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 […]
“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 […]
Vaccine mandates to stay in Victoria
Summary: “Health workers treating Victoria’s sickest and most vulnerable people will still need their COVID-19 jabs when the state’s pandemic declaration ends. Victoria’s pandemic declaration is due to expire on Wednesday, [October 14, 2022], rendering the few remaining COVID-19 orders and vaccine mandates unenforceable under the legal framework. However, Victorian […]
Report 39: Despite Incomplete Safety Trials, the Food and Drug Administration (FDA) Grants Full Approval to Pfizer-BioNTech’s COMIRNATY® for Adolescents 12-15 Years of Age
Without a completed safety study or expert committee review, the FDA issued a supplemental Biologics License Application (“sBLA”) approval letter granting full FDA approval to Pfizer-BioNTech’s COMIRNATY® COVID-19 mRNA vaccine for use in children ages 12-15. This was done even though safety study completion, on which approval should be based, […]
The Food and Drug Administration (FDA) Grants Full Approval to Pfizer-BioNTech’s COMIRNATY for Adolescents 12-15 Years of Age Despite Incomplete Safety Trials
Without having assembled an expert committee, the FDA issued a supplemental BLA (“sBLA”) approval letter granting full FDA approval to Pfizer-BioNTech’s COMIRNATY COVID-19 mRNA vaccine for use in children ages 12-15. They did this despite the fact that the safety study on which approval should be based will not be […]
Report 32: If Pfizer Controlled the ‘Data’ They Controlled the Outcome
If Pfizer Controlled the ‘Data’ They Controlled the Outcome This Report was written exclusively for DailyClout by the Members of the Pfizer Analysis team. It should not be copied or republished without permission from DailyClout or a full credit and link to DailyClout.io Those in Control of the ‘Data’ Control […]
Moderna Vaccine is Likely More Dangerous Than the Pfizer BioNTech
Moderna Vaccine is Likely More Dangerous Than the Pfizer BioNTech Dear DailyClout, Here is a major study out of France that shows an adverse reaction for myocarditis and pericarditis based on dose effect. The Moderna mRNA vaccine had an odds ratio (a measurement of likely to cause injury) 3.7X greater […]
Pfizer Vaccine Dangers for Pregnant Women – A Letter to Massachusetts Attorney General
Pfizer Vaccine Dangers for Pregnant Women – A Letter to Massachusetts Attorney General June 9, 2022 Attorney General Maura Healey Office of the Attorney General One Ashburton Place 20th Floor Boston, MA 02108 Re: Pfizer-BioNTech experimental mRNA vaccine adverse events for pregnant women Dear Attorney General Healey: […]
GAA Coalition Calls for an End to Vaccine Mandates
In the same week that the FDA just approved a 3rd dose of the Pfizer BioNTech Covid-19 vaccines for the children, without convening the vaccine advisory panel, a significant signal emerged in the fight against the corrupt, censorial government health agencies and their pharmaceutical companies. Free to Fly – Global Aviation Advocacy Coalition Statement […]
Report 07: COVID-19 Vaccines and Pregnancy: Risky Business
COVID-19 Vaccines & Pregnancy: Risky Business This report has been brought to you by DailyClout To date there have not been any human clinical trials conducted by a COVID-19 vaccine pharmaceutical company to determine if vaccines are safe during pregnancy or while breastfeeding. All Emergency Use Authorizations (EUA’s) exclude pregnant […]
A Letter to California Attorney General on Vaccine Adverse Events
May 2, 2022 Attorney General Bonta Office of Attorney General PO Box 944255 Sacramento, CA 94244 DUPLICATE COPY FAXED TO 916-323-5341 RE: California’s Mandatory Covid-19 vaccine and boosters for school children Attorney General: Due to the great public interest, public safety and health issues, and infringement of Constitutional rights posed […]
War Room’s Steve Bannon Praises Dr Naomi Wolf’s Bombshell Pfizer Revelations
War Room’s Steve Bannon praises Dr. Naomi Wolf’s shocking revelations regarding the Pfizer internal documents. These documents are currently being researched by thousands of volunteers in an effort to hold those in power accountable for fraud, misrepresentation, and withholding information on adverse events – information necessary to secure […]
Timeline for China/Pfizer Connections
I’m a member of Team 4. While examining documents, I realized a timeline might be helpful for context and asked Amy if one existed. She suggested I put one together so I’ve been researching various dates having to do with the vaccine development, etc. After listening to your report […]
Report 14: Were We Lied to by the FDA?
What’s the difference between Pfizer’s FDA approved COMIRNATY and the emergency use authorized “vaccine?” Only the law, not science, says the FDA. Were we lied to by the U.S. Food and Drug Administration (FDA) and the media when they told us that, if we received the Pfizer “vaccine” after […]
Report 03: Phase 1 /2 Study of COVID-19 RNA Vaccine BNT162b1 in Adults: Key Processes Missing.
Mulligan, Lyke et al. Nature Published online August 12, 2020. Cite this article as: Mulligan, M. J. et al. Phase 1/2 study of COVID-19 RNA vaccine BNT162b1 in adults. Nature https://doi.org/10.1038/s41586-020-2639-4 (2020). P1 p2: The authors’ put forth the argument that mRNA in BNT162b1 (Note this series used BNT162b1 […]
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