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First Batch of Pfizer Vaccine Docs Turned Over and it's as Bad as We Thought


No time to read, check out the video "10K Pages of Pfizer Docs Reveal 158K Adverse Events, 42K Case Reports, 1.2K Deaths in First 3 Months"


In case you haven't been following the story, the nonprofit group Public Health and Medical Professionals for Transparency (PHMPT) filed a Freedom of Information Act (FOIA) lawsuit against the FDA in September of last year in a US District Court in Texas. They made it clear that they had formed no opinion but wanted to have the data used to approve the Pfizer Vaccine be made public so independent experts could conduct their own reviews and analysis of it. The FDA did everything they could to fight and slow roll this process, first claiming they needed 50 years and later raising it to 75 years. The judge told them that they would have the same 108 days it took them to approve the vaccine and said that starting on March 1, 2022 they would be required to turn over the first batch of documents and this would continue until all 329,000 documents had been provided.


This month they released 10,000 documents. That will be followed by 10,000 documents on April 1, then 80,000 documents on May 1, June 1, and July 1. That will be followed by 70,000 documents on August 1 and then 55,000 documents on the first of every month until December. It is highly likely that the FDA and Pfizer will do their best to hold back the most damning of the documents until the end of the year as there is no requirement as to the order in which documents have to be turned over in.


Out of the first batch of documents to be turned over, there are already some major red flags being discovered. One of the documents that is getting lots of attention is listed as “5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021” This document listed adverse reactions reported from the Pfizer Vaccine use in the three month period between December 1, 2020, and February 28, 2021, when it first came out under the Emergency Use Authorization.



During the three-month time period, here is what their data showed. There were 42,086 case reports claiming to have 158,893 adverse reaction events including a reported 1,223 deaths. That means each report had between three and four side effects. It is important to say that none of the deaths were officially verified to be as a result of the vaccine but the individuals and doctors who reported them believed they were. Most of the reports came from the United States and United Kingdom which makes sense as they got more Pfizer vaccines in those places. It should also be mentioned that the data admits that reporting was done on a voluntary basis and thus the numbers are underrepresented. Some experts believe the VAERS numbers are likely for or five times higher than what is generally reported.



Here are a couple of other numbers which stood out from the data. There were 51,335 general disorders and administration site conditions, 25,957 nervous system disorders, 17,283 Musculoskeletal and connective tissue disorders, 14,096 Gastrointestinal disorders, 8,476 skin and subcutaneous tissue disorders, 8,848 respiratory, thoracic, and mediastinal disorders, 4,610 infections and infestations, 5,590 injuries, poisoning, and procedural complications as well as 1,403 reports of Cardiovascular adverse reactions of special interest. This includes Acute myocardial infarction, Arrhythmia, Cardiac failure, Cardiac failure acute, Cardiogenic shock, Coronary artery disease, Myocardial infarction, Postural orthostatic tachycardia syndrome, Stress cardiomyopathy, and Tachycardia.


Then at the very end of the document, there is an appendix of every condition that the researchers compiled from the reports. While it can't be said with certainty that everything on the list was a result of the vaccine, it was seen in enough people to warrant adding it as a possible side effect. You might think there would be around a hundred conditions but the nine page list actually has 1,291 side effects. The document also conveniently redacts the number of doses of the vaccine that were given making it impossible to calculate the percentages that each side effect shows up in. An ,educated guess puts the number of people who got the vaccine and experienced at least one adverse reaction to be around 1 in every 1,200 people but without the actual number it is hard to know for sure. Also, keep in mind that this was the first three months that the Pfizer vaccine was available for the public. Despite the initial reports they got, the FDA went on to approve it as safe to continue distribution. As of March 4, 2022, the current VAERS numbers sit at 25,158 deaths, 138,247 hospitalizations, 122,734 trips to urgent care, 14,544 cases of Bell's Palsy, 4,279 miscarriages, 12, 953 heart attacks, 35,913 cases of myocarditis/pericarditis, 46,515 reports of permanent disability, and many more reported adverse reactions. Like the data in the document, it is believed these numbers could be three to five times higher. What is not in doubt is that this is just the first document dump from the FDA and Pfizer. There are still more than three-hundred thousand documents to be released. At the very least this data proves that they were seeing adverse reactions to the vaccines right away and this should have never been approved without a lot more research and it should have never been mandated on anyone for any reason. Written by Chris Turner Online Content Committee Chair Sources: https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf https://phmpt.org/pfizers-documents/ https://openvaers.com/covid-data https://www.youtube.com/watch?v=NxIrp-Kp81E