"At least now we know why the FDA and Pfizer wanted to keep this data under wraps for 75 years. Start on Page 30 of the document and keep scrolling. They may have temper tantrums, bite themselves, or exhibit other behavior problems. 10,000 pages out of a cache of over 450,000 of Pfizer-BioNTech vaccine-related data, which the FDA relied upon to grant Emergency Use Authorization, can now be reviewed. Skip to content *blogg. Starting on page 30 of a newly uncovered company document, an exhaustive list of serious adverse reactions to the shot is fully outlined. The latest release of Pfizer-BioNTech COVID-19 vaccine documents raises questions about how frequently adverse events experienced by clinical trial participants were reported as "unrelated" to the vaccine. The Pfizer document was released as part of a Freedom of Information Act request by a group of more than 30 professors and scientists from universities including Harvard, Yale, Brown and UCLA. The case of Augusto Roux in Argentina suggests that in at least one . Check out the adverse events, starting at page 30. Ephesians 6:10-18. Why? According to an 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. Pittman's ruling states that the FDA must turn over 12,000 pages of documents by the end of January, then 55,000 pages every 30 days until the entirety, omitting redacted portions, of the data submitted by Pfizer has been released. noted that up to 25,957 adverse events were classified as "nervous system disorders," most of which affected women aged 30 to 51. that could be the case but often it really is due to the burden. A federal judge in Texas has ruled that the FDA must by the end of this month make public 12,000 pages of the data it used to make decisions about approvals for Pfizer/BioNTech's COVID-19 vaccine — and then release 55,000 pages every 30 days after that until all 450,000 requested pages are public. Details of the document were damning, revealing a massive number of observed adverse reactions beginning on page 30. An 80,000-page cache of Pfizer-BioNTech COVID-19 vaccine documents released by the U.S. Food and Drug Administration (FDA) sheds light on Pfizer's extensive vaccine trials in Argentina, including the unusually large size of the trials and the story of a trial participant whose vaccine reaction was "disappeared.". As mentioned, 10,000 more pages and 97 documents were released by the FDA with regards to the Pfizer trials. . Media Resources & Contact Information. These findings should put an immediate end to the Pfizer COVID . Documents with a large file size are provided in a .zip file and will need to be uncompressed after download. Pfizer will work with sites to ensure an appropriate COVID-19 prevention strategy. Pfizer releases its list of vaccine side effects. That's the side effect profile for this poisonous shot. A document from Pfizer-BioNTech entitled "5.3.6 Cumulative analysis of post-authorization adverse event reports of pf-07302048 (bnt162b2) received through 28-feb-2021" ( here) has triggered . The documents made available by PHMPT to the public are available here. Here too, the results are hair-raising and should have triggered a complete stop to the injection campaign of . The data was released by the Public Health and Medical . Leucopenia is when your body cannot fight off diseases and other types of infection. Media Inquiries; Public Health and Medical Professionals for Transparency Documents. The 80,000-page document cache released May 2 by the U.S. Food and Drug Administration (FDA) includes an extensive set of Case Report Forms (CRFs) See Page 30. The 80,000-page document cache released May 2 by the U.S. Food and Drug Administration (FDA) includes an extensive set… Internal documentation from Pfizer reveals that the company's Wuhan coronavirus (Covid-19) "vaccine" is anything but safe and effective. "This is a bombshell," said Children's Health Defense (CHD) president and general counsel Mary Holland. Arteritis;Arteritis Page 30 090177e196ea1800\Approved\Approved On: 30-A pr-2021 09:26 (GMT) FDA-CBER-2021-5683-0000083 BNT162b2 5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports . Jestre. &nbsp; The first wave of documents was released last November . 10,000 pages out of a cache of over 450,000 of Pfizer-BioNTech vaccine-related data, which the FDA relied upon to grant Emergency Use Authorization, can now be reviewed.. That list spans over eight full pages. A three present fatality rate is extremely high in terms of vaccine efficacy. . The total number of doses shipped around the world in that time period is redacted. And be sure to see the section titled "APPENDIX 1. By Michael Nevradikis, Ph.D. On page 12 of the "Cumulative Analysis of Post-Authorization Adverse Event Reports Received Through 28-Feb-2021" document, 19 you find data on pregnant and lactating women. This Is Interesting. Be sure to take a look at page 30 Ron says. Page 30. Army Flight Surgeon . many people don't understand that when these types of requests come in the requesters are not entitled to all of the data as it is. Wow. ARDS acute respiratory distress syndrome This follows U.S. District Judge Mark T. Pittman's decision . VRBPAC Briefing Document PFIZER-BIONTECH COVID-19 VACCINE (BNT162, PF-07302048) . Internal documentation from Pfizer reveals that the company's Wuhan coronavirus (Covid-19) "vaccine" is anything but safe and effective. 