While the F.D.A. approved these vaccines, the Centers for Disease Control and Prevention, an agency within the Department of Health and Human Services, is charged with monitoring the safety of all vaccines, including the COVID-19 vaccines approved by the F.D.A. The C.D.C. claims that these "COVID-19 vaccines are being administered under the most intensive vaccine safety monitoring effort in U.S. history[.]". The federal government has mandated that millions of Americans receive these vaccine products.
As for the pre-licensure data submitted by the pharmaceutical companies, the F.D.A. took the position in another FOIA action that, because it needs to deidentify that data, it needs at least 75 years to produce the data to the public.
The C.D.C. has deployed a new safety monitoring system for the COVID-19 vaccines, v-safe, and the data within v-safe is already available in deidentified form and could be forthwith released to the public.
V-safe is a smartphone app that allows vaccine recipients to "Tell C.D.C. about any side effects after getting the COVID-19 vaccine." The purpose of the app "Is to rapidly characterize the safety profile of COVID-19 vaccines when given outside a clinical trial setting and to detect and evaluate clinically important adverse events and safety issues that might impact policy or regulatory decisions."
Although the C.D.C. has "Access to the individualized survey data," Oracle can only access "Aggregate deidentified data for reporting. Plaintiff asked through its instant FOIA requests that the C.D.C. produce the deidentified data from the v-safe program in the same form that Oracle can access. Plaintiff believes that to assure transparency regarding the government's claim that COVID-19 vaccines are"safe and effective," the public should have immediate access to all v-safe data, in deidentified form, and therefore, once the C.D.C. produces that data, Plaintiff intends to make it publicly available.
Despite the fact that the deidentified data already exists, it is already in the hands of a private company, and the C.D.C. has never objected to its production, the C.D.C. has so far failed to produce it to Plaintiff or to the American public.
It intends to make all v-safe data immediately available to the public so that independent scientists can immediately analyze that data.
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Saturday, January 1, 2022
CDC Joins FDA, Wants To Hide Jab Safety Data From Public Even Though The Taxpayers Paid For It
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