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Pfizer and BioNTech have submitted an application to the U.S. Food and Drug Administration seeking emergency use authorization for another COVID-19 vaccine booster shot for individuals 65-years-old and above, according to a press release .
The course for most people ages 12 and over currently involves three jabs — two shots for the primary series followed by a single booster dose — though Centers for Disease Control and Prevention indicates that immunocompromised individuals ages 12 and older should receive four vaccine doses, comprised of three doses of an mRNA vaccine for their primary series, as well as a single booster shot.
Pfizer CEO Albert Bourla indicated during a recent interview that a fourth shot will be needed.
“Right now the way that we have seen, it is necessary, a fourth boost, right now,” he said. Bourla described the protection provided by a third shot as “quite good for hospitalizations and deaths,” but he said it is “not that good against infections” and “doesn’t last very long.”
When asked whether he thinks people will need to prepare to get an annual booster shot, Bourla said, “I think so.”
Bourla said that they are trying to develop a vaccine that shields people against all variants and […]
Read the whole story at www.theblaze.com
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FDA revokes Emergency Use Authorization for Monoclonal Antibody treatment for Covid-19. Looks like the FDA is pushing for the Pfizer and Merck antiviral pills. This is so wrong. Big pharma essentially writes and directs the policies for federal health agencies. Everything health agencies do benefits pharma. They need to stop all experimental tx and focus on the real treatments like ivermectin and HCQ. There’s no need to make people Guinea pigs when there are proven safe drugs. If you want to get Ivermectin you can visit https://ivmpharmacy.com