Career scientists are struggling with attention to detail in fulfilling their vaccine safety duties. Their conclusions, marked by errors and oversights, have led to lives lost and debilitating disorders, as proven by the government scientists’ own review documents. In spring 2021, the US Food and Drug Administration (FDA) granted emergency […]
FOIA’d CDC Emails Reveal Disturbing Myocarditis Timeline Warranting Investigation: Different Messaging Internally Vs. Publicly About COVID-19 Vaccines and Myocarditis.
“We don’t have any evidence to suggest a signal or a safety problem for myocarditis[.]” Dr. Tom Shimabukuro, CDC, April 19, 2021 Investigative work by two intrepid scientists, combined with Freedom of Information Act (FOIA) records, reveal a disturbing chronology during which the Centers for Disease Control and Prevention […]
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 […]
Hot Lots: “Batch-dependent safety of the BNT162b2 mRNA COVID-19 vaccine” by Schmeling et al.
Dr. John Campbell discusses a March 2023 Danish research paper with one of the paper’s authors, Dr. Vibeke Manniche. The paper demonstrates that early batches of COVID-19 “vaccines” were associated with very high levels of adverse events. Dr. Manniche’s research letter can be found here: https://onlinelibrary.wiley.com/doi/10.1111/eci.13998. (Schmeling, Max, et al. […]
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 […]