Dr. Fauci, Dr. Walensky, Dr. Vivek Murthy (the U.S. Surgeon General), and more than a dozen White House staffers were CC’d on emails confirming in February through April 2021 that minors were suffering heart damage from the mRNA COVID injections. Rather than disclosing this fact to Americans, the teams […]
Dr. Naomi Wolf: 300% Rise of COVID Deaths in Pregnant Women During Delta Appears To Implicate Vaccine-Associated Enhanced Disease (VAED) – Ask Dr. Drew
Researchers at Dr. Naomi Wolf’s DailyClout analyzed data from the American Medical Association’s 2021 maternal mortality report – and found alarming signs of harm to pregnant women and a disturbing increase of deaths during the Delta wave. “1,205 mothers who died in or within forty-two days of pregnancy in […]
Report 93: Pfizer’s ‘Post-Marketing Surveillance Report’ Reveals That Pfizer Manipulated Data and Wrongly Tabulated Adverse Events, Which Concealed Them.
We evaluated Pfizer’s 38-page “5.3.6 Cumulative Analysis of Post-Authorization Adverse Events Reports of PF-07302048 (BNT162b2) received through 28-Feb-2021,” commonly known as “5.3.6,” starting in September of 2022. Patterns emerged across the System Organ Classes (SOCs). These patterns included Pfizer’s apparent concealment of various cases of adverse events, as well as […]
Report 92: 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 Vaccine, clearly defining Vaccine-Associated Enhanced Disease (VAED), which is a more severe clinical presentation of a disease in a person vaccinated against that disease than would normally be seen in an unvaccinated person. Yet, […]
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 […]