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Trump on FDA Authorizing COVID-19 Vaccine: ‘A Medical Miracle’

Trump on FDA Authorizing COVID-19 Vaccine: ‘A Medical Miracle’

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Trump on FDA Authorizing COVID-19 Vaccine: ‘A Medical Miracle’

by Madison Summers
December 12, 2020 at 7:50 am
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President Donald Trump is offering praise after the U.S. Food and Drug Administration (FDA) issued emergency use authorization for Pfizer/BioNTech’s COVID-19 vaccine.

In a video posted to Twitter on Friday, Trump said, “Today our nation has achieved a medical miracle.”

He continued, “We have delivered a safe and effective vaccine in just nine months. This is one of the greatest scientific accomplishments in history. It will save millions of lives and soon end the pandemic once and for all.”

The president also applauded those who worked to make “this all possible.”

“On behalf of the American people, I’d like to thank all of the brilliant scientists, technicians, doctors and workers who made this all possible.”

In the press release announcing the emergency use authorization of the first coronavirus vaccine, FDA Commissioner Stephen M. Hahn called it “a significant milestone in battling this devastating pandemic that has affected so many families in the United States and around the world.”

Watch the video below:

pic.twitter.com/ofLq3OMicv

— Donald J. Trump (@realDonaldTrump) December 12, 2020

Today, FDA issued the first emergency use authorization (EUA) for a vaccine for the prevention of #COVID19 caused by SARS-CoV-2 in individuals 16 years of age and older. The emergency use authorization allows the vaccine to be distributed in the U.S. https://t.co/1Vu0xQqmCB pic.twitter.com/c8maeePP9O

— U.S. FDA (@US_FDA) December 12, 2020

The FDA has determined that the #COVID19 vaccine has met the statutory criteria for issuance of an EUA. The totality of the available data provides clear evidence it may be effective in preventing COVID-19.

— U.S. FDA (@US_FDA) December 12, 2020

In making this determination, the FDA can assure the public and medical community that it has conducted a thorough evaluation of the available safety, effectiveness and manufacturing quality information.

— U.S. FDA (@US_FDA) December 12, 2020

Additionally, FDA’s Center for Biologics Evaluation and Research Peter Marks said in a statement, “While not an FDA approval, today’s emergency use authorization of the Pfizer-BioNTech COVID-19 Vaccine holds the promise to alter the course of this pandemic in the United States.”

House Speaker Nancy Pelosi (D-Calif.) also applauded scientists and doctors following the news of the FDA’s authorization.

She wrote in a statement late Friday, “Today’s Emergency Use Authorization of the Pfizer vaccine is a tribute to the tireless efforts of scientists and doctors who have worked around the clock to ensure that we have a vaccine that is effective and safe.”

The House speaker also encouraged Americans to have “full confidence in this vaccine.”

She added, “Now, with tonight’s FDA authorization, we must ensure that the vaccine will be free and distributed in a fair and equitable manner to as many Americans as possible as soon as possible.” Pelosi also called for the Defense Production Act to be invoked.

“Until the vaccine is widely available, it is essential that we continue to embrace the testing, tracing, treatment, mask wearing and social distancing that are essential to preventing thousands of Americans from dying every day from the pandemic,” Pelosi wrote.

According to a Reuters/Ipsos poll, conducted Dec. 2-8, it found that women in the U.S. are more hesitant to get the coronavirus vaccine than men. While roughly 55% of women surveyed said they would be “very” or “somewhat” interested in getting the vaccine, 68% of men said they would.

This comes as the U.S. continues to combat the coronavirus pandemic. There have been 207,816 COVID-19 cases on average reported per day over the past week. This is a 25% increase from the two weeks prior, according to The New York Times.

Tags: Coronavirus OutbreakDonald TrumpFood and Drug AdministrationNancy Pelosi
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Madison Summers

Madison Summers

IJR, Managing Editor

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