Impact of COVID-19 State of Emergency on Female Reproduction
Overview In partnership with Kaleidoscope Strategic, DailyClout presents a unique and compelling analysis of medical health data. The analysis of about six million unique patients’ data highlights the negative reproduction impacts — including serious menstrual harms and female and male fertility issues — of Canada’s COVID-19 state of emergency and rollout …
Dr. Jeyanthi Kunadhasan, WarRoom/DailyClout Researcher, Alerts the Therapeutic Goods Administration That Pfizer Had More Vaccinated Deaths Than Placebo Deaths in Its COVID Vaccine Clinical Trial
Dr. Jeyanthi Kunadhasan, an anaesthetist and perioperative physician in Australia and Treasurer of the Australian Medical Professionals’ Society, wrote to Dr. Tony Lawler, Deputy Secretary of Australia’s Therapeutic Goods Administration (TGA), on March 21, 2024, regarding the vaccinated deaths in Pfizer’s C4591001 COVID-19 vaccine clinical trial. Specifically, Dr. Kunadhasan explained …
Report 98: FDA Selected Its ‘Vaccines Advisory Committee’ – Not Its Gene Therapy Advisory Committee – to Recommend the COVID Injections for Emergency Use, to Hide the Fact that the Products Are Not Vaccines But Gene Therapies
COVID-19 ‘vaccine’ drugs are modified mRNA gene therapy products. So, why did the FDA assign the review and recommendation responsibilities to the Vaccines and Related Biological Products Committee (VRBPAC) instead of the Cellular Tissue and Gene Therapy Advisory Committee (CTGTAC)? CTGTAC was the logical FDA advisory committee for such a …
‘We’re open for business’: FDA’s Peter Marks says agency ready to review novel cancer vaccines despite unknowns
As new cancer vaccines—led by Moderna and Merck’s mRNA-4157—near pivotal trial readouts, the FDA’s vaccines czar Peter Marks, M.D., Ph.D., said the agency is ready to review the shots despite AI-related unknowns. “We are ready to review—we’re open for business,” Marks, director of the FDA’s Center for Biologics Evaluation and …
Report 97: Pfizer Obscured Myocarditis Safety Signal Specific to Young Men. FDA Took Five Months to Notice Pfizer’s Obfuscation.
Career scientists are struggling with attention to detail in fulfilling their vaccine safety duties. Their conclusions, marked by errors and oversights, have led to lives lost and debilitating disorders, as proven by the government scientists’ own review documents. In spring 2021, the US Food and Drug Administration (FDA) granted emergency …
BOMBSHELL DATA FROM PFIZER, MODERNA, AND V-SAFE DATA Death and Destruction With Amy Kelly
Rob Nobrega and DailyClout COO and WarRoom/DailyClout Pfizer Documents Research Team Director Amy Kelly review the findings in the Pfizer documents, how the Moderna and Pfizer ages 12-15 are being released now and will continue to be released through the end of June 2025, updates found in the first batch …
Press Release: Almost 5,600 Pages of Moderna ‘Spikevax’ COVID Vaccine Animal Studies Released by FDA, Serious Adverse Events
DEFENDING THE REPUBLIC OBTAINS MODERNA DOCUMENTS February 28, 2024 – Today, Defending the Republic (DTR) is releasing nearly 5,600 pages of animal studies submitted by Moderna to the FDA in support of the approval of its COVID-19 vaccine “Spikevax.” This is the most significant and largest release of Moderna’s COVID-19 vaccine …
V-Safe Voices: Tachycardia Post-COVID Vaccination
DailyClout Introduces a New Series: “V-Safe Voices” The Centers for Disease Control and Prevention (CDC) uses V-safe to monitor vaccine safety. After signing up, V-safe participants share, through an app, with the CDC how they or their dependent(s) feel after getting a participating vaccine, including the COVID-19 vaccines. The app presents …
FDA Approves First Vaccine for Pregnant Women to Prevent RSV in Infants Six Months Old and Younger
Remember just a few short years ago when Americans were told that pregnant women should take as few medications as possible? On August 21, 2023, the United States Food and Drug Administration (FDA) approved an RSV (Respiratory Syncytial Virus) vaccine, Pfizer’s Abrysvo, for use in pregnant women at 32- to …