7 March 2022 at 11:10 AM. . September 9, 2021. In their lawsuit filed September 16, 2021, the plaintiffs asked the FDA to share the data it relied upon in licensing Pfizer's COVID-19 vaccine. Pfizer wanted to hide this until 2076 but a judge forced them to release this info. You cannot have informed consent if they hide information that assists you in making an informed consent decision. The volume of Adverse Events was so significant that pfizer made a statement to address the vaccine injuries on Pg. Documents with a large file size are provided in a .zip file and will need to be uncompressed after download. Kids, Covid, and Covid Vaccines . Printable PDF of just-released Pfizer data RenewAmerica staff March 5, 2022 Click here to see a printable PDF of the just-released Pfizer data. Pfizer's Documents. In a January court order, U.S. District Judge Mark Pittman of the Northern District of Texas required the FDA to release around 12,000 documents immediately, and then 55,000 pages a month until . March 2, 2022. Now you know why they wanted to hide it. Awakening from the trance, Pfizer smoking-gun secret document: their deadly COVID vaccine. The 80,000-page document cache released May 2 by the U.S. Food and Drug Administration (FDA) includes an extensive set of Case Report Forms (CRFs) Canada Free Press . Page 30 - APPENDIX 1. As the news cycle continues to focus on the Ukraine situation, the FDA complied with a court order to begin releasing 55,000 pages of Pfizer data per month that was used to authorize their COVID-19 vaccine produced with BioNTech, with the first batch quietly released yesterday, March 1st. 03/07/2022 / By Ethan Huff. e . The plaintiffs want the records so they can be assured, amid significant public skepticism, that the Pfizer vaccine is indeed "safe and effective." The request for FDA's Pfizer/BioNTech data flows from an August 2021 Freedom of Information . 2020 - February 28th, 2021 - there were TENS OF THOUSANDS of reported adverse reactions, including OVER 1200 DEATHS. AIDS acquired immunodeficiency syndrome . This would allow the public to have all of the FDA's information regarding Pfizer's vaccine within eight months. Start with page 30. By Michael Nevradakis, Ph.D. | The Defender | May 17, 2022 The latest release of Pfizer-BioNTech COVID-19 vaccine documents raises questions about how frequently adverse events experienced by clinical trial participants were reported as "unrelated" to the vaccine. The ones that die from the side effects are the lucky ones! The report, compiled by the "Worldwide Safety" division of Pfizer, is entitled "CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021." HERE IS THE LINK TO A PDF OF THE DOCUMENT. 1,227 deaths. PHMPT is composed of over 30 professors and scientists, who requested the federal government to share the documents that helped them decide to grant approval to Pfizer's COVID vaccine. Pfizer's Own Trial Data: 1200+ Dead, 46.5% Required Hospitalization & 30% Unrecovered in the First 2 months & 12 days of Rollout. The Facts: Documents released by the FDA in accordance with a Freedom of Information Act (FOIA) request reveal that Pfizer recorded 1,223 deaths December 1st. A court loss for the FDA in a Texas dis­trict court means the agency on Tues­day be­gan to re­lease a mas­sive trove of hun­dreds of thou­sands of doc­u­ments re­lat­ed to its re­view . It compiled data from 63 countries such as the U.S . Potential COVID-19 illness visits can be conducted via telehealth, without the need for an in-person . Among the documents the FDA was forced to release just days ago is a 38-page report titled "5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received Through 28-Feb-2021." Report Prepared by: Worldwide Safety Pfizer. But deviating sharply from the FDA's desired timeline, the judge ordered the agency to "produce the remaining documents at a rate of 55,000 pages every 30 days, with the first production being . The CDC would have been aware of some of this data via VAERS. . More videos you might like: HAARP, Morgellons, Chemtrails, Nanobots, AI, the Covid shot are interelated-The simple solution! December 30 . Fragment from: 5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021. 