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MSNBC Andrea Mitchell Reports July 11, 2024

Contact tracing is largely gone. I think and i believe that we should be treating every case as if its a variant during this pandemic right now. The good news according to dr. Anthony fauci is Johnson Johnsons new singledose vaccine could help get more people vaccinated and prevent severe disease and hospitalizations as the virus continues to mutate and replicate. We have now a valueadded additional vaccine candidate. This is a singleshot vaccine in which you start to see efficacy anywhere from 7 to 10 days. It is inexpensive and the company is capable of making doses in the numbers of billions. Joining me now nbc news chief White House Correspondent and Weekend Today cohost Kristen Welker. Dr. Celine gounder, a member of bidens
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MSNBC MTP Daily February 11, 2022 18:34:00

They voted for emergency use authorization, then the cdc would take a look at this. the cdc had said that it was possible if everything went well to have shots in arms by president s day. earlier this week pfizer s ceo seemed confident that the fda would take a look at this and authorize this. as you mentioned just yesterday president biden told lester we were on the verge of this as well. so this is a significant change. so why, you know, what s the significance here in terms of why didn t they wait until submitting this emergency use authorization application when it had more complete data? you ll remember there was a lot of pressure to get this vaccine to the youngest children. in december late last year, pfizer said that two doses did not provide a significant enough immune response but it didn t have the data for the third dose. now these are smaller doses than ....

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MSNBC MTP Daily February 11, 2022 18:33:00

To help us break down this news, i m also joined by dr. irwin redletter. thanks to all of you for being here. gabe, set the table. break down this news for us. why is pfizer pulling their fda application? millions of parents who were waiting on this, they re going to have to wait a little longer. just within the past few minutes the company saying they plan to extend their rolling submission to the fda, essentially pulling the emergency use authorization application because you might remember next week an fda advisory panel was set to meet on tuesday to discuss this. and typically how this played out is the fda advisory panel would discuss it and then if ....

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CNN New Day With John Berman and Brianna Keilar December 9, 2021 13:23:00

You re seeing it at a magnified level. two messages here, the vaccine effectiveness with the two shots was still pretty good. but clearly was waning. and then over time after they got the boosters, that was sort of the end of august, you did see the numbers come down. so you had 90% effectiveness with the two shots and went to 99% with the booster. so, yeah, clearly the boosters made a difference on top of something that was already pretty good with the overall two-shot regiment. israel for folks aged 12 and up. when are we expecting that here in the u.s.? this is a common question. so we doo no know there was an emergency authorization put in. what is interesting is we heard from the fda, they said typically there is an advisory committee that meets. we have seen a bunch of those. they make a recommendation to the fda. what they said, with this particular emergency use ....

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Merck Seeks FDA Authorization for Antiviral COVID-19 Pill

"The extraordinary impact of this pandemic demands that we move with unprecedented urgency, and that is what our teams have done by submitting this application for molnupiravir to the FDA." ....

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