The Food and Drug Administration (FDA) is set to implement stricter vaccine approval guidelines after a memo claimed at least 10 children died “after and because of” receiving a COVID-19 shot. The ...
With an FDA accelerated approval in November 2023, Ixchiq became the world’s first shot for chikungunya. Its retreat leaves Bavarian Nordic’s Vimkunya the only available chikungunya vaccine in the U.S ...
Six days after a senior FDA official sent a sweeping internal email claiming that COVID-19 vaccines had caused the deaths of "at least 10 children," 12 former FDA commissioners released an ...
Add Yahoo as a preferred source to see more of our stories on Google. The U.S. Food and Drug Administration plans to change how COVID vaccines and other shots are approved and administered. The memo, ...
Public health, explained: Sign up to receive Healthbeat’s free national newsletter here. Six days after a senior Food and Drug Administration official sent a sweeping internal email claiming that ...
The Food and Drug Administration Wednesday abruptly and unexpectedly cancelled a planned March 13 vaccine advisory committee meeting that was to have chosen the flu strains in next year's U.S. flu ...
Greenwich's $3.81 million cash position covers less than two months of operations, making near-term financing highly likely ...
A senior Food and Drug Administration official on Friday said the agency will change its vaccine approval process, alleging that COVID-19 vaccination resulted in the deaths of 10 children.Video above: ...
Six days after a senior FDA official sent a sweeping internal email claiming that covid vaccines had caused the deaths of “at least 10 children,” 12 former FDA commissioners released an extraordinary ...
The elevation of longtime vaccine critics such as Malone and Levi to positions of influence in the ACIP is “unfortunate,” according to Robert Hopkins, M.D., an infectious disease physician and the ...
The US Food and Drug Administration has issued emergency use authorization (EUA) for the Covid-19 vaccine developed by Pfizer and BioNTech. After months of development, emergency use was authorized ...
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