Corruption: CDC Knowingly Left Serious Adverse Events Off Post-Vaccination Surveys RELATED: >>/news/19670/ The US Centers for Disease Control and Prevention (CDC) didn’t include serious adverse events like heart inflammation on post-vaccination surveys even though the agency knew the issues could be linked to COVID-19 vaccines, documents show. Even before the surveys were rolled out in December 2020 after the first vaccines were authorized, the CDC knew that myocarditis—a form of heart inflammation since confirmed as being caused by the Pfizer and Moderna shots—and other serious adverse events were of “special interest” when it came to the vaccines, according to a newly disclosed version of the protocol for the survey system. The Nov. 19, 2020, protocol for V-safe, the survey system, lists myocarditis, stroke, death, and a dozen “prespecified medical conditions.” The protocol was obtained by the Informed Consent Action Network (ICAN), a nonprofit that seeks transparency around health information. All of the conditions can cause severe symptoms. V-safe is a system of surveys that was introduced during the COVID-19 pandemic to monitor vaccine safety. It was developed and is managed by the CDC. Updated versions of the protocol list the same 15 adverse events. None of the conditions were included in the actual surveys. Respondents could check boxes if they experienced certain symptoms, but only 10 lower-level problems such as fever and nausea were listed as options. “It’s deeply troubling that the CDC would construct V-safe in a manner that does not permit it to be able to easily assess the rate of harm from adverse events the CDC had already identified as potentially being caused by these products,” Aaron Siri, a lawyer representing ICAN, told The Epoch Times. “This calls into question what the CDC was really trying to accomplish with V-safe. Was it trying to assess the actual safety of these products? Or was it trying to design a system that would be more likely to affirm its previous public pronouncements regarding the safety of these products?” The CDC did not respond to a request for comment for this article. The CDC has resisted releasing the results from the field, insisting that it would be too onerous to review the 6.8 million entries for personally identifiable information (PII), according to a joint status report made to the court in November 2022. The agency declined a request from ICAN to provide a random sample of a few hundred entries, which plaintiffs say would back their argument that the entries likely hold little or no PII such as names and addresses. The entries are important because they would show how many respondents reported experiencing the prespecified adverse events like heart inflammation. https://www.zerohedge.com/markets/cdc-knowingly-left-serious-adverse-events-post-vaccination-surveys-documents-show