Going back to the real world and data integrity, a doctor in an institution or in the community prescribes a drug, an adverse reaction occurs, he or she is obligated to report it. What incentive is there for the doctor to report it? I can think of a lot of disincentives, not the least of which could be possibly legal issues or paperwork or just not accepting that there was an adverse reaction. How do you deal with those types of situations or how do you account for those types of situations when you're examining data?
I guess that goes to CIHI.