A Major Book Launches, Revealing a Massive Scandal, and Grotesque Attacks Begin Listen to the audio version of this essay here. So, it begins. The WarRoom/DailyClout Pfizer Documents Research Volunteers have produced 51 stunning reports, compiling all of their findings from their months-long review and analysis of the Pfizer documents, […]
Report 51: Liver Adverse Events – Five Deaths Within 20 Days of Pfizer’s mRNA COVID Injection. 50% of Adverse Events Occurred Within Three Days.
The War Room/DailyClout Pfizer Analysis Post-Marketing Group – Team 1 created the following Liver (i.e., Hepatic) System Organ Class (SOC) Review from data in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received Through 28-FEB-2021 (a.k.a., “5.3.6“). There were 70 patient cases with 94 adverse events […]
By Eliminating Requirement for Animal Testing, FDA Modernization Act Allows Faster, More Cost-effective Drug Development
By easing regulatory requirements for animal testing, the Act allows scientists to use innovative, leading-edge technologies more fully in future drug development strategies. By ROBERT ASPBURY Congress passed the FDA Modernization Act 2.0 last week removing the requirement to use animal testing in drug development. This will allow drug companies the […]
Letter to the FDA: COVID-19 ‘Vaccines’ and COVID-19 Infection Linked to Myocarditis – What Do They Have in Common?
Peter Marks, MD, PhD Director, Center for Biologics Evaluation and Research U.S. Food and Drug Administration 10903 New Hampshire Avenue WO71-7232 Silver Spring, MD 20993 Peter.Marks@fda.hhs.gov December 18, 2022 Dear Dr. Marks, I am troubled by the following, and look forward to your studied response on my single […]
Pfizer/BioNTech Trial – A failed yet in depth attempt to reproduce the NEJM & FDA efficacy figures
Study version 1.3, published on 2022-12-09 To view the full version with graphics, please click here. Introduction We review, in this article, a list of problems in the Pfizer/BioNTech C4591001 Trial, which came out in our attempts to reproduce the results provided by the study. Using the sponsor’s data communicated to […]
Report 49: Clotting System-Related Adverse Events Following Pfizer COVID-19 mRNA Vaccination
The War Room/DailyClout Pfizer Documents Analysis Project Post-Marketing Team created the following Thromboembolic System Organ Class (SOC) Review from data in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received Through 28-FEB-2021 (a.k.a., “5.3.6“). The thromboembolic system is the human body’s clotting system and includes general […]
FOIA’d Contracts Show CDC Expected up to 1,000 VAERS Reports per Day for COVID Vaccines
Executive Summary In late August 2020, the CDC contracted with General Dynamics to handle VAERS reports for COVID-19 vaccines. The contract anticipated up to 1,000 reports per day, with up to 40% of them serious in nature. The value of the year-long contract was $9.45 million. This means that months […]
“170 Patients That Changed Everything” – Spectator | Australia
Few people realise that the Emergency Use Authorisation (EUA) of the Pfizer-BioNTech Covid-19 Vaccine/BNT162b2 was granted on the efficacy data of 170 patients. The 162 who received a placebo and 8 patients who were vaccinated formed the basis of the 95 per cent efficacy claims. There has not been much […]
Report 46: How Many Pregnant Women Received LNP/mRNA via COVID-19 Vaccine During the Year 2021? Only Estimates Are Available.
