Dr. Chris Flowers, MD, represented the WarRoom/DailyClout Pfizer and Moderna Documents Analysis Project volunteers at the International COVID Summit 6 (ICS6) conference in late September in Tokyo as well as in Japan’s House of Representatives. His focus was on the hidden deaths during the clinical trial and clinical trial deletions, […]
Dr. Jeyanthi Kunadhasan, WarRoom/DailyClout Researcher, Alerts the Therapeutic Goods Administration That Pfizer Had More Vaccinated Deaths Than Placebo Deaths in Its COVID Vaccine Clinical Trial
Dr. Jeyanthi Kunadhasan, an anaesthetist and perioperative physician in Australia and Treasurer of the Australian Medical Professionals’ Society, wrote to Dr. Tony Lawler, Deputy Secretary of Australia’s Therapeutic Goods Administration (TGA), on March 21, 2024, regarding the vaccinated deaths in Pfizer’s C4591001 COVID-19 vaccine clinical trial. Specifically, Dr. Kunadhasan explained […]
Report 98: FDA Selected Its ‘Vaccines Advisory Committee’ – Not Its Gene Therapy Advisory Committee – to Recommend the COVID Injections for Emergency Use, to Hide the Fact that the Products Are Not Vaccines But Gene Therapies
COVID-19 ‘vaccine’ drugs are modified mRNA gene therapy products. So, why did the FDA assign the review and recommendation responsibilities to the Vaccines and Related Biological Products Committee (VRBPAC) instead of the Cellular Tissue and Gene Therapy Advisory Committee (CTGTAC)? CTGTAC was the logical FDA advisory committee for such a […]
BREAKING: WARROOM/DAILYCLOUT VOLUNTEERS, OTHER EXPERTS, SAVE BRAZILIAN CHILDREN VIA SENATE TESTIMONY!
The hearings affected the Senate. Following eight hours of intense testimony from both doctors from Brazil and a contingent of international doctors, The Federal Senate of Brazil voted to suspend the mandates on 6-month – 5-year-old children that had been imposed upon them by the Lula administration. Dr. Chris Flowers […]
Report 96: mRNA COVID-19 Shots – ‘Vaccines’ or Gene Therapy Products? – Part 2
When considering a drug for emergency use authorization (EUA), the Food and Drug Administration (FDA) selects an internal advisory committee to review information and data submitted to the FDA by the pharmaceutical company about its new drug. These influential FDA advisory committees, based on that information and data, make recommendations […]
Letter to Texas Attorney General Ken Paxton: Vaccinated Deaths in Pfizer’s COVID Vaccine Clinical Trial Not Disclosed to FDA with EUA Data.
Dr. Jeyanthi Kunadhasan Team 3 DailyClout P.O. Box 24 Millerton, NY 12546 The Honourable Ken Paxton Attorney General of Texas (469) 247-2360 P.O. Box 3476 McKinney, Texas 75070 RE: Undisclosed Deaths in C4591001 Trial at the Vaccine and Related Biological Products Advisory Committee (VRBPAC) on December 10, […]
Report 94: Pfizer Secretly Studied a Heart Damage Marker, Troponin I, in Five- to 15-Year-Olds, Following mRNA COVID Vaccination in 2021.
We warned that there was proof that the Pfizer BNT162b2 mRNA COVID vaccine caused heart damage in teens and young adults, as early as May of 2021. As more information surfaces from the court-mandated release of Pfizer clinical trial documents by the FDA, and via FOIA’d emails, the CDC’s cover-up […]
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 […]
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 […]