Sourced of - U.S. Food and Drug Administration - https://www.youtube.com/watch?v=BFdzNUus_CE&t=23603s Starting at 6 H 33m Analyzed by : https://tobyrogers.substack.com/p/the-end-of-covid-19-vaccine-safety I. The end of the beginning Yesterday, the FDA’s Vaccines and Related Biological Products Advisory Committee approved a bivalent Covid-19 shot with the Wuhan strain and the Omicron variant. The vote was: 19 yes. 2 no. A few thoughts: The Wuhan strain is no longer in circulation. So they are vaccinating against a strain that no longer exists. The Omicron variant that they are going to put into this shot is Omicron BA.4/BA.5: 1. By the time it gets to market in the fall, Omicron BA.4/BA.5 will likely no longer be in circulation. 2. There is no efficacy data whatsoever on vaccines against Omicron BA.4/5. 3. There is no safety data whatsoever on vaccines against Omicron BA.4/5. 4. They do not intend to gather any efficacy or safety data between now and when these shots will be released in the fall: At the meeting, the manufacturers (Moderna, Pfizer, and Novavax) were asked what their production timelines are… and they said out loud, “So long as we don’t have to provide any clinical data, we’ll have them ready by fall.” No one had a problem with that. Ofer Levy said that he was concerned about the lack of safety data (there is none) and asked if the FDA intended to gather any. FDA vaccine head Peter Marks said that he was “comfortable” that the Sentinel BEST Initiative would catch any safety signals after these shots are introduced into the market. No one has ever heard of Sentinel BEST. Meanwhile Dr. Marks disparaged the Vaccine Adverse Events Reporting System (VAERS) that has shown 29,031 reports of death following Covid-19 shots. So the FDA is going to introduce reformulated shots into the population this autumn with no safety data and then try to spot adverse events in the population after the fact using a safety system no one has ever heard of