Pfizer Documents Analysis
Report 79 – mRNA COVID Vaccine-Induced Myocarditis at One Year Post-Injection: Spike Protein, Inflammation Still Present in Heart Tissue.
In spite of widespread censorship, the truth is coming out that myocarditis arising after injection with mRNA COVID “vaccines” is not rare, temporary, or mild. (https://openvaers.com/covid-data/myo-pericarditis) Statement 1: Myocarditis after COVID-19 “vaccine” injection is rare. https://www.cdc.gov/coronavirus/2019-ncov/vaccines/safety/myocarditis.html) [IMAGE 1 — ORIGINAL SOURCE PAGE 290] The Centers for Disease Control and Prevention’s …
Internal Report 22: “Thirty-Two Percent of Pfizer’s Post-Marketing Respiratory Adverse Event Patients Died, Yet Pfizer Found No New Safety Signals.”
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 compelling analysis of Respiratory 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 …
Internal Report 21: “Women Suffered 94% of Dermatological Adverse Events Reported in First 90 Days of Pfizer COVID “Vaccine” Rollout. 80% of These Adverse Events Were Categorized As ‘Serious.’”
The WarRoom/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1)—Barbara Gehrett, MD; Joseph Gehrett, MD; Chris Flowers, MD; and Loree Britt—produced a report about Dermatological 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 1: “Liver Adverse Events—Five Deaths Within 20 Days of Pfizer’s mRNA COVID Injection. 50% of Adverse Events Occurred Within Three Days.”
The WarRoom/DailyClout Pfizer Analysis Post-Marketing Group—Team 1 created the following Liver (i.e., Hepatic) System Organ Class (SOC) Review from data 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., “5.3.6”). (https://www.phmpt.org/wp-content/uploads/2022/04/reissue_5.3.6-postmarketing-experience.pdf) There were 70 patient cases with 94 adverse events reported …
Report 52: “Nine Months Post-COVID mRNA ‘Vaccine’ Rollout, Substantial Birth Rate Drops in 13 European Countries, England/Wales, Australia, and Taiwan.”
Robert W. Chandler, MD, completed extensive research to write the article below. Some of the highlights of this important piece include: Nine months following the rollout of the COVID-19 mRNA “vaccines,” substantial birth rate drops were seen in 13 of 19 European countries, England and Wales (one entity based on …
Internal Report 3: “77% of Cardiovascular Adverse Events from Pfizer’s mRNA COVID Shot Occurred in Women, as Well as in People Under Age 65. Two Minors Suffered Cardiac Events.”
The WarRoom/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1) produced a shocking review of the Cardiovascular System Organ Class (SOC) from data 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., “5.3.6 ”). (https://www.phmpt.org/wp-content/uploads/2022/04/reissue_5.3.6-post-marketing-experience.pdf) 1,403 patients, or 3.3% of the …
Internal Report 4: “Infants and Children Under 12 Given the Pfizer mRNA COVID ‘Vaccine’ Seven Months BEFORE Pediatric Approval. 71% of Adverse Event Cases Classified as Serious.”
The WarRoom/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1)—Barbara Gehrett, MD; Joseph Gehrett, MD; Chris Flowers, MD; and Loree Britt—produced a shocking review of the pediatric data 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., “5.3.6“). (https://www.phmpt.org/wp-content/uploads/2022/04/reissue_5.3.6-postmarketing-experience.pdf) It …
Report 58 – “Autopsies Reveal Medical Atrocities of Genetic Therapies Being Used Against a Respiratory Virus”
Summary Dr. Arne Burkhardt is one of eight international pathologists, physicians, and scientists who were asked to perform a second autopsy, requested by friends and family of the deceased who were not satisfied with the results of the first autopsy. Thirty autopsies and three biopsies were evaluated; 15 cases with …
Internal Report 6: “542 Neurological Adverse Events, 95% Serious, in First 90 Days of Pfizer mRNA Vaccine Rollout. 16 Deaths. Females Suffered AEs More Than Twice As Often As Males.”