Shockingly, as 2022 comes to a close and the world reaches the two-year mark of experimental COVID-19 vaccines being available to the general public, the scientific and medical communities, as well as everyday citizens, still have very little information about the effects of mRNA COVID-19 vaccines on pregnant women and […]
A Drug Safety Physician’s Correspondence with the FDA: A Quest for Accuracy in Investigational Bivalent mRNA COVID-19 ‘Vaccine’ Adverse Event Reporting
Introduction On November 4, 2022, the Centers for Disease Control and Prevention (CDC) and U.S. Food and Drug Administration (FDA) concluded that, based on Vaccine Adverse Events Reporting System (VAERS) and v-safe data received between August 31, 2022, and October 23, 2022, “Health care providers and patients can be […]
Did You Know? Thousands of Adverse Events Since Pfizer mRNA Vaccine Rollout
Video by Dr. Chris Flowers The data in this video is from Pfizer’s “post marketing” document, which is titled, “5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021.” The analysis in Pfizer’s post marketing document was completed on February 28, 2021. Its appendix shows 1290 […]
An Open Letter to Wellesley’s President
Your Bivalent Booster Mandate For Students is Inappropriate I’m pleased to share an open letter to Wellesley’s president by Dr. David McCune. His last post was about the Pfizer vaccine. If you agree, you can add your signature at the link below. Vinay Prasad MD MPH Dear President Johnson, Recently, a Wellesley […]
Bombshell Emails: CDC Pressured FDA to Authorize COVID Boosters Without Clinical Trials
The Centers for Disease Control and Prevention pressured U.S. regulators to clear COVID-19 boosters without clinical trial data, according to emails obtained by Judicial Watch. The Centers for Disease Control and Prevention (CDC) pressured U.S. regulators to clear COVID-19 boosters without clinical trial data, according to newly released emails. CDC officials […]
Letter to the FDA: Vaccine-Induced Immune Thrombotic Thrombocytopenia (VITT), a New and Dangerous Syndrome from Certain COVID Vaccines – Do We Have Them All?
Introduction WHAT IS “VITT”? Vaccine-induced Immune Thrombotic Thrombocytopenia (VITT) is “a newly described syndrome” “characterized by new onset thrombocytopenia [i.e., low blood platelet count] and acute venous or arterial thrombosis [i.e., blood clot], including at unusual sites such as the cerebral venous sinus, with onset of symptoms approximately […]
Amy Kelly on Just Think Podcast: Combing The Data & Sounding The Alarms
This week, Amy Kelly, COO of Daily Clout and the Program Director for the Pfizer Documents Analysis Project, oversees the approximately 3,250 volunteers who are reviewing, analyzing, and reporting on the court-ordered, FDA-released Pfizer documents, as well as the approximately 350 volunteer attorneys who are identifying legal actions to be […]
Report 45: Failure of Serialization By Pfizer Flouted Established Pharma Industry Rules
Introduction: There are strict protocols in place regarding the storage and distribution of all pharmaceuticals to ensure safety throughout the delivery process. Particularly for mRNA Covid vaccines that were distributed by billions worldwide, those protocols should have been carefully practiced. Dr. Chris Flowers has reported that not only were standard […]
Professor William Robinson’s letter to administrators at UCSB
Professor Robinson will be silent no more. He wants to “encourage the broadest possible public debate” on compulsory COVID-19 vaccination. I am a professor at the University of California at Santa Barbara (UCSB). On October 2nd, I sent a letter to administrators in response to an announcement that recently mandated […]
Today’s Legislative Call to Action: FDA Ethics Act of 2022
HB 8828 FDA Ethics Act of 2022 US Congress 117th Congress About HB-8828 To address potential conflicts of interest among entities serving as Food and Drug Administration contractors, and for other purposes. Conflicts of interest are ok as long as they are disclosed. No prohibition against licensing agreements with […]
Reading, Understanding, and Interpreting Medical and Scientific Literature – Assisting the Neophyte.
Recently Modern Discontent published a paper on Substack that proves to be a worthwhile guide for those new to reading medical and scientific literature. “Modern” represents himself/herself as a: “Disaffected Scientist, Disaffected Liberal. Trying to make sense of things and ranting about science, culture, and the world beyond.” https://moderndiscontent.substack.com/p/how-i-tackle-reading-papers […]
Amy Kelly: What Did The Hundreds of Thousands of Pfizer Documents From the FDA Expose?
Amy Kelly addresses the Australian Medical Professionals Society and their Reclaiming Medicine Event. AMY KELLY Amy Kelly is the Program Director for the War Room/DailyClout Pfizer Documents Analysis Project. She oversees the approximately 3,250 volunteers who are reviewing, analyzing, and reporting on the court-ordered, FDA-released Pfizer documents, as well as […]