Report 96: mRNA COVID-19 Shots – ‘Vaccines’ or Gene Therapy Products? – Part 2
When considering a drug for emergency use authorization (EUA), the Food and Drug Administration (FDA) selects an internal advisory committee to review information and data submitted to the FDA by the pharmaceutical company about its new drug. These influential FDA advisory committees, based on that information and data, make recommendations …
Report 95: mRNA COVID-19 Shots – ‘Vaccines’ or Gene Therapy Products? – Part 1
To this day — more than three years after Pfizer and Moderna’s mRNA COVID-19 drugs received Emergency Use Authorization (EUA) — television, radio, and the Internet still inundate the public with ads, messages, and stories about COVID vaccines. But, are the mRNA COVID-19 shots genuinely vaccines? These products never aligned …
Florida Grand Jury Issues First Presentment in Investigation of Potential Criminality During COVID
On December 13, 2022, Florida Governor Ron DeSantis appointed a statewide Grand Jury to investigate whether crimes or wrongdoing were committed against Floridians regarding the COVID-19 vaccine. The information below highlights a lot of the key findings of the Grand Jury in their initial presentment. However, I didn’t go into much …
FOIA – June 2023: FDA Found Seven ‘Objectionable Conditions’ at Pfizer’s Michigan COVID Vaccine Manufacturing Site: Notifies Pfizer.
Most of us assume that pharmaceutical plants produce medications in clean, contamination-free settings and follow clear protocols. That should be the norm. But the FDA issued a Form 483 to Pfizer’s Kalamazoo, Michigan, manufacturing plant on June 16, 2023, revealing seven alarming observations about the conditions there. The plant is …
On the Pathogenesis of Turbo Cancer Induced by COVID-19 mRNA Vaccines: a Hypothesis.
This short memo makes the case that turbo cancers in patients who received mRNA vaccines can be explained by the observed uptake of those vaccines by macrophages and dendritic cells, based on a well-documented but not widely known theory of carcinogenesis. An increasing number of clinical oncologists and pathologists are …
Letter to Texas Attorney General Ken Paxton: Vaccinated Deaths in Pfizer’s COVID Vaccine Clinical Trial Not Disclosed to FDA with EUA Data.
Dr. Jeyanthi Kunadhasan Team 3 DailyClout P.O. Box 24 Millerton, NY 12546 The Honourable Ken Paxton Attorney General of Texas (469) 247-2360 P.O. Box 3476 McKinney, Texas 75070 RE: Undisclosed Deaths in C4591001 Trial at the Vaccine and Related Biological Products Advisory Committee (VRBPAC) on December 10, …
Report 94: Pfizer Secretly Studied a Heart Damage Marker, Troponin I, in Five- to 15-Year-Olds, Following mRNA COVID Vaccination in 2021.
We warned that there was proof that the Pfizer BNT162b2 mRNA COVID vaccine caused heart damage in teens and young adults, as early as May of 2021. As more information surfaces from the court-mandated release of Pfizer clinical trial documents by the FDA, and via FOIA’d emails, the CDC’s cover-up …
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 …
FOIA’d FDA ‘Establishment Inspection Reports’ of Pfizer COVID Vaccine Manufacturing Facilities Reveal “Inadequate Quality Oversight,” Deficient Deviation Investigations, Ignored Standard Operating Procedures, and More.
Amy Kelly, COO of DailyClout.io and Project Director for the WarRoom/DailyClout Pfizer and Moderna Documents Analysis Project, received a partial production of documents in response to her Freedom of Information Act (FOIA) request submitted to the Food and Drug Administration (FDA) for “all FDA inspection reports from inspections of Pfizer …
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 91: FDA Based Moderna’s mRNA COVID Vaccine Approval on Test of a Completely Different Non-COVID Vaccine. Only Males Included in Test.
Moderna researchers did not test their COVID-19 mRNA drug, called SPIKEVAX, to find out where it would go in our bodies (biodistribution). Instead, their biodistribution study was for a completely different vaccine. Despite this substitution of one drug study for another, the U.S. Food and Drug Administration (FDA) approved SPIKEVAX …