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The Latest Shocking Details From the US Border
https://rumble.com/embed/v3m80j7/?pub=mbdkr Host Brian O’Shea will kick us off with a brief run-through of stories that may be off your radar but he thinks you should know about in the context of the Unrestricted Warfare currently being conducted against the United States by the People’s Republic of China (PRC). …
Report 88: 2.5 Months After COVID Vaccine Rollout, Pfizer Changed Criteria for ‘Vaccination Failure,’ Causing 99% of Reported Cases to Not Meet That Definition. 3.9% of Reported ‘Lack of Efficacy’ Cases Ended in Death in First 90 Days of Public Vaccine Availability.
The War Room/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1) – Barbara Gehrett, MD; Joseph Gehrett, MD; Chris Flowers, MD; and Loree Britt – penned a telling analysis of the “Vaccine Effectiveness” Safety Concern section found in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 …
Three Critical Perspectives on the War in Israel and Palestine, Ukraine, and U.S. Global Strategy – Or Lack Thereof
Dear DailyClout, Could there be echoes of FDR and Pearl Harbor with respect to Israel’s alleged “intelligence failure” on October 7th? Can the U.S. fund and back two major wars – Gaza and Ukraine – at the same time? Will U.S. taxpayer-funded arms sent to Ukraine end up in the …
ICAN Attorneys File Major Lawsuit to Strike Down Portions of the PREP Act
ICAN is excited to announce that it is supporting a lawsuit that was filed today by ICAN’s attorneys to strike down the immunity to liability and the Countermeasures Injury Compensation Program (CICP) provisions of the PREP Act because they violate the constitutional rights of those injured or killed by a COVID-19 vaccine. As ICAN …
Report 87: In Early 2021, Pfizer Documented Significant Harms and Deaths Following Vaccination with Its mRNA COVID Vaccine. The FDA Did Not Inform the Public.
INTRODUCTION “5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162b2) Received Through 28-Feb-2021,” Pfizer’s post-marketing report, a required U.S. Food and Drug Administration (FDA) compliance document, is one of the ways in which the FDA assessed patients’ risks associated with Pfizer’s COVID-19 vaccine, BNT162b2. The data within the …
