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 […]
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 […]
“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 […]
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, […]
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 […]
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 […]
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 […]
Did You Know? Thousands of Adverse Events Since Pfizer mRNA Vaccine Rollout
Video by Dr. Chris Flowers The data in this video is from Pfizer’s “post marketing” document, which is titled, “5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021.” The analysis in Pfizer’s post marketing document was completed on February 28, 2021. Its appendix shows 1290 […]
An Open Letter to Wellesley’s President
Your Bivalent Booster Mandate For Students is Inappropriate I’m pleased to share an open letter to Wellesley’s president by Dr. David McCune. His last post was about the Pfizer vaccine. If you agree, you can add your signature at the link below. Vinay Prasad MD MPH Dear President Johnson, Recently, a Wellesley […]
Bombshell Emails: CDC Pressured FDA to Authorize COVID Boosters Without Clinical Trials
The Centers for Disease Control and Prevention pressured U.S. regulators to clear COVID-19 boosters without clinical trial data, according to emails obtained by Judicial Watch. The Centers for Disease Control and Prevention (CDC) pressured U.S. regulators to clear COVID-19 boosters without clinical trial data, according to newly released emails. CDC officials […]
Amy Kelly on Just Think Podcast: Combing The Data & Sounding The Alarms
This week, Amy Kelly, COO of Daily Clout and the Program Director for the Pfizer Documents Analysis Project, oversees the approximately 3,250 volunteers who are reviewing, analyzing, and reporting on the court-ordered, FDA-released Pfizer documents, as well as the approximately 350 volunteer attorneys who are identifying legal actions to be […]
Report 45: Failure of Serialization By Pfizer Flouted Established Pharma Industry Rules
Introduction: There are strict protocols in place regarding the storage and distribution of all pharmaceuticals to ensure safety throughout the delivery process. Particularly for mRNA Covid vaccines that were distributed by billions worldwide, those protocols should have been carefully practiced. Dr. Chris Flowers has reported that not only were standard […]
Professor William Robinson’s letter to administrators at UCSB
Professor Robinson will be silent no more. He wants to “encourage the broadest possible public debate” on compulsory COVID-19 vaccination. I am a professor at the University of California at Santa Barbara (UCSB). On October 2nd, I sent a letter to administrators in response to an announcement that recently mandated […]
Today’s Legislative Call to Action: FDA Ethics Act of 2022
HB 8828 FDA Ethics Act of 2022 US Congress 117th Congress About HB-8828 To address potential conflicts of interest among entities serving as Food and Drug Administration contractors, and for other purposes. Conflicts of interest are ok as long as they are disclosed. No prohibition against licensing agreements with […]
Amy Kelly: What Did The Hundreds of Thousands of Pfizer Documents From the FDA Expose?
Amy Kelly addresses the Australian Medical Professionals Society and their Reclaiming Medicine Event. AMY KELLY Amy Kelly is the Program Director for the War Room/DailyClout Pfizer Documents Analysis Project. She oversees the approximately 3,250 volunteers who are reviewing, analyzing, and reporting on the court-ordered, FDA-released Pfizer documents, as well as […]
CDC and FDA Misinformation – Retroactive Editing, Erroneous Spontaneous Abortion Rate Calculation, Obfuscation by NEJM
Breaking: Cause of Mortality and Injury to Infants and Fetuses caused by the Pfizer Injections Via Tainted Breast Milk and Compromised Placenta Membranes were Quashed by the US Health Agencies – an Esteemed Medical Journal Colluded – According to Pfizer Trial Document Experts Team's Analysis
Judicial Watch: New Documents Reveal COVID-19 Vaccine Studies Used by HHS were Conducted in China
(Washington, DC) – Judicial Watch announced today that it received 115 pages of records from the Department of Health and Human Services (HHS) revealing previously redacted locations of COVID-19 vaccine testing facilities in Shanghai, China. The Food and Drug Administration (FDA) had claimed the name and location of the testing facilities were protected by […]
