Yes, I'll try my best. Certainly, as Dr. Godefroy mentioned, Dr. Turner would probably give you a more complete answer. We can supply things in writing as well, if you'd like.
Part of the assessment is to go beyond the report. Certainly when the marketed health products directorate looks at a spontaneous report or a case report, there are a lot of questions asked around that.
You referred to medical records and whether there were there tests done. That is all part of the assessment: what exactly was consumed, other medications or other products that may have been consumed around the same time, and the proximity of when the product might have been consumed compared with when the reaction may have occurred.
All those precise questions, in accordance with guidelines from WHO and some very specific standard operating procedures within MHPD, are done in order to complete a proper assessment.