Youtube and FDA hide covid19 vaccine problems Why?, Watch Senator Ron Johnson video on vaccine injured and medical experts, FDA fights FOIA request and lawsuit, What did 5 Pfizer test vaccinated die of?
“Because COVID vaccines use experimental technology that may pose serious side effects such as blood clots, Yeadon said, “we should absolutely not be offering them to young, healthy people who are not at risk from the virus.””..Dr. Mike Yeadon, former vice president of Pfizer
” if you let your healthy teen – much less your healthy child – get this vaccine, you are insane.”…Alex Berenson
“So do not be afraid of them, for there is nothing concealed that will not be disclosed, or hidden that will not be made known.”…Matthew 10:26
Every step of the way, from the source of Covid19 in China, clinical trial data, EUA (emergency use authorization) disclosures to the impact of vaccines on innocent humans, we have been lied to and kept in the dark.
The FDA and CDC are clearly complicit.
Recently Youtube took down the video of a roundtable discussion hosted by Senator Ron Johnson of a panel of experts featuring doctors and scientsts who question the Covid Vaccines safety.
“For the fifth time this year, YouTube suspended Sen. Ron Johnson’s (R-Wis.) YouTube channel — this time for “spreading misinformation” in a video of a Nov. 2 roundtable discussion featuring scientists, doctors and people injured by COVID vaccines. Or as Johnson said in a tweet: “For the 5th time this year, @YouTube is censoring me from telling you the truth.”
“
https://childrenshealthdefense.org/defender/youtube-censors-sen-ron-johnson-covid-vaccine-safety/
Watch the video:
The FDA is being sued for fighting and delaying data release for a FOIA request.
FROM ATTORNEY AARON SIRI.
FDA PRODUCES THE FIRST 91+ PAGES OF DOCUMENTS FROM PFIZER’S COVID-19 VACCINE FILE
Two months and one day after it was sued, and close to 3 months since it licensed Pfizer’s Covid-19 vaccine, the FDA released the first round of documents it reviewed before licensing this product. The production consisted of 91 pdf pages, one xpt file, and one txt file. You can download them here.
While it is for the scientists to properly analyze, let me share one observation. One of the documents produced is a Cumulative Analysis of Post-Authorization Adverse Event Reports of [the Vaccine] Received Through 28-Feb-2021, which is a mere 2 ½ months after the vaccine received emergency use authorization (EUA). This document reflects adverse events following vaccination that have completed Pfizer’s “workflow cycle,” both in and outside the U.S., up to February 28, 2021.
Pfizer explains, on page 6, that “Due to the large numbers of spontaneous adverse event reports received for the product, [Pfizer] has prioritised the processing of serious cases…” and that Pfizer “has also taken a [sic] multiple actions to help alleviate the large increase of adverse event reports” including “increasing the number of data entry and case processing colleagues” and “has onboarded approximately [REDACTED] additional fulltime employees (FTEs).” Query why it is proprietary to share how many people Pfizer had to hire to track all of the adverse events being reported shortly after launching its product.
As for the volume of reports, in the 2 ½ months following EUA, Pfizer received a total of 42,086 reports containing 158,893 “events.” Most of these reports were from the U.S. and disproportionately involved women (29,914 vs. 9,182 provided by men) and those between 31 and 50 years old (13,886 vs 21,325 for all other age groups combined, with another 6,876 whose ages were unknown). Also, 25,957 of the events were classified as “Nervous system disorders””
Pfizer lied in their public reports about the number of vaccinated deaths in their clinical trials.
Their were 5 more deaths that were reported to the FDA but the cause of death was not revealed.
Is that one of the reasons the FDA is fighting the release of FOIA data?
“Pfizer somehow miscounted – or publicly misreported, or both – the number of deaths in one of the most important clinical trials in the history of medicine.
And the FDA’s figures paint a notably more worrisome picture of the vaccine than the public July numbers. Though the absolute numbers are small, overall deaths were 24 percent higher among vaccine recipients.
The update also shows that 19 vaccine recipients died between November and March, compared to 13 placebo recipients – a difference of almost 50 percent.
Were the extra deaths cardiac-related? It is impossible to know. The FDA did not report any additional details of the deaths, saying only that none “were considered related to vaccination.””
Read more here:
https://parler.com/profile/Citizenwells/posts
Citizen WElls 