8. From the Pfizer data release there were 1,223 reported fatalities during 3-month period, out of 42K reported adverse events. Pfizer documents the FDA wanted sealed until 2097, were released March 1. The Gateway Pundit reports: The esteemed group of more than 30 professors and scientists asked the federal government to share any and all data that factored into the agency's hasty decision to grant Pfizer's experimental mRNA vaccine an emergency use authorization (EUA) - which amounts to a trove of over 329,000 documents.. They go from pages 30-38! Of particular interest is page 30. https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf The experts told us these covid shots are the safest in history. While the FDA initially refused, claiming it would take them 55 years to review all 329,000 pages of documents, a first batch has been released and it reportedly . COURT-ORDERED RELEASED PFIZER DOCUMENTS: The Pfizer documents that were to be sealed until 2097 were released today. New Pfizer documents! Everyone who got Jabbed has a very specific MAC ADDRESS which will be activated by 5G frequencies via Bluetooth technology! Public Health and Medical Professionals for Transparency, Pfizer / FDA FOIhttps://phmpt.orgRequest, Freedom of Information Act (FOIA) https://phmpt.org/wp-co. Dr Naomi Wolf reports regularly to Steve Bannon's War Room the revelations found in the Pfizer FOIA documents. Page 1 A PHASE 1/2/3, PLACEBO-CONTROLLED, RANDOMIZED, OBSERVER-BLIND, DOSE-FINDING STUDY TO EVALUATE THE SAFETY, TOLERABILITY, IMMUNOGENICITY, AND EFFICACY OF SARS-COV-2 RNA VACCINE CANDIDATES AGAINST COVID-19 IN HEALTHY INDIVIDUALS Study Sponsor: BioNTech Study Conducted By: Pfizer Study Intervention Number: PF-07302048 Page 1 090177e195a63925\Approved\Approved On: 30-Nov-2020 14:23 (GMT) Pfizer-BioNTech COVID-19 Vaccine VRBPAC . Of course all applicable sources are attached for corresponding literature and images. I've never seen anything like it. The potential side effects from pages 30-38 of Pfizer's data dump are: native advertising. It was not possible to determine whether these events had a causal relationship to the vaccine. The rest will be ZOMBIES ‍♂️! Starting on page 30 of the document, you will find 9 pages of adverse effects from the vaccine. AE adverse event . The FDA has made public the first batch of documents it used to authorize Pfizer's COVID shots, including a report detailing over 150,000 serious adverse events and more than 1,200 deaths . I don't think any of us are surprised by this. . They received an As a side note, just so it's clear, during the state of the union speech tonight, Biden announced masks were not longer necessary for . 39. Details of the document were damning, revealing a massive number of observed adverse reactions beginning on page 30. An FDA release of Pfizer's internal pharmacovigilance reports on vaccine adverse reactions for its novel, gene therapy Coronavirus Disease 2019 (COVID-19) vaccine reveal women who suffered significant side effects outnumbered men by a ratio of more than 3:1, and that the bulk of reactions afflicted people of both genders aged 31 to 50.. TOP SECRET PFIZER DOCUMENT LEAKS ONLINE… You can get a PDF copy of the actual document here. 6: As the title indicates, the document contains information about adverse events that occurred following vaccination, not vaccine side effects as many claimed. SS: Courts order FDA to release Pfizer's EUA data. Radiation Leukopenia is one of the Pfizer's vaccine side effects. Below are some crucial data released this week regarding natural immunity in children, COVID vaccine effectiveness, Pfizer's COVID pill, vaccine side effects, ect. The "post-authorization" adverse events list starts on page 30 of this document. Covid Vaccine Religious Exemption Documents. Comment. Reply. "1p36 deletion syndrome". FDA-CBER-2021-5683-0000083. They received an Pfizer-BioNTech COVID-19 Vaccine VRBPAC Briefing Document . Toggle navigation. BOMBSHELL: Pfizer Vaccine Study's Massive List Of "Adverse Events Of Interest" Starting on page 30 of a newly uncovered company document, an exhaustive list of serious adverse reactions to the shot is fully outlined. PFIZER DOCUMENT. In a shameless effort to bury the information, the FDA . PFIZER boss Albert Bourla has called a fourth booster dose of its Covid vaccine "necessary", despite the shocking revelation of 158,000 adverse events linked to the jab. The document was submitted by Pfizer as part of its Biological License Application (BLA) to the United States Federal Drug Administration (FDA) . The judge rejected the FDA's request for a slower release schedule citing the "paramount public importance" of the vaccine data. Search for: *blogg. They waited till the last minute to release them, so I cannot go through them tonight, but here is the link if anyone wants to begin looking for interesting information! A NOTE ABOUT THE FIRST ADVERSE EVENT CITED IN APPENDIX 1: 1p36 Deletion Syndrome Pfizer wanted you to wait till 2085 to know that the vaccine you took has 9 PAGES of side effects. In their lawsuit filed September 16, 2021, the plaintiffs asked the FDA to share the data it relied upon in licensing Pfizer's COVID vaccine. Pfizer Documents Reveal 8 Pages of Potential Side Effects. 2020 - February 28th, 2021. Now you know why they wanted to hide it. Pfizer/FDA first 30 pages: 1,227 deaths from December 1 to February 28 out of 42,086 reported cases: One in 34. Anyone may view our press releases, press statements, and press kits. 19) In this batch were no less than nine single-space pages of "adverse events of special interest," listed in alphabetical order 20 — 158,000 in all! 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