Pfizer Vaccine Faces Final Hurdle Before FDA Panel

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LONDON, ENGLAND - DECEMBER 08: Sodium chloride is measured to be added to a phial of the Pfizer/BioNTech COVID-19 vaccine concentrate ready for administration at Guy's Hospital at the start of the largest ever immunisation programme in the UK's history on December 8, 2020 in London, United Kingdom. More than 50 hospitals across England were designated as covid-19 vaccine hubs, the first stage of what will be a lengthy vaccination campaign. NHS staff, over-80s, and care home residents will be among the first to receive the Pfizer/BioNTech vaccine, which recently received emergency approval from the country's health authorities. (Photo by Victoria Jones - Pool / Getty Images)

The Pfizer Covid vaccine could begin shipments this weekend if it receives a favorable review on Thursday from the Food and Drug Administration. A panel of experts is set to give a final review to data on the drug. The AP writes:

The FDA panel functions like a science court that will pick apart the data and debate — in public and live-streamed — whether the shot is safe and effective enough to be cleared for emergency use. The non-government experts specialize in vaccine development, infectious diseases and medical statistics. The FDA is expected to followthe committee’s advice, although it is not required to do so.

A positive review and speedy approval seem likely despite a cautionary note from the U.K. where a warning was delivered for those who have severe allergic reactions not to take the drug.

The meeting of FDA scientists and specialists is also a chance for a little PR.

Notes the AP: The meeting also gives regulators an opportunity to try to boost public confidence in the breakneck development process that has produced the Pfizer-BioNTech vaccine and a string of other upcoming shots in less than a year.