Make your own choices...if you wanna Pfizer Jab...go for it..
official Pfizer document that is titled Cumulative Analysis of Post-Authorization Adverse Event Records Reports, in just the first 90 days of the vaccine?s roll out under the FDA?s EUA ? from December 1st. 2020 ? February 28th, 2021 ? there were TENS OF THOUSANDS of reported adverse reactions, including OVER 1200 DEATHS.
The report only included adverse events to the vaccine that researchers considered ?serious cases,? there were thousands more submissions that were left out of this data.
Any cases deemed ?non-serious? would be processed within 90 days, but this report was released before 90 days of Pfizer?s vaccine being available had even passed.
?Due to the large numbers of spontaneous adverse event reports received for the product, the MAH has prioritised the processing of serious cases, in order to meet expedited regulatory reporting timelines and ensure these reports are available for signal detection and evaluation activity.
Non-serious cases are processed as soon as possible and no later than 90 days from receipt. Pfizer has also taken a multiple actions to help alleviate the large increase of adverse event reports.?
In all, the report states that there were a total of 42,086 case reports of individuals who had an adverse reaction to Pfizer?s vaccine worldwide, with the largest number (13,739) coming from the United States and from the UK (13,404).
According to the documents women (29,914) were over 3x more likely to experience a reaction than men (9182). A total of 1223 individuals had a fatal reaction to the experimental Pfizer vaccine.
The document also makes it clear that the data only includes ?recorded adverse events,? which even the author admits is likely just a portion of the true number of adverse reactions that took place.
Again, keep in mind, this is within the first 90 days of the Pfizer jab?s availability.
?Reports are submitted voluntarily, and the magnitude of underreporting is unknown.
Some of the factors that may influence whether an event is reported include: length of time since marketing, market share of the drug, publicity about a drug or an AE, seriousness of the reaction, regulatory actions, awareness by health professionals and consumers of adverse drug event reporting, and litigation.?
https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf