Internal Report 29: “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,…

Internal Report 34: “100s of Possible Vaccine-Associated Enhanced Disease (VAED) Cases in First 3 Months of Pfizer’s mRNA COVID Vaccine Rollout, Yet Public Health Spokespeople Minimized Their Severity by Calling Them ‘Breakthrough Cases.’”

By late February 2021, a group of experts called Brighton Collaboration released a paper, which was published in…

Internal Report 33: “FDA Based Moderna’s mRNA COVID Vaccine Approval on Test of a Completely Different Non-COVID Vaccine. Only Males Included in Test.”

Moderna researchers did not test their COVID-19 mRNA drug, called SPIKEVAX, to find out where it would go…

Internal Report 32: “Pfizer’s ‘Post-Marketing Surveillance’ Shows mRNA-Vaccinated Suffered 1000s of COVID Cases in 1st 90 Days of Vaccine Rollout. Most Infections in the Vaccinated Categorized as ‘Serious Adverse Events.’”

Though spokespeople assured us that the COVID-19 injection stops—well—COVID, Pfizer and the Food and Drug Administration (FDA) both…

Internal Report 31: “WarRoom/DailyClout Researchers Find Pfizer Delayed Recording Vaccinated Deaths at Critical Juncture of EUA Process. Improper Delays in Reporting Deaths in the Vaccinated Led FDA to Misstate Vaccine’s Effectiveness, Influenced EUA Grant Decision.”

On September 5, 2023, DailyClout reported that a WarRoom/DailyClout Research Team—Corinne Michels, PhD; Daniel Perrier; Jeyanthi Kunadhasan, MD;…