To The Editor, While articles by The Telegraph reveal how the VDPS (Vaccine Damage Payment Scheme) has failed many struggling with lost family members and life-changing injuries caused by Covid vaccines, more in-depth reporting is needed to further examine and inform the public of this unfair and not fit for […]
Report 86: Pfizer’s Clinical Trial ‘Process 2’ COVID Vaccine Recipients Suffered 2.4X the Adverse Events of Placebo Recipients; ‘Process 2’ Vials Were Contaminated with DNA Plasmids.
Process 2 was hidden all along in Pfizer’s COVID ‘vaccine’ clinical trial, and the War Room/DailyClout investigators’ findings about it are mind-blowing. The Food and Drug Administration (FDA) knew that the Process 2 subjects had very high levels of adverse events, but there is no evidence that the agency acted […]
472 Pages FOIAed from CDC Leaders, 2021, Reveal Lengthy Comms Re: ‘Myocarditis,’ Massive Redactions. CDC Hiding April 2021 Monthly Safety Report on Pfizer’s Vaccine and Myocarditis/Pericarditis.
Attorney Edward Berkovich submitted a Freedom of Information Act (FOIA) request to the Centers for Disease Control and Prevention (CDC) stating, “I request emails sent by and received by Dr. Rochelle P. Walensky, Sherri A. Berger, and Kevin Griffis (all of whom are CDC personnel) on dates beginning February 1, […]
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 […]
United Kingdom Health Agency Gets FOIA Requesting All AstraZeneca COVID-19 Vaccine Data
A legally-produced, effective Freedom of Information Act (FOIA) request was sent to Dame June Raine, Chief Executive of Medicines and Healthcare Products Regulatory Agency (MHRA), on behalf of the Health Advisory and Recovery Team (HART), requesting that the MHRA fully produce all the data, information and documents submitted to them by AstraZeneca […]