FDA's nationally representative early warning system study NOW shows (after we have been screaming at FDA about these harms) that four outcomes met threshold for statistical signal following Pfizer
by Paul Alexander
vaccination including pulmonary embolism (PE; RR = 1.54), acute myocardial infarction (AMI; RR = 1.42), disseminated intravascular coagulation (DIC; RR = 1.91), immune thrombocytopenia (ITP; RR=1.44).
SOURCE:
https://www.sciencedirect.com/science/article/pii/S0264410X22014931
‘evaluated 14 outcomes of interest following COVID-19 vaccination using the US Centers for Medicare & Medicaid Services (CMS) data covering 30,712,101 elderly persons. The CMS data from December 11, 2020 through Jan 15, 2022 included 17,411,342 COVID-19 vaccinees who received a total of 34,639,937 doses.
‘early warning system is the first to identify temporal associations for PE, AMI, DIC, and ITP following BNT162b2 vaccination in the elderly.’
This ridiculous statement is made by FDA despite these findings:
‘FDA strongly believes the potential benefits of COVID-19 vaccination outweigh the potential risks of COVID-19 infection.’
https://yournews.com/2022/12/18/2476160/fda-admits-pfizers-covid-19-vaccine-linked-to-blood-clotting/
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