20 Sep. 2021 12:22 Uhr
A panel of experts from the US FDA has overwhelmingly rejected an application for approval of Pfizer’s corona booster vaccination, expressing doubts about its safety. During his presentation to the panel, lead coronavirus researcher Steve Kirsch stated that “Pfizer’s vaccine kills more people than it saves”.
A panel of experts from the US Food and Drug Administration (FDA), after more than eight hours of meeting by 16-2 votes, rejected a broader application for approval of booster doses of the Pfizer vaccine for anyone 16 years and older six months after a full vaccination coverage.
The Panel members expressed doubts about the safety of a booster dose in younger adults and adolescents and complained about the lack of data on the safety and long-term effectiveness of a booster dose.
However, the advisory panel unanimously voted to recommend emergency approval of a booster dose of the Pfizer vaccine for people aged 65 and over and those at high risk of developing severe COVID-19 disease six months after the first two vaccinations. Some of the advisors – a group of vaccine experts, immunologists, pediatricians, infectious disease specialists and public health experts – said the process was hasty. Several members asked for more data during the meeting.
“In my opinion it is likely to be beneficial for the elderly and may also be useful for the general population,” said Dr. Ofer Levy, an infectious disease specialist at Boston Children’s Hospital. “I just don’t think the data is that far.”
The administration of US President Joe Biden announced in August that it would make booster vaccinations available from September 20th. This announcement was controversial because it came before the FDA could review Pfizer’s application and allow the U.S. Centers for Disease Control and Prevention’s panel of experts to consider the need for booster vaccinations.
Steve Kirsch, executive director of the COVID-19 Early Treatment Fund, stated during his presentation to the panel that the COVID-19 vaccines are actually killing more people than they are saving. Kirsch emphasized:
“I’m going to focus today on the elephant in the room that nobody likes to talk about: that the vaccines kill more people than they save. We have been led to believe that the vaccines are perfectly safe, but that’s just not true. In the six-month report from Pfizer, for example, had four times as many heart attacks in the treatment group, and it wasn’t just a mishap. The VAERS (Vaccine Adverse Event Reporting System) shows that heart attacks are 71 times more common than after these vaccines other vaccines. “
Kirsch continued his presentation by showing the number of excess post-vaccination deaths that were required to save a life from COVID-19. “Only the Vaccine Adverse Event Reporting System (VAERS) data are statistically significant, but the other numbers are worrying,” said Kirsch. He explained:
“Even if the vaccines offer 100 percent protection, it still means we kill two people to save a life.”
“Four experts conducted analyzes based on completely different non-US data sources, and they all found roughly the same number of vaccination-related deaths, 411 deaths per million doses. That means 115,000 people ( due to the COVID-19 vaccines), “Kirsch continued.
Kirsch then pointed to the, in his opinion, very worrying data, which came from Israel. The researcher stated:
“The real numbers confirm that we are killing more people than we are saving. And I would like to look at the data from the Israeli Ministry of Health on those over 90, where we went from a vaccination rate of 94.4 percent in the past four months 82.9 percent have fallen. In the most optimistic case, this means that 50 percent of the vaccinated and 0 percent of the unvaccinated have died. Until you can explain this to the public, you cannot approve the booster vaccinations. “
While the FDA is not required to follow the panel’s recommendations, it usually does so, so the agency will likely extend its approval of Pfizer’s vaccine to booster vaccinations for those most susceptible to the virus. FDA approval would only apply to Pfizer. The vaccines manufactured by Moderna and Johnson & Johnson must be tested separately.
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