Report 78: Thirty-Two Percent of Pfizer’s Post-Marketing Respiratory Adverse Event Patients Died, Yet Pfizer Found No New Safety Signals.
The War Room/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1) – Joseph Gehrett, MD; Barbara Gehrett, MD; Chris Flowers, MD; and Loree Britt – wrote a compelling analysis of Respiratory Adverse Events of Special Interest (AESIs) found in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of …
Pfizer’s Comirnaty mRNA COVID Vaccine Manufacturing Has Dropped by 89% Due to Decrease in Demand
The Follow the Money Team’s new report on Pfizer’s financials, based on Pfizer’s Q1 2023 reporting, offers many important insights: Pfizer reports that its mRNA COVID vaccine, Comirnaty®, manufacturing activities, performed on behalf of BioNTech, dropped 89% to only $5 million quarter-over-quarter. In its Q1 2023 report, Pfizer assumes no …
Carol Taccetta, MD: “Boxed Warning,” the FDA’s Most Serious Warning, Is Absent from All COVID-19 Vaccine Fact Sheets
Introduction There are some adverse reactions in a product label that are so serious, and possibly even preventable, that special labeling is required to highlight this warning information: a “BOXED WARNING.” https://www.fda.gov/media/71866/download https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfCFR/CFRSearch.cfm?fr=201.57 This boxed warning information, “critical for a prescriber to consider,” is commonly referred to as a …
More Horrors, This Time From Moderna – Defending the Republic Lawsuit Obtains Almost 15,000 Pages of Moderna COVID-19 Vaccine Clinical Trial Documents
Defending the Republic on Its Historic Win to Require the FDA to Release Moderna’s Spikevax Clinical Trial Documentation “As a result of Defending the Republic’s (DTR) successful Freedom of Information Act (FOIA) litigation against the Food and Drug Administration (FDA), we are excited to announce that we are releasing nearly …
Carol Taccetta, MD, Requests References from CBER Director to Support CDC’s “[Building] Evidence” That Experimental Bivalent COVID-19 Vaccines Are “Safe and Effective” During Pregnancy and “Not Associated with Fertility Problems”
Introduction The CDC recommends “COVID-19 vaccination” to “people who are pregnant, breastfeeding, trying to get pregnant now, or those who might become pregnant in the future.” (https://www.cdc.gov/coronavirus/2019-ncov/vaccines/recommendations/pregnancy.html) Pfizer/BioNTech’s study, “To Evaluate the Safety, Tolerability, and Immunogenicity of BNT162b2 Against COVID-19 in Healthy Pregnant Women 18 Years of Age and …
Biased Media Coverage of RFK Jr. Endangers Fair Elections
President John F. Kennedy with his nephew, Robert F. Kennedy, Jr — The White House, c.1962 The single greatest risk to our electoral process is neither manipulation of the polls nor attacks undermining results; it is a press corps that covers candidates with a predetermined bias. The treatment of Robert …
Federal Judge Who Awarded Big Free Speech Win In Missouri v. Biden Denies Biden Regime’s Motion To Stay
The federal judge who issued a July 4 preliminary injunction blocking the Biden regime from colluding with Big Tech to censor Americans denied the administration’s motion to stay on Monday. Less than one week after he agreed the federal government appeared to lead “the most massive attack against free speech in United …
Report 77: Women Suffered 94% of Dermatological Adverse Events Reported in First 90 Days of Pfizer COVID “Vaccine” Rollout. 80% of These Adverse Events Were Categorized As “Serious.”
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 – produced a report about Dermatological Adverse Events of Special Interest (AESIs) found in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 …
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. ARVE Error: src mismatch provider: youtube url: https://www.youtube.com/watch?v=KgldG9r-i9M&ab_channel=Dr.JohnCampbell src in org: https://www.youtube-nocookie.com/embed/KgldG9r-i9M?feature=oembed&rel=0 src …
Report 76: Pfizer Had Data to Announce Its COVID-19 Vaccine’s Alleged “Efficacy” in October 2020. Why Did Pfizer Delay the Announcement Until November 9, 2020, Six Days After the 2020 U.S. Presidential Election?
