Dr. Jeyanthi Kunadhasan, WarRoom/DailyClout Researcher, Follows Up with the Therapeutic Goods Administration Re-Emphasizing That Pfizer Had More Vaccinated Deaths Than Placebo Deaths in Its COVID Vaccine Clinical Trial
Following up on her unanswered April 6, 2024, letter to Professor Tony Lawler, Deputy Secretary of Australia’s Therapeutic Goods Administration (TGA), Dr. Jeyanthi Kunadhasan, an anaesthetist and perioperative physician in Australia and Treasurer of the Australian Medical Professionals’ Society, wrote to him again on May 17, 2024. She again expressed …
“Pfizer/FDA Knew in Early 2021 That Pfizer mRNA Injection Caused Dire Fetal and Infant Risks”
Amy Kelly, DailyClout’s COO and Project Director for the War Room/DailyClout Pfizer and Moderna Documents Analysis Project, explains the key findings in Report 69, a bombshell report showing that Pfizer and the FDA knew in early 2021 that the Pfizer mRNA COVID “vaccine” caused dire fetal and infant risks, including death. …
“Effects of N1-Methyl-Pseudouridine in the Pfizer mRNA Vaccine”
Amy Kelly is the COO of DailyClout and Project Director for the War Room/DailyClout Pfizer and Moderna Documents Analysis Project. On DailyClout show Unstoppable, Kelly makes history as she dives into the Pfizer and Moderna reports, bombshell findings, and COVID-19 updates from around the world. In this premier episode, Kelly …
Outspoken: “Amy Kelly/ DailyClout Reveal Canadian Reproductive Damage Crisis Post-2021”
Amy Kelly, DailyClout’s COO and the Director of the WarRoom/DailyClout Pfizer Documents Analysis Project, reveals a stunning analysis she completed of six million individual records belonging to Ontario citizens. The dataset is from the Canadian government, FOIA’d by two Canadian citizens; it represents medical billing codes from the socialized medical …
Canadian Gov’t Database Reveals Catastrophic Reproductive Damage to Men and Women Post-mRNA Vaccine Rollout
Overview We are providing an even more granular analysis of years 2015 through 2022, using data from Ontario Health Insurance Plan (OHIP). This OHIP dataset includes about six million unique patients. Importantly, it contains four years of ‘baseline’ data from before COVID-19 or COVID-19 vaccines appeared in Canada, as well …
Exclusive: Canadian Gov’t Database Reveals Catastrophic Reproductive Damage to Men and Women
Overview An analysis of January 2015 through December 2022 data extracts from the Ontario Health Insurance Plan (OHIP) database exposes a myriad of reproduction-related harms to Ontarians following the rollout of COVID-19 vaccines in Canada. This dataset includes about six million unique patients. Importantly, it contains four years of ‘baseline’ …
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 …