Posted this on another thread too, but I think everyone is getting this wrong. This is a list "Adverse Events of Special Interest", meaning if they see any of these adverse events, then that is of interest. This is not saying these are the adverse events seen in the trial
From page 16:
The company’s AESI list takes into consideration the lists of AESIs from the following expert groups and regulatory authorities: Brighton Collaboration (SPEAC), ACCESS protocol, US CDC (preliminary list of AESI for VAERS surveillance), MHRA (unpublished guideline).
The AESI terms are incorporated into a TME list and include events of interest due to their association with severe COVID-19 and events of interest for vaccines in general.
I think what you're looking for is pg16 Table 7, that has actual numbers and what was observed. Which is still massive btw, but that page 30 is simply listing what kinds of adverse events they are interested in.
Posted this on another thread too, but I think everyone is getting this wrong. This is a list "Adverse Events of Special Interest", meaning if they see any of these adverse events, then that is of interest. This is not saying these are the adverse events seen in the trial
From page 16:
I think what you're looking for is pg16 Table 7, that has actual numbers and what was observed. Which is still massive btw, but that page 30 is simply listing what kinds of adverse events they are interested in.
Or am I the one misinterpreting this? Entirely possible since medical studies are definitely not in my wheelhouse. (link for context https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf)