FDA gave the booster (3d dose) for elementary school children its blessing today.
"On Jan. 3, the FDA authorized the use of a single booster dose of the Pfizer-BioNTech COVID-19 Vaccine for administration to individuals 12 through 15 years of age after completion of primary vaccination with the Pfizer-BioNTech COVID-19 Vaccine. Today’s action expands the use of a single booster dose of the vaccine for administration to individuals 5 through 11 years age at least five months after completion of a primary series of the Pfizer-BioNTech COVID-19 Vaccine. The FDA has authorized the Pfizer-BioNTech COVID-19 Vaccine for use in individuals 5 years of age and older and has approved Comirnaty (COVID-19 Vaccine, mRNA) for use in individuals 16 years of age and older...
The FDA has determined that the known and potential benefits of a single booster dose of the Pfizer-BioNTech COVID-19 Vaccine for children 5 through 11 years of age at least five months after completing a primary series outweigh its known and potential risks and that a booster dose can help provide continued protection against COVID-19 in this and older age groups...
The FDA did not hold a meeting of its Vaccines and Related Biological Products Advisory Committee on today’s action, as the agency previously convened the committee for extensive discussions regarding the use of booster doses of COVID-19 vaccines and, after review of Pfizer’s EUA request, the FDA concluded that the request did not raise questions that would benefit from additional discussion by committee members...”So, after the VRBPAC advisory committee agreed at its last meeting that approving a booster in the fall would require clinical trial data for efficacy since the antibody titers were not reliable, someone higher up than Peter Marks (Director of CBER, the FDA's vaccine division) and Robert Califf (FDA Commissioner) gave the order to forget all that, and find a way to authorize another @!^&*$# dose.
Ignoring both a) its guidance for industry requirements for a COVID authorization, which had been pushed out over and over again over the past 2 years, and b) FDA's recent statements at VRBPAC that actual clinical trial evidence of efficacy would be needed to authorize a booster in the fall, the FDA got the dirty job done, attributing its booster authorization for elementary scchoolchildren to "immunobridging" data and "safety" data in very small numbers of schoolchildren.
The extent of the farce of public health is hard for me to describe and comprehend. All standards have been tossed out, and all authorizations and approvals are now based on the flimsiest of pretenses. They are barely pretending. And to give a useless but dangerous shot to kids is pure evil. Why are they doing it? What is in the shots? Why is this travesty so important? Who is calling the shots? And when will the pitchforks come out?
Yes, incredibly, incomprehensively evil. Even if it is speculation, what is your educated best guess about identifying the puppet masters behind this inhuman travesty?
ReplyDeleteLast year, in March of 2021, the same cast of characters who implemented the 2019 "Event 201" scenario (which, as you may recall, was practically a note-for-note script into covid), implemented yet another table-top exercise based on a scenario of -- wait for it -- an outbreak of monkeypox.
ReplyDeleteThe full write-up of their "simulation" is here:
https://www.nti.org/wp-content/uploads/2021/11/NTI_Paper_BIO-TTX_Final.pdf
On page 10 of their report, in Figure 1, you can see these savvy simulators, in March 2021, predicted the first cases of monkeypox arising on May 15, 2022. Lo and behold, actual cases of monkeypox are now being observed *exactly* as predicted, almost to the very day.
One might read this report as the roadmap for what we can expect to be unfolding next. As though we haven't been through enough hell over the past two years...
Note that, as with the "Event 201" scenario, this exercise was funded/sponsored by the same entity, "Open Philanthropy", the front operation for Dustin Moskowitz (facebook oligarch) and friends. And of course the participants in both exercises include all the usual suspects from Gates Foundation, Wellcome Trust, etc.
Monkeypox -- for fuxx sake! -- all of this would seem so bizarre and laughably unreal. And maybe that's what they are counting on?