The WarRoom/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1)—Barbara Gehrett, MD; Joseph Gehrett, MD; Chris Flowers, MD; and Loree Britt—produced an alarming review of the neurological System Organ Class (SOC) adverse events found in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received Through …
Internal Report 7: “Part 2—‘Autopsies Reveal Medical Atrocities of Genetic Therapies Being Used Against a Respiratory Virus’”
Histopathological reevaluation of serious adverse events and deaths following COVID-19 vaccination Professor Arne Burkhardt Pathologist Reutlingen, Germany Professor Dr. Arne Burkhardt gave an update on his series of autopsy and biopsy cases associated with Spike associated gene therapy entitled “Histopathological reevaluation of serious adverse events and deaths following COVID-19 vaccination” …
Internal Report 8: “The Flawed Trial of Pfizer’s mRNA ‘Vaccine’”
The clinical trial of Pfizer’s mRNA “vaccine” did not prove the mRNA injection is safe and effective, despite Pfizer’s claims to the contrary. In fact, Pfizer stopped collecting useful data long before the planned end date of the clinical trial. Based on an inaccurate diagnostic test confirming COVID-19 in a …
Internal Report 9: “449 Patients Suffer Bell’s Palsy Following Pfizer mRNA COVID Vaccination in Initial Three Months of Rollout. A One-Year-Old Endured Bell’s Palsy After Unauthorized Injection.”
The WarRoom/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1)—Joseph Gehrett, MD; Barbara Gehrett, MD; Chris Flowers, MD; and Loree Britt—produced a disturbing review of the Facial Paralysis System Organ Class (SOC) adverse events found in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received …
Report 61: “Ute Krüger, MD, Breast Cancer Specialist, Reveals Increase in Cancers and Occurrences of ‘Turbo Cancers’ Following Genetic Therapy ‘Vaccines.’”
Ute Krüger, MD, DMedSci (https://lakaruppropet.se/international-conference-pandemic-strategies/) Ute Krüger, MD, DMedSci, is a pathologist educated in Germany now living and working in Sweden. She wrote her doctoral thesis at the Humboldt University in Berlin on the analysis of 7,500 autopsy protocols. With over 25 years of experience in Clinical Pathology and a …
Internal Report 11: “Acute Kidney Injury and Acute Renal Failure Following Pfizer mRNA COVID Vaccination. 33% of Patients Died. Pfizer Concludes, ‘No New Safety Issue.’”
The WarRoom/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1)—Joseph Gehrett, MD; Barbara Gehrett, MD; Chris Flowers, MD; and Loree Britt—produced an alarming review of the Renal (Kidney) System Organ Class (SOC) adverse events found in Pfizer document 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) Received …
Internal Report 12: “In the First Three Months of Pfizer’s mRNA ‘Vaccine’ Rollout, Nine Patients Died of Anaphylaxis. 79% of Anaphylaxis Adverse Events Were Rated as ‘Serious.’”
The WarRoom/DailyClout Pfizer Documents Analysis Project Post-Marketing Group (Team 1)—Joseph Gehrett, MD; Barbara Gehrett, MD; Chris Flowers, MD; and Loree Britt—produced a shocking review of anaphylaxis (severe allergy reaction) adverse events 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 13: “1,077 Immune-Mediated/Autoimmune Adverse Events in First 90 Days of Pfizer mRNA “Vaccine” Rollout, Including 12 Fatalities. Pfizer Undercounted This Category of Adverse Events by 270 Occurrences.”
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 an important review of immune-mediated/autoimmune adverse events 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., “5.3.6“). (https://www.phmpt.org/wp-content/uploads/2022/04/reissue_5.3.6-postmarketing-experience.pdf) This …
Internal Report 14: “34 Blood Vessel Inflammation, Vasculitis, Adverse Events Occurred in First 90 Days After Pfizer mRNA “Vaccine” Rollout, Including One Fatality. Half Had Onset Within Three Days of Injection. 81% of Sufferers Were Women.”
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 an important review of vasculitis adverse events 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., “5.3.6“). The search …
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., …