Last July, FDA’s examination of the Medicare database revealed an excess of heart attacks, pulmonary emboli, and two bleeding disorders post Pfizer vaccination.
An AEI is an adverse event of special interest, in other words, one that FDA has already determined it should be seeking. Here is what the FDA posted about it: … near real-time surveillance detected four potential AEIs in the Medicare healthcare claims database of persons aged 65 years and older who had received the…