Pfizer Documents Analysis
Report 69 – Pfizer and FDA Knew in Early 2021 That Pfizer mRNA COVID “Vaccine” Caused Dire Fetal and Infant Risks, Including Death. They Began an Aggressive Campaign to Vaccinate Pregnant Women Anyway.
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.”(https://www.phmpt.org/wp-content/uploads/2023/04/125742_S2_M1_pllr-cumulative-review.pdf)The data in the Cumulative Review span “. . . from the time of drug product development to 28-FEB-2021.” …
Report 70 – Histopathology Series Part 4c—Autoimmunity: A Principal Pathological Mechanism of COVD-19 Gene Therapy Harm (CoVax Diseases) and a Central Flaw in the LNP/mRNA Platform
Introduction A new class of illness, termed within this report as CoVax Disease, is now warranted. CoVax Disease encompasses multiple pathological mechanisms of which autoimmunity occupies a central position. In this report, the reader will learn that autoimmunity cases reported to the Vaccine Adverse Events Reporting System in the U.S. …
Internal Report 17: “Musculoskeletal Adverse Events of Special Interest Afflicted 8.5% of Patients in Pfizer’s Post-Marketing Data Set, Including Four Children and One Infant. Women Affected at a Ratio of Almost 4:1 Over Men.”
The WarRoom/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1)—Barbara Gehrett, MD; Joseph Gehrett, MD; Chris Flowers, MD; and Loree Britt—wrote a review of musculoskeletal adverse events of special interest (AESIs) found 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., …
Internal Report 18: “‘Other AESIs’ Included MERS, Multiple Organ Dysfunction Syndrome (MODS), Herpes Infections, and 96 DEATHS. 15 Patients Were Under Age 12, Including Six Infants.”
The WarRoom/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1)—Joseph Gehrett, MD; Barbara Gehrett, MD; Chris Flowers, MD; and Loree Britt—wrote a report about Other Adverse Events of Special Interest (AESIs) found 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., …
Report 73: “Pfizer Knew by November 2020 That Its mRNA COVID Vaccine Was Neither Safe Nor Effective. Here Is What Pfizer’s Employees and Contractors Knew and When They Knew It.”
Introduction Through the review of two documents—Pharmacovigilance Plan for Biologic License Application #125742 Of Covid-19 mRNA vaccine (nucleoside modified) (BNT162b2, PF-07302048) and 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162b2) Received Through 28-Feb-2021—referred to below as “PV” and “5.3.6,” the contributors to this report came to understand …
Report 48: “VAERS – 76% of Vaccine-Related Miscarriages from the Past 30 Years Occurred Once Pregnant Women Started Receiving COVID-19 Vaccines”
If you are pregnant, you are more likely to lose your baby in a miscarriage if you receive a COVID-19 vaccine than if you receive measles, mumps, flu, tetanus, or any other vaccine. This and other alarming facts about risks to babies of vaccinated mothers comes from the U.S. government’s …
Report 46: “How Many Pregnant American Women Received mRNA COVID-19 Vaccines in 2021? Only Estimates Are Available.”
Prospective studies of pregnant women who received lipid nanoparticle plus messenger ribonucleic acid (LNP/mRNA) injections for prevention of COVID-19 during 2021 were scant, leading to difficulty in computing rates of spontaneous abortion, stillbirth, congenital anomaly, perinatal fatality, prematurity and small gestational size. The Centers for Disease Control and Prevention (CDC) …
Report 43: “Failure of Serialization by Pfizer Flouted Established Pharma Rules”
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 protocols …
Report 45: “Is mRNA-LNP Vaccine-Induced Immunity Inheritable? A Preprint Study Shows It Is.”
Some traits acquired via the mRNA-LNP injections are passed genetically from parents to their offspring. The implications of this new finding are profound. Because of this inheritability, mRNA gene therapies – including mRNA “vaccines” – must be prohibited, at least until more is known, for expecting mothers as well as …
Report 42: “Pfizer’s EUA Granted Based on Fewer Than 0.4% of Clinical Trial Participants. FDA Ignored Disqualifying Protocol Deviations to Grant EUA.”
So much has been written about the pivotal Pfizer Trial for COVID-19 (C4591001), that it is sometimes hard to remember that the ‘primary evaluable efficacy’ analysis [Follman DA, 2007) Follmann, D.A. (2007). Primary Efficacy Endpoint. Wiley Encyclopedia of Clinical Trials. https://onlinelibrary.wiley.com/doi/10.1002/9780471462422.eoct341], was granted on the results of 170 subjects out …
Report 41: “2021 CDC and FDA Misinformation – Retroactive Editing, Erroneous Spontaneous Abortion Rate Calculation, Obfuscation in the New England Journal of Medicine”
The following article is a follow-up to Dr. Chandler’s report, “Data Do Not Support Safety of mRNA COVID Vaccination for Pregnant Women,” [https://dailyclout.io/data-do-not-support-safety-of-mrna-covid-vaccination-for-pregnant-women/] which reviewed “Preliminary Findings of mRNA Covid-19 Vaccine Safety in Pregnant Persons,” New England Journal of Medicine, April 21, 2021, and June 17, 2021. To best understand …
Report 40: “Data Do Not Support Safety of mRNA COVID Vaccination for Pregnant Women”
Commentary on Preliminary Findings of “mRNA Covid Vaccine Safety in Pregnant Persons” as Reported by the Centers for Disease Control and Prevention and the Food and Drug Administration, June 17, 2021, New England Journal of Medicine. Currently, the Centers for Disease Control and Prevention (CDC), Advisory Committee on Immunization Practices …
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, …
Report 20: “What Did Pfizer Know, and When Did They Know It? Neurological Harms Concealed.”
This report assists in answering, “What did Pfizer know, and when did they know it?” concerning its COVID-19 vaccine. The report focuses on neurological complaints post-injection with the Pfizer COVID-19 vaccine, as well as on several other, non-neurological reported symptoms. The information presented comes from the Centers for Disease Control …
Report 9: ”Even Big Pharma CEOs recognized that not everyone could be vaccinated – so why Vaccine Mandates?”
Recently, Project Veritas revealed that the CEO of AstraZeneca, Pascal Soriot, told his company in a Zoom call in Dec 2020 that not everyone could be vaccinated; Soriot identified the immune-compromised and people with multiple sclerosis as examples if those who should not be vaccinated with mRNA vaccines. He raised …
Report 8: “Why Was the Pfizer COVID-19 Vaccine Recommended for Use in and Administered to Children When It Was Not Tested in That Age Group?”
Thanks to a court-ordered release of confidential Pfizer documents we have learned that 21 groups of individuals were excluded from phase 1, 2 and 3 of their human trials. Children under the age of 18 were one of these excluded groups. https://www.phmpt.org/wp-content/uploads/2022/04/125742_S1_M5_5351_c4591001-fa-interim-sam-ple-crf.pdf (Annotated Study Book for Study Design: C4591001 Study …
Report 6: “Safe and Effective? We Beg to Differ. Red Flags in the Pfizer Internal Documents.”
Pfizer released the documents on their early efficacy and safety trials of their vaccine. (Pfizer 2.7.3 SUMMARY OF CLINICAL EFFICACY). https://phmpt.org/wp-content/uploads/2021/12/STN-125742_0_0-Section-2.7.3-Summary-of-Clinical-Efficacy.pdf. The results of these documents are used to justify the claim the vaccines are safe and effective. Examine the document! It is evident beyond any doubt. Pfizer lied and …