CDC Won’t Admit Hundreds of Safety Concerns Over Vaccines

Based on monitoring results received by The Epoch Times, the Center for Disease Control and Prevention (CDC) has found hundreds of safety alerts for the two most commonly given COVID-19 vaccinations.

Proof That Vaccines Can Be Unsafe

Examination of adverse event data provided to the Vaccine Adverse Event Reporting System revealed signs of Bell’s palsy, blood coagulation, clots, and death, among others.

VAERS (Vaccine Adverse Event Reporting System) is the country’s warning procedure for vaccine concerns, according to the CDC and the Food and Drug Administration (FDA), which operate VAERS.

The major analysis conducted by the CDC evaluated reports of specific adverse reactions after administration of a Moderna or Pfizer COVID-19 vaccine against reports of adverse events. These events would follow the administration of any alternative vaccine or all non-COVID-19 vaccinations.

The analytical type is called Proportional Reporting Ratio (PRR).

Safety signals indicate that a problem may be associated with a vaccine. Signals require additional research to establish a potential connection. The CDC analyzed adverse outcomes reported between December 14, 2020 and July 29, 2022.

The Epoch Times received the findings after the CDC declined to release them to the public via a Freedom of Information Act request.

VAERS is a passive review and reporting process that welcomes reports from anyone. Though the majority are submitted by healthcare workers instructed during the COVID-19 epidemic to report information if post-vaccination complications arose. People who file false reports are subject to fines.

Reports do not establish causality or a connection between an occurrence and a vaccine. Nonetheless, research reveals that the number of reported post-vaccination incidents is frequently an underestimate of the true incidence.

In operational procedure documentation, the CDC and FDA indicated that authorities would monitor VAERS for possible new safety issues for COVID-19 vaccines, with the CDC doing PRR analysis.

The CDC has provided repeated false statements regarding data mining, but eventually admitted the monitoring mechanism was not implemented until 2022, over a year after the Pfizer and Moderna vaccines were approved.

PRR includes comparing the frequency of a given adverse event following the administration of a particular vaccine against the incidence after the delivery of all other vaccines.

As per the CDC, a signal is generated when three criteria are met: a PRR of at least two, a chi-squared value of at least four, and three or more instances of the incident following the receipt of the studied vaccination.

Chi-squared tests are a quantitative method for analyzing data.

Science Has Spoken

The statistics acquired by The Epoch Times indicate that hundreds of adverse reactions (AEs) satisfy the definition, including dangerous diseases such as blood clots in the lungs, excessive menstrual bleeding, a shortage of oxygen to the heart, and sometimes even death.

Experts were alarmed by the high numbers, notably the chi-squared values.