AutoImmune – MicroReport 11
Main Findings Adverse Events were reported to Pfizer during a 90-day period, following the December 1, 2020, public rollout of its COVID-19 experimental “vaccine” product. In the Pfizer 5.3.6 document, these AEs were categorized by System Organ Classes (SOC), in other words, by systems in the body. Of those whose …
Anaphylaxis – MicroReport 10
Main Findings Adverse Events were reported to Pfizer during a 90-day period, following the December 1, 2020, public rollout of its COVID-19 experimental “vaccine” product. In the Pfizer 5.3.6 document, these AEs were categorized by System Organ Classes (SOC), in other words, by systems in the body. Of those with …
Renal – MicroReport 9
Main Findings Adverse Events were reported to Pfizer during a 90-day period, following the December 1, 2020, public rollout of its COVID-19 experimental “vaccine” product. In the Pfizer 5.3.6 document, these AEs were categorized by System Organ Classes (SOC), in other words, by systems in the body. Of the 69 …
Facial Parsalysis – MicroReport 8
Main Findings Adverse Events were reported to Pfizer during a 90-day period, following the December 1, 2020, public rollout of its COVID-19 experimental “vaccine” product. In the Pfizer 5.3.6 document, these AEs were categorized by System Organ Classes (SOC), in other words, by systems in the body. The demographics of …
Neurological – MicroReport 7
Main Finding Of the 542 neurological adverse events, 95% were defined as serious. 16 were fatal. Adverse Events were reported to Pfizer during a 90-day period, following the December 1, 2020, public rollout of its COVID-19 experimental “vaccine” product. In the Pfizer 5.3.6 document, these AEs were categorized by System …
Pediatrics – MicroReport 6
Main Finding Infants and children under 12 were injected with the Pfizer “vaccine” seven months before the product was approved for children. The 5.3.6 document was compiled by Pfizer for the purpose of reporting adverse events to the FDA. The reporting period was during the first 90 days, starting December …
Cardiovascular – MicroReport 5
ABBREVIATIONS: 5.3.6: Pfizer source document SOC: System Organ Class AE: Adverse Event AESI: Adverse Event of Special Interest EUA: Emergency Use Authorization by FDA PM: Post-Marketing BNT162b2: Pfizer’s mRNA COVID-19 vaccine SEQUELAE: an abnormal condition resulting from a previous disease, injury, or other trauma AGE GROUPS defined in 5.3.6 (p. …
Hepatic – MicroReport 4
ABBREVIATIONS: 5.3.6: Pfizer source document SOC: System Organ Class AE: Adverse Event AESI: Adverse Event of Special Interest EUA: Emergency Use Authorization by FDA PM: Post-Marketing BNT162b2: Pfizer’s mRNA COVID-19 vaccine SEQUELAE: an abnormal condition resulting from a previous disease, injury, or other trauma AGE GROUPS defined in 5.3.6 (p. …
Stroke – MicroReport 2
ABBREVIATIONS: 5.3.6: Pfizer source document SOC: System Organ Class AE: Adverse Event AESI: Adverse Event of Special Interest EUA: Emergency Use Authorization by FDA PM: Post-Marketing BNT162b2: Pfizer’s mRNA COVID-19 vaccine SEQUELAE: an abnormal condition resulting from a previous disease, injury, or other trauma AGE GROUPS defined in 5.3.6 (p. …
Thromboembolic Events – MicroReport 3
5.3.6 Cumulative Analysis of Post-authorization Adverse Event Reports Table 7. AESIs Evaluation for BNT162b2 AESIs Category (Primary Path) OR Respiratory failures (excl neonatal) (HLT) (Primary Path) OR Viral lower respiratory tract infections (HLT) (Primary Path) OR PTs: Acute respiratory distress syndrome; Endotracheal intubation; Hypoxia; Pulmonary haemorrhage; Respiratory disorder; Severe acute …
The Increasingly Inconvenient Number of Nazis
Without the slightest hint of irony, I am beginning to miss the days when the left called everyone on the right a Nazi and was usually wrong. The accusation was almost always lazy, insulting, and routinely aimed at people whose supposedly fascist ambitions amounted to wanting a more secure border. …
Report 101 – Gain-of-Function Research and Origin of SARS-CoV-2, the Virus That Causes COVID-19
After years of half-truths and outright falsehoods, facts are emerging about SARS-CoV-2’s origins. The Wuhan Institute of Virology (WIV) purged important genome sequence information from its servers and was not forthcoming regarding their research, so complete details will never be known. Enough can be pieced together for objective molecular geneticists …
Report 99: How the CDC Hides COVID Vaccine Deaths and Injuries
Albert Benavides has diligently documented techniques used by public health agencies to hide data in their databases. He has exposed the techniques of throttling, time displacement, and removal of all or parts of reports. Mr. Benavides posts frequently on Substack. This report will examine two cases drawn from Vaccine Adverse …
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 …
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 …
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 …
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 …
Report 84 – War Room/DailyClout Research Team Breaks Huge Story: More Cardiovascular Deaths in Vaxxed Than Unvaxxed; Pfizer Did Not Report Adverse Event Signal; Death Reporting Delays Favored Pfizer/Vaccinated
War Room/DailyClout Pfizer Documents Analysis team members Corinne Michels, PhD; Daniel Perrier, Jeyanthi Kunadhasan, MD; Ed Clark, MSE; Joseph Gehrett, MD; Barbara Gehrett, MD; Kim Kwiatek, MD; Sarah Adams , Robert Chandler, MD; Leah Stagno, Tony Damian , Erika Delph, and Chris Flowers, MD have published a bombshell study titled, …