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 […]
Supreme Court Decides Abortion Pill to Remain Amid Ongoing Legal Battle
The U.S. Supreme Court decided Friday that mifepristone, an abortion pill, will be broadly accessible amid an ongoing legal battle over its regulatory approval. Mifepristone, approved in 2000 by the Food and Drug Administration (FDA), is part of a chemical abortion process and is generally taken with another drug called […]
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 […]
FDA Lacks Adequate Safety Testing of Lipid Nanoparticles (LNPs) in COVID-19 Vaccines
Once more, FDA puts its zealous policy to vaccinate everyone ahead of health. As many are aware, both Pfizer’s and Moderna’s COVID-19 vaccines are designed with lipid nanoparticles (LNPs), which are essentially fatty droplets that surround, protect, and transport the mRNA into cells. The problem is that these LNPs have […]
NAATs Used in Pfizer Clinical Trial to Test Asymptomatic Patients Despite Not Being Approved (or Even Emergency Use Authorized) for Asymptomatic Testing.
Nasal swab nucleic acid amplification tests (NAATs) are “a type of viral diagnostic test for SARS-CoV-2, the virus that causes COVID-19.” [https://www.cdc.gov/coronavirus/2019-ncov/lab/naats.html and https://www.fda.gov/consumers/consumer-updates/covid-19-test-basics] Although certain NAAT tests have now been authorized for emergency use (EUA) for screening purposes (in asymptomatic persons), the three NAAT tests used at the time […]
Losing Control of the Controlled Clinical Trial in These Times of Emergency Use Authorization (EUA) Vaccines
Do you remember your high school science teacher explaining what a controlled experiment is? It is when just one thing is changed in the group receiving the experimental intervention (compared to the “control” group receiving standard or no treatment), then one waits to see if there is a difference in […]
“The Underground Railroad of Ivermectin”
Dr. Mary Talley Bowden joined the DailyClout to discuss her battle to treat patients properly Practicing Medicine Dr. Mary Talley Bowden is an ENT by trade. Dr. Bowden’s dedication to practicing medicine and treating her patients have led her down a path that few others have been willing to take […]
Pfizer’s Clinical Trial Had More Deaths After Vaccination than Placebo
The FDA would likely let Pfizer get away with literally almost anything. Clinical trials are supposed to be statistical comparisons. They are designed to compare the outcomes in the group receiving a novel product with the outcomes in the group receiving a placebo. The resulting statistics are then used to […]
“Public Opinion is Beast”
Mr. Brad Paquette is a State Representative for the 37th District of Michigan. In response to the Project Veritas video, Mr. Paquette sent an official letter to Pfizer, along with 15 other State Representatives. UPDATE: 16 Michigan State legislators sign letter demanding answers from @Pfizer regarding viral #DirectedEvolution video "Pfizer […]
Letter to the Massachusetts Attorney General: CDC and FDA May Have Violated Several State Criminal Statutes
Two Massachusetts attorneys, Patricia B. Doherty and Julie A. Piantedosi, wrote a letter to the Massachusetts Attorney General (AG), Andrea Campbell, stating: The Federal Government, Food and Drug Administration (FDA), and the Centers for Disease Control and Prevention (CDC) hid the Pfizer mRNA COVID vaccine’s known adverse event details – […]
Pixels, Bots and Human Cruelty
A Major Book Launches, Revealing a Massive Scandal, and Grotesque Attacks Begin Listen to the audio version of this essay here. So, it begins. The WarRoom/DailyClout Pfizer Documents Research Volunteers have produced 51 stunning reports, compiling all of their findings from their months-long review and analysis of the Pfizer documents, […]
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 […]
By Eliminating Requirement for Animal Testing, FDA Modernization Act Allows Faster, More Cost-effective Drug Development
By easing regulatory requirements for animal testing, the Act allows scientists to use innovative, leading-edge technologies more fully in future drug development strategies. By ROBERT ASPBURY Congress passed the FDA Modernization Act 2.0 last week removing the requirement to use animal testing in drug development. This will allow drug companies the […]
Letter to the FDA: COVID-19 ‘Vaccines’ and COVID-19 Infection Linked to Myocarditis – What Do They Have in Common?
Peter Marks, MD, PhD Director, Center for Biologics Evaluation and Research U.S. Food and Drug Administration 10903 New Hampshire Avenue WO71-7232 Silver Spring, MD 20993 Peter.Marks@fda.hhs.gov December 18, 2022 Dear Dr. Marks, I am troubled by the following, and look forward to your studied response on my single […]
Pfizer/BioNTech Trial – A failed yet in depth attempt to reproduce the NEJM & FDA efficacy figures
Study version 1.3, published on 2022-12-09 To view the full version with graphics, please click here. Introduction We review, in this article, a list of problems in the Pfizer/BioNTech C4591001 Trial, which came out in our attempts to reproduce the results provided by the study. Using the sponsor’s data communicated to […]
Report 49: Clotting System-Related Adverse Events Following Pfizer COVID-19 mRNA Vaccination
The War Room/DailyClout Pfizer Documents Analysis Project Post-Marketing Team created the following Thromboembolic 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“). The thromboembolic system is the human body’s clotting system and includes general […]
FOIA’d Contracts Show CDC Expected up to 1,000 VAERS Reports per Day for COVID Vaccines
Executive Summary In late August 2020, the CDC contracted with General Dynamics to handle VAERS reports for COVID-19 vaccines. The contract anticipated up to 1,000 reports per day, with up to 40% of them serious in nature. The value of the year-long contract was $9.45 million. This means that months […]
“170 Patients That Changed Everything” – Spectator | Australia
Few people realise that the Emergency Use Authorisation (EUA) of the Pfizer-BioNTech Covid-19 Vaccine/BNT162b2 was granted on the efficacy data of 170 patients. The 162 who received a placebo and 8 patients who were vaccinated formed the basis of the 95 per cent efficacy claims. There has not been much […]
Report 46: How Many Pregnant Women Received LNP/mRNA via COVID-19 Vaccine During the Year 2021? Only Estimates Are Available.
Shockingly, as 2022 comes to a close and the world reaches the two-year mark of experimental COVID-19 vaccines being available to the general public, the scientific and medical communities, as well as everyday citizens, still have very little information about the effects of mRNA COVID-19 vaccines on pregnant women and […]
A Drug Safety Physician’s Correspondence with the FDA: A Quest for Accuracy in Investigational Bivalent mRNA COVID-19 ‘Vaccine’ Adverse Event Reporting
Introduction On November 4, 2022, the Centers for Disease Control and Prevention (CDC) and U.S. Food and Drug Administration (FDA) concluded that, based on Vaccine Adverse Events Reporting System (VAERS) and v-safe data received between August 31, 2022, and October 23, 2022, “Health care providers and patients can be […]