Executive summary On July 21, 2020, the United States (U.S.) government, Pfizer, and BioNTech signed a contract, known as a Statement of Work (SOW), for the rapid development of and obtaining regulatory licensure for a COVID-19 vaccine by October 31, 2020, a few days prior to the November 3, 2020, …
Report 75: mRNA COVID “Vaccines” Have Created a New Class of Multi-Organ/System Disease: “CoVax Disease.” Children from Conception on Suffer Its Devastating Effects. – Histopathology Series – Part 4d
This report is Part 4d in a series. It follows Part 1, “Report 56: Autopsies Reveal Medical Atrocities of Genetic Therapies Being Used Against a Respiratory Virus;” Part 2, “Report 58: Part 2 – “Autopsies Reveal Medical Atrocities of Genetic Therapies Being Used Against a Respiratory Virus;” and Part 3, …
Report 74: Lipid Nanoparticles Corrupt Nature
INTRODUCTION This report delves into the history of lipid nanoparticles, as well as their use by pharmaceutical companies as a casing for mRNA in the COVID vaccines. It concludes that the use of the lipid nanoparticles to deliver mRNA causes widespread and significant harms to the human body. Without the …
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 …
Report 72: “Other AESIs” Included MERS, Multiple Organ Dysfunction Syndrome (MODS), Herpes Infections, and 96 DEATHS. 15 Patients Were Under Age 12, Including Six Infants.
The War Room/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1) – Joseph Gehrett, MD; Barbara Gehrett, MD; Chris Flowers, MD; and Loree Britt – wrote a report about Other Adverse Events of Special Interest (AESIs) found in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 …
Report 71: Musculoskeletal Adverse Events of Special Interest Afflicted 8.5% of Patients in Pfizer’s Post-Marketing Data Set, Including Four Children and One Infant. Women Affected at a Ratio of Almost 4:1 Over Men.
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 – wrote a review of musculoskeletal adverse events of special interest (AESIs) found in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 …
Report 70: Histopathology Series Part 4c – Autoimmunity: A Principal Pathological Mechanism of COVD-19 Gene Therapy Harm (CoVax Diseases) and a Central Flaw in the LNP/mRNA Platform
This report is Part 4c in a series. It follows Part 1, “Report 56: Autopsies Reveal Medical Atrocities of Genetic Therapies Being Used Against a Respiratory Virus;” Part 2, “Report 58: Part 2 – “Autopsies Reveal Medical Atrocities of Genetic Therapies Being Used Against a Respiratory Virus;” and Part 3, …
Report 69: BOMBSHELL – Pfizer and FDA Knew in Early 2021 That Pfizer mRNA COVID “Vaccine” Caused Dire Fetal and Infant Risks, Including Death. They Began an Aggressive Campaign to Vaccinate Pregnant Women Anyway.
The batch of Pfizer clinical trial documents released in April 2023 by the Food and Drug Administration (FDA) under court order contains a shocking, eight-page document titled, “Pregnancy and Lactation Cumulative Review.” The data in the Cumulative Review span “…from the time of drug product development to 28-FEB-2021.” A Pfizer …
Report 68: 34 Blood Vessel Inflammation, Vasculitis, Adverse Events Occurred in First 90 Days After Pfizer mRNA “Vaccine” Rollout, Including One Fatality. Half Had Onset Within Three Days of Injection. 81% of Sufferers Were Women.
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 – wrote an important review of vasculitis adverse events found in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received Through …
Follow-Up to “NAATs Used in Pfizer Clinical Trial to Test Asymptomatic Patients Despite Not Being Approved (or Even Emergency Use Authorized) for Asymptomatic Testing.”
Addendum: Since publication of this piece on April 25, 2023, a new Pfizer document tranche (dated April 3, 2023, but available publicly in late April 2023) has been released, and it included, “Report on Method Validation of a Cepheid Xpert® Xpress PCR Assay to Detect SARS-CoV-2.” The validation report states: “This report …
Ohio Governor Mike DeWine’s Financial Incentives for COVID-19 Vaccination
After the rollout of the mRNA COVID vaccines in December 2020, Ohio Governor Mike DeWine (R-OH) began creating “incentive programs” to entice the 11,764,342 residents of Ohio to take the experimental mRNA COVID-19 vaccines. How did so many Ohioans receive the dangerous mRNA COVID vaccine? You may be surprised to …