Introduction and Executive Brief sent to lawmakers & state investigators this summer. The below work was written from March to May 2023; after working with attorneys and physicians to bring this information to the attention of our lawmakers, the below introduction and eight-page Executive Brief/synopsis accompany a 90-page executive summary […]
Report 84: War Room/DailyClout Research Team Breaks Huge Story: More Cardiovascular Deaths in Vaxxed Than Unvaxxed; Pfizer Did Not Report Adverse Event Signal; Death Reporting Delays Favored Pfizer/Vaccinated.
War Room/DailyClout Pfizer Documents Analysis team members Corinne Michels, PhD; Daniel Perrier; Jeyanthi Kunadhasan, MD; Ed Clark, MSE; Joseph Gehrett, MD; Barbara Gehrett, MD; Kim Kwiatek, MD; Sarah Adams; Robert Chandler, MD; Leah Stagno; Tony Damian; Erika Delph; and Chris Flowers, MD have published a bombshell study titled, “Forensic Analysis […]
International Experts Testify Again, This Time in Brazil (Porto Alegre Seminar)
The brave representative Fernanda Barth led the hearing in the Municipality of Porto Alegro along with John Kage. Many of the names you have come to love and respect were there, and I was asked by Dr Naomi Wolf to represent the 3,500 volunteers of the WarRoom/DailyClout Pfizer Document Investigations. […]
Carol Taccetta, MD: “Boxed Warning,” the FDA’s Most Serious Warning, Is Absent from All COVID-19 Vaccine Fact Sheets
Introduction There are some adverse reactions in a product label that are so serious, and possibly even preventable, that special labeling is required to highlight this warning information: a “BOXED WARNING.” https://www.fda.gov/media/71866/download https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfCFR/CFRSearch.cfm?fr=201.57 This boxed warning information, “critical for a prescriber to consider,” is commonly referred to as a […]
Report 76: Pfizer Had Data to Announce Its COVID-19 Vaccine’s Alleged “Efficacy” in October 2020. Why Did Pfizer Delay the Announcement Until November 9, 2020, Six Days After the 2020 U.S. Presidential Election?
Executive summary On July 21, 2020, the United States (U.S.) government, Pfizer, and BioNTech signed a contract, known as a Statement of Work (SOW), for the rapid development of and obtaining regulatory licensure for a COVID-19 vaccine by October 31, 2020, a few days prior to the November 3, 2020, […]
Report 73: Pfizer Knew by November 2020 That Its mRNA COVID Vaccine Was Neither Safe Nor Effective. Here Is What Pfizer’s Employees and Contractors Knew and When They Knew It.
Introduction Through the review of two documents – Pharmacovigilance Plan for Biologic License Application #125742 Of Covid-19 mRNA vaccine (nucleoside modified) (BNT162b2, PF-07302048) and 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162b2) Received Through 28-Feb-2021 – referred to below as “PV” and “5.3.6,” the contributors to this […]
YouTube REMOVED Dr. Flowers Testimony on Informed Consent, Restricts Account
On Saturday, April 22nd, Dr Chris Flowers MD gave testimony as an expert witness after being asked by the National Citizen’s Inquiry in Canada about the findings of the WarRoom/DailyClout Pfizer Document Investigators. This was the third day of the hearings in Saskatoon. The hearings were streamed live and uploaded […]
Losing Control of the Controlled Clinical Trial in These Times of Emergency Use Authorization (EUA) Vaccines
Do you remember your high school science teacher explaining what a controlled experiment is? It is when just one thing is changed in the group receiving the experimental intervention (compared to the “control” group receiving standard or no treatment), then one waits to see if there is a difference in […]
Report 50: 20% of Post-Jab Strokes Fatal in the 90 Days Following Pfizer COVID mRNA Vaccine Rollout
The War Room/DailyClout Pfizer Documents Analysis Project Post-Marketing Team created the following Stroke 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 stroke category comprises the diagnoses of strokes attributed to either […]
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 […]
“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 […]
UK Public Health Agency Approves COVID-19 vaccine for Babies Age Six Months- Four Years
The Medicines and Healthcare products Regulatory Agency (MHRA), a public health agency in the UK has signed its approval on administering COVID mRNA vaccines to babies from the age of six months old. The mRNA vaccine will be given at a smaller dose than the older age groups, and still […]
Letters to Dr. Walensky and her Rabbi
Dr. Robert L. Berkowitz, M.D., belongs to the same Congregation as Dr. Rochelle Walensky, the Director of the CDC. Back in June, when ACIP was preparing to vote on approving the Covid vaccines for babies as young as 6 months, Dr. Berkowitz sent a letter to Dr. Walensky, with their […]
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 […]
ACIP committee approves mRNA vaccines for the childhood schedule 15-0
We all predicted this would happen. This allows the EUA to end, but provides full immunity protection forever for the COVID vaccine manufacturers. This just happened minutes ago. The ACIP committee voted on Thursday, as predicted, to add the COVID vaccines to the childhood vaccination schedule so that the manufacturers […]
Videos: How Pfizer’s EUA Was Granted Based on Fewer Than 0.4% of Clinical Trial Participants
The videos linked below offer audio-visual explanations of Report 42: Pfizer’s EUA Granted Based on Fewer Than 0.4% of Clinical Trial Participants. FDA Ignored Disqualifying Protocol Deviations to Grant EUA. These videos show: 1. The pivotal Pfizer trial upon which the Emergency Use Authorization (EUA) for the COVID -19 vaccines […]
Report 42: Pfizer’s EUA Granted Based on Fewer Than 0.4% of Clinical Trial Participants. FDA Ignored Disqualifying Protocol Deviations to Grant EUA.
Locations of the 170 Pfizer Clinical Trial Patients Used to Gain Emergency Use Authorization (EUA) for Its COVID mRNA Vaccine. Courtesy of OPENVAET.org For audio-visual explanations of this report, please see these videos. So much has been written about the pivotal Pfizer Trial for COVID-19 (C4591001), that it is sometimes […]
Report 40: Data Do Not Support Safety of mRNA COVID Vaccination for Pregnant Women
Commentary on “Preliminary Findings of mRNA Covid Vaccine Safety in Pregnant Persons” as Reported by the Centers for Disease Control and Prevention and the Food and Drug Administration, June 17, 2021, New England Journal of Medicine Note: On September 26, 2022, Dr. Chandler published a follow-up report to the report […]
DailyClout and HFDF – Notice to Ascension Hospital Regarding Remdesivir
Most Americans know that remdesivir was granted EUA authorization by the FDA for adults and children for the treatment of COVID-19 patients and then later fully approved for both adults, and children as young as 28 days old. What most Americans don’t know is that remdesivir is a dangerous drug […]