increased vascular risk (relative risk 1.57; 95% CI, 1.21 to 2.03). Thus, compared to naproxen, diclofenac may increase the vascular risk by about 70%7.

The scientific evidence points to major differences among the non-selective NSAIDs. Naproxen appears to be fairly neutral in its cardiovascular effects. In fact, at the FDA Hearing in February 2005, the Advisory Committee recommended that naproxen be the preferred NSAID comparator in future trials of painkillers1. Diclofenac has pharmacologic effects similar to those of celecoxib. The evidence is fairly overwhelming that this drug increases the risk of cardiovascular events. However, the regulatory agencies so far have not recognized these clinically important differences among the non-selective NSAIDs. Since diclofenac is the most commonly used non-selective NSAID and since it increases the risk of vascular events by 60–70%, the unrecognized harm it has caused worldwide could be enormous. Consideration ought to be given to removing this drug from the market, since there is not evidence that it offers better pain control than the large number of non-selective NSAIDs on the market.