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 the FDA’s VAERS website for […]
CDC Ends VSAFE Website for Vaccine After-Effects Reporting, Page Now Reads ‘Thank You For Your Participation’
“Does this mean that the CDC believes that the mRNA Covid-19 injections are so safe, there is no need to monitor adverse event reports any longer?” Earlier this summer, the Centers for Disease Control and Prevention (CDC) stopped collecting data on the adverse effects of Covid-19 vaccines through the agency’s V-safe website. Now, rather than […]
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. August 15, 2023, update: The […]
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 mate, and they were even […]
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 PF-07302048 (BNT162B2) Received Through 28-FEB-2021 (a.k.a., […]
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 “black box.” (https://www.fda.gov/media/71866/download) Boxed Warnings […]
ICAN Warns FDA Advisory Committee of Serious Issues with Pfizer’s RSV Vaccine for Pregnant Women
On May 18, 2023, the FDA’s vaccine committee met to vote on whether Pfizer’s new RSV vaccine is “safe” and “effective.” Ahead of that meeting, ICAN, through its attorneys, wrote a letter to the FDA committee members to warn about numerous serious issues evident from its clinical trial, including the low efficacy, significant adverse events, and lack of a placebo […]
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 (BNT162B2) Received Through 28-FEB-2021 (a.k.a., “5.3.6“). […]
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, U.S. Presidential election. Regulatory licensure […]
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 came to understand Pfizer […]
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 employee, Robert T. Maroko, approved […]
Report 51: Liver Adverse Events – Five Deaths Within 20 Days of Pfizer’s mRNA COVID Injection. 50% of Adverse Events Occurred Within Three Days.
The War Room/DailyClout Pfizer Analysis Post-Marketing Group – Team 1 created the following Liver (i.e., Hepatic) System Organ Class (SOC) Review from data in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received Through 28-FEB-2021 (a.k.a., “5.3.6“). There were 70 patient cases with 94 adverse events reported in the hepatic SOC […]
FDA and Pfizer Data Allegedly Missing IMPORTANT Blood Brain Barrier Data – Letter
Dr. Peter Marks, Director of the Center for Biologics Evaluation and Research (CBER) Food and Drug Administration Dept. of Health and Human Services (HHS) Peter.Marks@fda.hhs.gov April 16, 2022 Dear Dr. Marks, I’ve just read an article stating highly inflammatory lipid nanoparticles (LNP)s “could be responsible for adjuvanticity and some of the side effects” of […]
What Did Pfizer and the FDA Know and When? Dr Wolf Explains Court-Released Pfizer Documents
What Did Pfizer and the FDA Know and When? | Guest: Naomi Wolf | 4/20/22 Conservative Review with Daniel Horowitz Today, we are joined by Naomi Wolf, founder of Daily Clout, to do a deep dive into the court-released Pfizer documents. Her team of scientists and doctors are poring over all of the 55,000 pages […]
NEW Pfizer Data Reveals Conflicts of Interest in Vaccine Trials
In September 2020, Dr. Anthony Fauci declared in an interview that the U.S. Food and Drug Administration’s Data and Safety Monitoring Board (DSMB) “is an independent body.” Clarifying further, he explained that the board—which offers expert advice to the FDA on a range of issues, including the approval of the Pfizer jab—is “beholden to no one, not to the president, […]
Latest Pfizer DATA DUMP Shows Natural Immunity WORKS, Vaccine Long Term Effects Still Unknown – Video
“Kim Iversen reviews newly released documents related to Pfizer’s Covid-19 vaccine research. According to the CDC people who were unvaccinated and did not have prior COVID-19 infection remain at the highest risk of infection and hospitalization. Those who were previously infected, both with or without prior vaccination, had the greatest protection. Additionally, a study by […]
Former BlackRock Fund Manager Edward Dowd Reveals Wall Street Now Paying Attention to the ‘Trust the Science’ Fraud
Blackrock’s Edward Dowd reveals Wall Street is now paying attention to the “trust the science” fraud. As Pfizer try to ‘pump their stock’ Hedge Fund guru Dowd takes us inside what he calls the third great fraud in his lifetime, in this new bombshell interview with Dr. Naomi Wolf. Watch the Full Interview Now! […]
FDA and Pfizer Knew COVID Shot Caused Immunosuppression
At A Glance April 1, 2022, another batch of 11,000 Pfizer documents were released by the U.S. Food and Drug Administration. Pfizer trial data reveal natural immunity was as effective as the jab, and that shot side effects were more severe in those under 55. Since the risk of severe COVID is dramatically lower […]
Pfizer to Ask US Regulators to Authorize COVID Vaccine Booster for Kids in 5–11 Age Group
Pfizer and BioNTech plan on asking the U.S. Food and Drug Administration (FDA) to grant emergency use authorization for a booster for their COVID-19 vaccine for children aged 5- to 11-years-old, the companies announced on April 14. Read Full Article Now
Pfizer Failed to Inform Us About These Vaccine Health Risks
Hindsight has finally arrived, and while still very murky, the fog of Covid is beginning to clear. As a flood of Pfizer documents is released from the FDA, we’ll learn in more detail how 2021 unfolded, who knew what when, and how harmful the vaccines actually are. The DailyClout/WarRoom Pfizer Document Review team of analysts […]