The FDA/Pfizer FOIA request initial reading
So, the FDA began to produce the documents used to approve the Pfizer vaccination (following the infamous Freedom of Information Act request). I have not had a chance to go through them thoroughly yet… but here is a quick summary of the Post-Authorization Adverse Event Report.
This report runs up until February 28, 2021. In other words, this is only an early glimpse of the AE information in the FDA's possession. Over 60% of these Ads were confirmed by medical professionals. In other words, so much for the “reports can be submitted by anyone” narrative.
Many of these were SAEs:
Below is a quick summary of the fatal incidents as listed in the document:
Anaphylaxis 9
Autoimmune 12
Cardiovascular 136
COVID-19 136
Haematological 34
Hepatic 5
Medication Error 7
Neurological 16
Other 96
Renal 23
Respiratory Failures / Related 41
Stroke 61
Thromboembelic Events 18
Vaccine Associated Enhanced Disease 38
Vaccine Effectiveness 65
Vasculitic 1
Total: 698
Note, this does not add up to 1223 reported earlier in the document. I may have missed the explanation? My speculation is that the inclusive criteria required either deaths to be reported by medical professionals, or the causes were unknown for the remainder.
In any case, it is funny to see that regardless of the injuries listed, no signals were triggered. Is this because the FDA already knew the vaccine caused these types of injuries? That would be strange considering how long it took them to make announcements on harmful As a (the linked announcement stood out to me as I have a friend that took the vaccine two days before said announcement. He was then diagnosed with myocarditis by his doctor the day after the announcement).
Or perhaps they had no interest in investigating safety signals at all. I do not think there was a terminal condition for these vaccines, so I am inclined to think that it was the latter.
In any case, as I noted, I am short on time and it is hard to glean useful information from a document of this nature. But I suspect the FDA is going to be extremely embarassed sometime in the next 55 years.
