An FDA advisory group declined on Friday to recommend that the Pfizer-BioNTech Covid booster shot be approved for people aged 16 and over.
The council voted 16-2 to reject additional doses of an experimental vaccine, citing insufficient data from incomplete clinical studies as well as the risk of heart inflammation, particularly among young males.
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The FDA hearing that preceded the ruling was awe-inspiring. The session lasted eight hours and featured HORRIFIC testimony from American doctors.
On Friday, Dr. Joseph Fraiman, MD, told the FDA that the government does not have data to indicate that the vaccination is more useful to teenage boys than it is hazardous.
Dr. Fraiman told the FDA panel that persons who express vaccine apprehension are not misinformed. “I haven’t seen anything like it… Vaccine skeptics I’ve met in the ER are more informed about vaccine research and their individual COVID risks than doctors are. Many of my nurses, for example, oppose the COVID vaccine despite having seen more COVID fatalities and damage than the majority of people.”
Dr. Fraiman went on to stress that he cannot guarantee that the immunizations are safer for a 30-year-old nurse associate than acquiring the illness.
The Executive Director of the COVID-19 Early Treatment Fund, Steve Kirsch, was the second witness to appear before the FDA. Kirsch argued that immunizations were ineffective.
Steve Kirsch also mentioned that early treatments are more effective than boosters, pointing out that incidences in Israel are at an all-time high, but cases in Uttar Pradesh, India, where Ivermectin is administered, are almost non-existent now.