BREAKING: Great news! @Pfizer to submit an Emergency Use Authorization request to @US_FDA *TODAY* for its #coronavirus vaccine—they’ll will distribute the #vaccine "within hours after authorization.”
Pfizer has enough to dose ~12.5 million Americans this year, much more in 2021.
Pfizer has enough to dose ~12.5 million Americans this year, much more in 2021.
Pfizer’s #vaccine was 95% effective at preventing #COVID19 and had NO serious safety issues.
✅94% effective in people >65, who are more likely to develop life-threatening illness
✅Safety data available for 100 children between 12-15 yo
I fully expect FDA to authorize it.😄
✅94% effective in people >65, who are more likely to develop life-threatening illness
✅Safety data available for 100 children between 12-15 yo
I fully expect FDA to authorize it.😄
https://twitter.com/DrDenaGrayson/status/1329047746532290561
Once Pfizer and BioNTech file their application, the data will be scrutinized by regulators — including at a full-day advisory committee meeting in which external scientists will meet to make recommendations to the agency on whether it should clear the vaccine for broader use.🧐
Pfizer’s data include a minimum of a 2-month safety follow up for the LAST person enrolled in the #vaccine trial—longer-term follow up is available for those dosed earlier.
NO serious safety issues were seen. The most severe safety issues were headache or fatigue in <3%.
NO serious safety issues were seen. The most severe safety issues were headache or fatigue in <3%.
https://twitter.com/drdenagrayson/status/1329049758955081728
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