The Great Covid Vax Booster Controversy By Brian Simpson
The U.S. Food and Drug Administration’s (FDA) advisory committee on September 17 overwhelmingly rejected a proposal to distribute booster shots of Pfizer and Covid vaccine to the general public. However, that has not stopped lobbying for the boosters to be delivered, and the word on the street is that it is only a matter of time, because what Big Pharma wants, Big Pharma gets. National Institutes of Health (NIH) Director Dr. Francis Collins believes that COVID booster shots will be recommended for Americans in the upcoming weeks. This too will be the pattern for Australia, where even getting one, or two jabs will still mean that without endless booster shots, one remains “unvaccinated.” Covid is forever.
“National Institutes of Health (NIH) Director Dr. Francis Collins said he would be “surprised” if COVID booster shots were not recommended for other Americans in the upcoming weeks even after the U.S. Food and Drug Administration’s (FDA) advisory committee on Sept. 17 overwhelmingly rejected a proposal to distribute booster shots of Pfizer and BioNTech’s COVID vaccine to the general public.
The FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) recommended the agency approve Pfizer’s application for boosters only for people 65 and older and certain high-risk populations.
In a conversation with “Fox News Sunday,” Collins dismissed the FDA’s decision as being subject to change upon further review of the science.
“I think the big news is that they did approve the initiation of boosters,” Collins said, for older and at-risk Americans. “Remember, they’re taking a snapshot of right now, we’re going to see what happens in the coming weeks.”
Collins said it would surprise him if it does not become clear over the next few weeks that the administration of boosters may need to be expanded. “Based on the data we’ve already seen both in the U.S. and in Israel, it’s clear that the waning effectiveness of those vaccines is a reality and we need to respond to it,” Collins said.
Collins said he was not sure whether boosters will be recommended for all — pointing to concerns of risks outweighing benefits for younger people — but he maintained that boosters for people under 65 will be approved.
Two FDA officials and a group of other leading scientists recently asserted that available evidence does not yet support encouraging COVID booster shots for all Americans.
Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases and chief medical advisor to President Biden, said the FDA’s final decision on making booster shots available is expected later this week. The Centers for Disease Control and Prevention’s (CDC) Advisory Committee on Immunization Practices is separately expected to weigh in on Pfizer’s booster request.
Fauci on Sunday told ABC’s “This Week” that Biden planned to have booster shots ready as soon as this week, pending FDA approval, because “we wanted to be ready.”
“These are the kind of things that when you make a decision, you don’t snap your finger and it gets rolled out the next day,” Fauci said. “When the FDA makes their final determination and very soon thereafter this coming week, you’re going to see the Advisory Committee on Immunization Practices that advises the CDC to perhaps even fine-tune that, so it can be implemented expeditiously.”
Fauci said FDA decisions on booster shots for people vaccinated with Moderna’s or Johnson & Johnson’s vaccines are a few weeks away.
‘COVID Vaccines harm more people than they save,’ physicians tell FDA
During Friday’s meeting, VRBPAC unexpectedly voted against approving boosters for the general population based on a lack of long-term data and stating the risks did not outweigh the benefits.
During the public comment session, numerous experts said data supporting Pfizer’s request for booster doses was inadequate, and several highlighted concerning patterns with data from the CDC’s Vaccine Adverse Event Reporting System or VAERS — requesting more attention be given to potential signals and reported adverse events.
Dr. Jessica Rose, a viral immunologist and virologist stated she “took it upon herself to become a VAERS analyst who organizes data into comprehensive figures to convey information to the public in both published work and video medium.”
Rose said “safety and efficacy are the cornerstones of the development and administration of biological products meant for human use.” She provided a data bridge showing the probability of an adverse event occurring and the severity of the resulting harm to health of individuals in the design population.
“This is a barsoft that shows the past 10 years of VAERS data plotted against the total number of adverse event reports for all vaccines for the years 2011 to 2020 and for COVID associated products — only for 2021,” Rose said.
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