I will use that to
come to this whole issue of data, and I will a
pproach it from two points of view: First, the general issue that we've been dealing throughout all of our studies, which deals with the clinical trial process through to the post-approval monitoring, through to, as you have very effectively pointed out, in addition to all that we have learned, the absence of good data collection in all levels o
f drug interactions across ...[+++] the country — and I'm talking broadly — even though there are clear examples of how effectively it can be done, and the importance of that; then I want to come to the Vioxx issue as a specific example of the complexity of the issue of benefit and harm.