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FDA Advisory Panel Says Yes to Pfizer’s COVID Vaccine

The Pharma Data

Centers for Disease Control and Prevention will also vote on whether to recommend the vaccine and for whom, the Post reported. First in line are health care personnel and residents and staff of long-term care facilities, according to earlier recommendations released by the CDC panel.

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Biden Will Ask Americans to Wear Masks for 100 Days

The Pharma Data

As for Fauci, Biden made it clear that the nation’s top infectious diseases expert would be a central player in the U.S. Doctors say this reflects India’s younger and leaner population. Just 100 days to mask — not forever, just 100 days. coronavirus response, The New York Times reported.

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CDC Director Warns of Dire Winter Ahead for COVID Hospitalizations, Deaths

The Pharma Data

Centers for Disease Control and Prevention warned Wednesday that the coming winter months might be the darkest period yet in the coronavirus pandemic. Doctors say this reflects India’s younger and leaner population. THURSDAY, Dec. 3, 2020 – The head of the U.S. An FDA advisory panel is set to meet on Dec.

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Britain Approves Emergency Use of Pfizer’s COVID Vaccine

The Pharma Data

The recommendation from the Advisory Committee on Immunization Practice (ACIP), if heeded, will steer the initial short supply of vaccines to about 21 million health care personnel and 3 million Americans working or living in long-term care facilities.

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Lilly’s Neutralizing Antibody Bamlanivimab (LY-CoV555) Receives FDA Emergency Use Authorization for the Treatment of Recently Diagnosed COVID-19

The Pharma Data

“This emergency authorization allows us to make bamlanivimab available as a COVID-19 treatment for recently diagnosed, high-risk patients – adding a valuable tool for doctors fighting the now-increasing burden of this global pandemic,” said David A. Ricks, Lilly’s chairman and CEO. patients who recovered from COVID-19. .

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New Data Show Treatment with Lilly’s Neutralizing Antibodies Bamlanivimab (LY-CoV555) and Etesevimab (LY-CoV016) Together Reduced Risk of COVID-19 Hospitalizations and Death by 70 Percent

The Pharma Data

Lilly has received feedback from front-line nurses and doctors administering these infusions regarding the complexity and time requirements for preparation and administration. It remains under review by the FDA. It was identified from a blood sample taken from one of the first U.S. patients who recovered from COVID-19. . www.lilly.com?and?www.lilly.com/news.?P-LLY.

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COVID-19 Vaccine Developers Adjust Phase 3 Trial Protocols to Allow Authorized Vaccines | 2020-12-17

The Pharma Data

It’s going to change everyone’s behavior otherwise,” suggested Hayley Gans, a pediatrics and infectious diseases expert at Stanford University Medical Center. This would mean volunteers who already received a vaccine would be given a placebo and vice versa, allowing companies to evaluate their product’s safety and long-term efficacy.

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