FDA

The Food and Drug Administration on Friday issued an emergency use authorization for Moderna’s Covid-19 vaccine, clearing the way for it to be the second vaccine distributed in the United…

The Food and Drug Administration moved Friday to grant an emergency use authorization to drugmaker Moderna’s coronavirus vaccine, the second one approved for use in the U.S. The agency’s decision…

The Food and Drug Administration has approved Moderna’s coronavirus vaccine for emergency use. The vaccine — the second approved for use in the U.S. behind Pfizer and BioNTech’s — bolsters…

An advisory committee to the Food and Drug Administration voted on Thursday 20-to-0, with one abstention, to recommend the Moderna Covid-19 vaccine for an emergency use authorization for people ages…

By: New York Times | Updated: December 18, 2020 10:26:27 am The headquarters of the pharmaceutical firm Moderna in Cambridge, Mass., on Nov. 19, 2020. Moderna’s coronavirus vaccine has the…

Moderna is developing eight other vaccines that use mRNA. The company has tested them in animals and in 1,700 people, and has not had cases of anaphylaxis or other severe…

Here’s what’s happening Thursday with the coronavirus pandemic in the U.S.: THREE THINGS TO KNOW TODAY A second COVID-19 vaccine moved closer to joining the U.S. fight against the pandemic…

An influential Food and Drug Administration advisory panel on Thursday overwhelmingly backed Moderna’s coronavirus vaccine, a key step paving the way to distribute the second Covid-19 vaccine in the United…

This is the same committee of expert advisers that last week backed the COVID-19 vaccine from Pfizer Inc. and German partner BioNTech SE. A panel of outside advisers to the…

On Sunday, the first batches of the Pfizer-BioNTech Covid-19 vaccine were loaded onto trucks and cargo planes to be distributed around the United States. Doses of the vaccine, which received…

The Food and Drug Administration authorized Pfizer’s Covid-19 vaccine for emergency use on Friday, clearing the way for millions of highly vulnerable people to begin receiving the vaccine within days.…

In a video statement released on , Trump also said that the vaccine would be free for all Americans File photo of Donald Trump. AP Washington: President Donald Trump said…

The Food and Drug Administration on Friday evening granted an emergency use authorization (EUA) to the Covid-19 vaccine developed by Pfizer and BioNTech, making it the first Covid-19 vaccine in…

The Food and Drug Administration has approved Pfizer and BioNTech’s coronavirus vaccine for emergency use, a monumental turning point in the once-in-a-century pandemic that has taken nearly 300,000 American lives…

U.S. President Donald Trump and Stephen Hahn, Director of the Food and Drug Administration participate in the daily coronavirus task force briefing at the White House on April 24, 2020…

White House chief of staff Mark Meadows told Stephen Hahn his job was in jeopardy if the emergency use authorization was not issued before Saturday White House chief of staff…

A vial of the Pfizer/BioNTech COVID-19 vaccine is seen ahead of being administered at the Royal Victoria Hospital in Belfast, Northern Ireland December 8, 2020. Liam McBurney | Pool |…

An advisory committee to the Food and Drug Administration has voted 17 to 4, with 1 abstention, to recommend emergency use authorization to the first vaccine for Covid-19 in the…

A panel of outside advisers to the U.S. Food and Drug Administration on Thursday voted overwhelmingly to endorse emergency use of Pfizer Inc’s coronavirus vaccine, paving the way for the…

Pfizer’s Covid-19 vaccine passed a critical milestone on Thursday when a panel of experts formally recommended that the Food and Drug Administration authorize the vaccine. The agency is likely to…

Pfizer Inc said on Thursday it planned to file for full U.S. approval of its experimental coronavirus vaccine by April next year, even as the vaccine awaits emergency use authorization…

As per a senior administration official, the order would restrict the federal government from ivering doses to other nations until there supply outstrips domestic demand Washington: President Donald Trump celebrated…

Raising hope of granting emergency use authorisation to drugmakers Pfizer and BioNTech’s experimental Covid-19 vaccine, the US Food and Drug Administration (FDA) said on Tuesday that data from 38,000 trial…

Healthcare workers and others recommended for the first COVID-19 inoculations could start getting shots within 24 hours after the vaccine receives regulatory authorization, the chief adviser for the U.S. government’s…

Moderna said Monday it will request emergency clearance from the Food and Drug Administration for its coronavirus vaccine after new data confirms the vaccine is than 94% effective in…

Amid record levels of new Covid-19 infections and hospitalizations, the Food and Drug Administration announced Saturday that it would allow emergency use of an antibody drug treatment known as REGN-COV2…