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Saturday, November 21, 2020 at 09:44 PM
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The U.S Food and Drug Administration is authorizing Regeneron's antibody cocktail for some patients who test positive for COVID-19. [Read More]
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The U.S Food and Drug Administration is authorizing Regeneron's antibody cocktail for some patients who test positive for COVID-19. [Read More]
The U.S Food and Drug Administration is authorizing Regeneron's antibody cocktail for some patients who test positive for COVID-19. [Read More]
The Food and Drug Administration has granted emergency authorization for the experimental antibody treatment given to President Donald Trump shortly after he was diagnosed with... [Read More]
The U.S. Food and Drug Administration (FDA) on Saturday granted emergency authorization for the antibody treatment administered to and later praised by President Trump for his past... [Read More]
The U.S. Food and Drug Administration is authorizing Regeneron's antibody cocktail for some patients who test positive for COVID-19. [Read More]
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The U.S. Food and Drug Administration has given the green light for emergency use of Regeneron's COVID-19 antibody drug — the same treatment given to... [Read More]
SILVER SPRING, Md., Nov. 21, 2020 /PRNewswire/ -- Today, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for casirivimab and imdevimab... [Read More]
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The U.S. Food and Drug Administration on Saturday said it will allow for the emergency use of Regeneron's Covid-19 antibody treatment, the New York Times... [Read More]
The Food and Drug Administration has granted emergency authorization for the experimental antibody treatment given to President Donald Trump shortly after he was diagnosed with... [Read More]
The U.S. Food and Drug Administration on Saturday granted emergency authorization to the experimental antibody treatment given to President Donald Trump last month when he... [Read More]
The Food and Drug Administration has granted emergency authorization for the experimental antibody treatment given to President Donald Trump shortly after he was diagnosed with... [Read More]
Today, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for casirivimab and imdevimab to be administered... [Read More]
The Food and Drug Administration (FDA) has granted an emergency use authorization for a promising new drug cocktail for hospitalized CCP virus patients. [Read More]
By The Associated Press It's when regulators allow shots to be given to certain people while studies of safety and effectiveness are ongoing. ... [Read More]
Pfizer asked the Food and Drug Administration for emergency use authorization for its COVID-19 vaccine on Friday. The vaccine could be available in December, but... [Read More]
Savannah's Dr. Paul Bradley, who in July dosed the first patient in biotechnology company Moderna's U.S. phase 3 COVID-19 vaccine trial, on Monday celebrated the... [Read More]
The U.S. Food and Drug Administration has now authorized emergency use of an antibody cocktail treatment produced by Regeneron to help the immune system fight... [Read More]
Eli Lilly and Company announced the U.S. Food and Drug Administration (FDA) issued an Emergency Use Authorization (EUA) for the distribution of baricitinib. The authorization... [Read More]
Eli Lilly and Company announced the U.S. Food and Drug Administration (FDA) issued an Emergency Use Authorization (EUA) for the distribution of baricitinib. The authorization... [Read More]
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