Are We Really Informed?
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    • Introduction
    • From the Author
    • FDA and Pfizer Knew Before Rollout
    • VAERS Data
    • CDC Not Running Key Analysis
    • Cardiac Concerns
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    • Real People Harmed
    • Fertility Concerns and Abnormal Findings
    • Other Notable Studies
    • Funeral Directors/Pathologists Findings
    • Appeal to Local Doctors
    • Prior Experiments on Targeted Populations
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    • Blood/Contaminants in Vials
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    • Plea about Hospital Protocols
    • Call to Action: Childhood Vaccine
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CDC Admits Did Not Run Key Analysis
​of VAERS System  


​Hot off the press:  In a September 2, 2022 letter to Senator Ron Johnson, CDC Director Walensky admits that in 2021 they did not perform the Proportional Reporting Ratio (PRR) on reports submitted to the Vaccine Adverse Event Reporting System even though their “(VAERS) Standard Operating Procedures for COVID-19 (as of 29 January 2021)” states that they would.  
​
According to the SOP (Standard Operating Procedure) document: “CDC will perform Proportional Reporting Ratio (PRR) analysis (see section 2.3.1, p. 14), excluding laboratory results, to identify AEs that are disproportionately reported relative to other AEs.”

Also in the SOP, the “CDC will perform PRR data mining on a weekly basis or as needed. PRRs compare the proportion of a specific AE following a specific vaccine versus the proportion of the same AE following receipt of another vaccine …. A safety signal is defined as a PRR of at least 2, chi-squared statistic of at least 4, and 3 or more cases of the AE following receipt of the specific vaccine of interest”

Walensky’s recent letter to Sen. Johnson stated:  “CDC performed PRR analysis between March 25, 2022, through July 31, 2022” and “CDC also recently addressed a previous statement made to the Epoch Times to clarify PRR were not run between February 26, 2021, to September 30, 2021.”  

Minimally, 7 months of negligence vs. the weekly standard listed in their Operating Procedure 
SOP Full Document:  https://www.documentcloud.org/documents/22119655-cdc-vaers-sop-2021
Letter to Sen. Johnson:   https://www.documentcloud.org/documents/22309653-walensky-letter


IN 9/2/22 LETTER, WALENSKY ALSO STATED: 
“CDC consistently performs extensive data collection and analysis to detect potential adverse events and safety signals and then communicates this information to the public.
For example, VAERS staff conducted assessments showing that causal associations exist between thrombosis with thrombocytopenia syndrome and Janssen’s COVID-19 vaccine and between myocarditis and mRNA COVID-19 vaccination.
”

Was that communicated to patients when receiving their vaccine injections?
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  • Home
  • Segmented Version
    • Introduction
    • From the Author
    • FDA and Pfizer Knew Before Rollout
    • VAERS Data
    • CDC Not Running Key Analysis
    • Cardiac Concerns
    • Mortality & Life Insurance Data
    • Real People Harmed
    • Fertility Concerns and Abnormal Findings
    • Other Notable Studies
    • Funeral Directors/Pathologists Findings
    • Appeal to Local Doctors
    • Prior Experiments on Targeted Populations
    • Spike Protein & LNP Toxicity
    • Immune System Degradation
    • Blood/Contaminants in Vials
    • News Sources
    • New Bivalent Vaccines
    • Where To Get Help If Injured
    • Plea about Hospital Protocols
    • Call to Action: Childhood Vaccine
    • Validate for Yourself
  • Full Document
  • Downloadable/Shareable
  • Contact