The FDA authorized Covid-19 shots for kids on June 14 and 15 and the “Future Framework” meeting
W3THEMEDIA:
Urgent: on June 28, the ‘Future Framework” will be voted on, and if approved, all reformulated Covid-19 shots will skip clinical trials.
The ‘Future Framework” being voted on June 28th rigs the Covid-19 v@xxine regulatory process by taking the ‘flu strain selection process’ that fails every year and applying it to future (reformulated) C 0vid-19 shots. (See approving FDA member’s emails at the end of this email).
Federal bureaucrats with financial conflicts of interests will then choose which SARS-C oV-2 variants to include in a yearly (or twice yearly)
Covid-19 shot. In the process, all future Covid-19 shots will be deemed automatically ‘safe and effective’ without further clinical trials because they are considered ‘biologically similar’ to existing C ovid-19 shots.”
This the most reckless plan in the history of public health. This is clear proof that the FDA has completely abandoned science and its duty to protect the public.
Vaccines and Related Biological Products Advisory Committee Meeting – 6/28/2022 https://www.youtube.com/watch?v=BFdzNUus_CE
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Below are the email addresses of everyone at the FDA/VRBPAC. Share your own story or copy and paste the message below.
Subject line: All reformulated COVID-19 shots MUST go through proper clinical trials
The safety and efficacy of all reformulated COVID-19 shots must be evaluated through:
Large (50,000+ person) double-blind randomized controlled trials with inert saline placebos conducted by an independent third party. The treatment and control groups must be followed for life to monitor adverse events and all-cause mortality (no more wiping out the control group after 6 months to hide bad outcomes). We also demand greater than 90% efficacy against infection with less than 0.1% Grade 3 or higher adverse events; proper monitoring for carcinogenesis, mutagenesis and impairment of fertility; and immediate release to the public of all clinical trial documents submitted to the FDA.
sean.mccluskie@hhs.gov, commissioner@fda.hhs.gov, DeanofPublicHealth@brown.edu, Aux7@cdc.gov, Peter.Marks@fda.hhs.gov, Hong.Yang@fda.hhs.gov, Richard.Forshee@fda.hhs.gov, Huilee.Wong@fda.hhs.gov, Leslie.Ball@fda.hhs.gov, Doran.Fink@fda.hhs.gov, jerry.weir@fda.hhs.gov, hanae@bcm.edu, paula.annunziato@merck.com, adam.berger@nih.gov, hbernstein@northwell.edu, acohn@cdc.gov, anc0@cdc.gov, hjanes@fredhutch.org, hgans@stanford.edu, david.kim@hhs.gov, asmonto@umich.edu, offit@chop.edu, spergam@fredhutch.org, Jportnoy@cmh.edu, erubin@hsph.harvard.edu, erubin@nejm.org, ashane@emory.edu, swamy002@mc.duke.edu, fullerao@umich.edu, RandyHawkins@cdrewu.edu, officeofthepresident@mmc.edu, JYLee@uams.edu, ofer.levy@childrens.harvard.edu, wayne_marasco@dfci.harvard.edu, cmeissner@tuftsmedicalcenter.org, mrn8d@virginia.edu, stanley-perlman@uiowa.edu, mhsawyer@ucsd.edu, mew2@cdc.gov, jlessler@unc.edu
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