March 30, 2023

FDA Greenlights Pfizer Booster Photos for Elderly, ‘High Risk’ Adults

U. S. officially moves on to next circular of experimental injections

The US Food and Drug Administration has provided its blessing to the utilization of Pfizer’s Covid-19 jab pertaining to booster doses.

The shift could impact millions of Americans, including teachers, grocery workers, and hospital staff.

Heeding advice from the special panel on vaccines, the FDA on Wed moved to approve a third dose of the US drugmaker’s Covid-19 vaccine to be used on seniors as well as  “ individuals 18 through 64 years of age and at high risk of serious Covid-19. ”   It offers also been approved for adults  “ whose frequent institutional or occupational exposure”   to the virus ostensibly places them at a heightened danger of  “ serious problems of Covid-19, including severe Covid-19. ”

The announcement has left lots of room for interpretation, with epidemiologist and senior fellow at the Federation of American Scientists Eric Feigl-Ding  pointing out   that it  “ provides enormous leeway for many people”   to get the vaccine, and  “ not just elderly or even healthcare workers. ”    

Certainly, while the FDA fell short of approving booster shots for the US population as a whole  – a view that has been championed by the administration of US President Joe Biden  – acting FDA Commissioner Janet Woodcock signaled that the athorization could cover large portions of the population due to the character of their work.

“ The FDA amended the EUA for the Pfizer-BioNTech Covid-19 vaccine to allow for a booster dose in certain populations such as healthcare workers, educators and day care staff, grocery store workers and those in homeless shelters or prisons, among others, ”   Woodcock mentioned.

The decision might still come as a dissatisfaction for Biden, who has came back behind the idea that everybody 18 and older should be able to get a booster shot within eight months of their second dosage, promising to start rolling away the revaccination program as soon as September.

The FDA said that its choice was based on  “ scientific evidence, ”   “ currently available data”   on the effectiveness of the vaccine, and on its advisory committee’s recommendations.

Today’s action demonstrates that science and the currently available information continue to guide the FDA’s decision-making for Covid-19 vaccines during this pandemic

Prior to voting in favor of booster shots, the advisory committee reviewed a number of studies submitted by Pfizer that showed the efficacy from the vaccine decreases with time. A single study found that the jab’s efficacy plunged from 93% to 53% against the Delta strain after four several weeks following the second dose.  

Doubts, however , have been raised about the accuracy of Pfizer’s observational studies. Even before the advisory plank backed the proposed booster shots, FDA officials released a document stating that there were  “ known plus unknown biases that can impact [the] reliability”   of the findings. It also noted that available data  “ indicate”   that vaccines  “ still pay for protection against severe Covid-19 disease and death”   in the US.

Alex Jones and Tim Enlow join the display to brief the audience on the rapidly deteriorating scenario on the Texas/Mexico border.

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