A study by New Zealand’s Beverley Lawton et al. “proved” that receipt of the HPV vaccine reduced preterm births. However, when statistical sleuths questioned the data, the study was retracted, as it turned out that the findings were inverted. The story of the retraction is quite scandalous and is worth exploring! https://web.archive.org/web/20200930050420/https://retractionwatch.com/2020/09/23/a-wholly-frustrating-and-embarrassing-process-authors-retract-paper-on-hpv-vaccine-and-preterm-birth/ The study […]
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 90: 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 knew that during the first three months of Pfizer’s mRNA COVID-19 vaccine rollout, thousands of COVID cases were reported to Pfizer — among vaccinated people. The ‘COVID-19 Adverse […]
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 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 […]
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 […]
Report 86: Pfizer’s Clinical Trial ‘Process 2’ COVID Vaccine Recipients Suffered 2.4X the Adverse Events of Placebo Recipients; ‘Process 2’ Vials Were Contaminated with DNA Plasmids.
Process 2 was hidden all along in Pfizer’s COVID ‘vaccine’ clinical trial, and the War Room/DailyClout investigators’ findings about it are mind-blowing. The Food and Drug Administration (FDA) knew that the Process 2 subjects had very high levels of adverse events, but there is no evidence that the agency acted […]
Part 2: The Alarming LNP (Lipid Nanoparticles) History You Haven’t Been Shown – the LNP Developers’ Own Studies Dating Back 20 Years
Part 1 is available here. This post includes the Table of Contents and sections A and B (twelve pages)of the LNP Files. Sections D through G (also twelve pages) will be posted within the week. ### Table of Contents (modified for LNP files release on SubStack): A. Introduction and Overview of […]
Part 1: The Alarming LNP (Lipid Nanoparticles) History You Haven’t Been Shown – the LNP Developers’ Own Studies Dating Back 20 Years
Introduction and Executive Brief sent to lawmakers & state investigators this summer. The below work was written from March to May 2023; after working with attorneys and physicians to bring this information to the attention of our lawmakers, the below introduction and eight-page Executive Brief/synopsis accompany a 90-page executive summary […]
Report 83: 23% of Vaccinated Mothers’ Fetuses or Neonates Died. Suppressed Lactation and Breast Milk Discoloration Reported.
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 shocking analysis of the “Use in Pregnancy and Lactation” section found in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of […]
CDC Now Refusing New COVID Vaccine Adverse Event Reports in Its V-Safe Program
The Centers for Disease Control and Prevention (CDC) V-safe website quietly stopped collecting adverse event reports with no reason or explanation. The V-safe website simply states: “Thank you for your participation. Data collection for COVID-19 vaccines concluded on June 30, 2023.” If you go there today, V-safe directs users to […]
US Government COVID-19 Genetic “Vaccine” Databases: Sloppy or Corrupt? Or Both?
Defense Military Epidemiology Database (DMED), Vaccine Adverse Events Reporting Systems (VAERs), and v-safe have numerous irregularities. Responsibility diffusion and secrecy have been employed to protect those involved. Lymphocytic infiltration of the myometrium (muscle layer) following COVID-19 spike-producing drugs. (Burkhardt Group Collection) It is not surprising to observe the […]
“To Evaluate the Safety, Tolerability, and Immunogenicity of BNT162b2 Against COVID-19 in Healthy Pregnant Women 18 Years of Age and Older” – Latest version (submitted July 14, 2023) on ClinicalTrials.gov
“The Safety of BNT162b2 Against COVID-19 in Healthy Pregnant Women 18 Years of Age and Older,” eh? Hmm. I was under the impression that if you are pregnant, or hoping to be, you shouldn’t do certain things like drink alcohol, smoke cigarettes, and get injected with experimental transfecting agents. You […]
Artist Ellen Danforth Embroiders Illustration for Pfizer Reports Book Report 18: “What Did Pfizer Know, and When Did They Know It? Neurological Harms Concealed.”
DailyClout is honored that artist Ellen Danforth is working with artist Rebecca Soudant to illustrate reports from the War Room/DailyClout Pfizer Documents Analysis Reports book. Ms. Danforth embroidered the lovely piece shown in the image above as an illustration of Pfizer Report 18 in the book, “What Did Pfizer […]
International Experts Testify Again, This Time in Brazil (Porto Alegre Seminar)
The brave representative Fernanda Barth led the hearing in the Municipality of Porto Alegro along with John Kage. Many of the names you have come to love and respect were there, and I was asked by Dr Naomi Wolf to represent the 3,500 volunteers of the WarRoom/DailyClout Pfizer Document Investigations. […]
Report 80: Moderna mRNA COVID-19 Injection Damaged Mammals’ Reproduction: 22% Fewer Pregnancies; Skeletal Malformations, Pain, Nursing Problems in Pups. FDA Knew, Yet Granted EUA.
Based on “A GLP intramuscular combined developmental and perinatal/postnatal reproductive toxicity study of mRNA-1273 in rats. FDA-CBER-2-22-4207-0015,” Moderna’s COVID-19 mRNA drug damaged the reproductive systems of female rats their estrous cycles (the recurring period of sexual receptivity and fertility in many female mammals) were disturbed, they were less likely to […]
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 […]
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 […]