by Stefan Stanford, All News Pipeline:
Plenty has been said about the EUA Vaccine document disclosures the CDC, FDA, and Pfizer were forced to make against their will. But not enough. The Vaccine extremists are still shouting about “misinformation.” To their credit, there was a lot of that, but it was mostly on their side.
The latest revelation to be ignored by the “Jab ’em or Bust” coalition comes from Aaron Siri. “[A]fter multiple legal demands, appeals, and two federal lawsuits, the CDC finally capitulated and agreed to a court-ordered schedule compelling it to produce the data.”
The Informed Consent Action Network (ICAN) took the firehose of information and broke it all down. But the data comes with a story.
TRUTH LIVES on at https://sgtreport.tv/
V-safe’s data shows that 7.7% of its approximate 10 million users reported having to receive medical care after receipt of a Covid-19 vaccine, and over 70% of those users sought outpatient/urgent clinical care, emergency room care, and/or were hospitalized.
V-Safe is the app for people who got The Jab. Its purpose was side-effect surveillance, and 10 million Vaxx recipients used it. Aaron explains how the application works here. V-Safe only allowed the user to select from a pre-determined list of known side effects. There were text fields, but those are cumbersome mechanisms, and none of that data has been released. ICAN is still fighting to get it. So we’ve got a CDC surveillance app and 10 million Jabbed app users, so what’s the problem?
First, let’s remind ourselves what was known about potential adverse events before any Covid-19 vaccine was administered to the general public:
– A July 2020 New England Journal of Medicine study titled “An mRNA Vaccine against SARS-Cov-2 – Preliminary Report” highlighted 35 adverse events that were related to the mRNA vaccination, including eye disorders, gastrointestinal disorders, musculoskeletal and connective tissue disorders, and nervous system disorders.
– An October 16, 2020 JAMA article titled “Postapproval Vaccine Safety Surveillance for COVID-19 Vaccines in the US” stated that “AESIs [Adverse Events of Special Interest] are likely to include allergic, inflammatory, and immune-mediated reactions, such as anaphylaxis, Guillain-Barré syndrome, transverse myelitis, myocarditis/pericarditis, vaccine-associated enhanced respiratory disease, and multisystem inflammatory syndrome in children.”
– In a CDC presentation dated October 30, 2020, titled “CDC post-authorization/post-licensure safety monitoring of COVID-19 vaccines,” a preliminary “list of VSD pre-specified outcomes for RCA [rapid cycle analysis]” and “list of VAERS AEs[ adverse events] of special interest” both included acute myocardial infarction, anaphylaxis, convulsions/seizures, encephalitis, Guillain-Barre syndrome, immune thrombocytopenia, MIS-C, myocarditis/pericarditis, and transverse myelitis, among others.
Again, the fact that mRNA can cause these serious conditions was raised before the first Covid-19 vaccine was authorized for use by the general public in December 2020 – in fact, months before.
None of these conditions are listed as checkbox options for app users to select during their reporting, which issued a prompt for updates “…every day for a week after a shot. Users are then prompted to submit a “check-in” every week for six weeks. And then at six months and one year after the shot.”
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