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FDA authorizes first COVID-19 pill treatment, Pfizer's Paxlovid - Vimarsana News

FDA authorizes first COVID-19 pill treatment, Pfizer's Paxlovid

The decision by the U.S. Food and Drug Administration comes as the omicron coronavirus variant has now officially reached each state in the union.

Source: wcvb.com
MSNBC Hallie Jackson Reports August 23, 2021 14:15:00 - Vimarsana News

MSNBC Hallie Jackson Reports August 23, 2021 14:15:00

Reporting on this. really appreciate it, a big day when it comes to the fda authorization for the pfizer vaccine. so with that, i want to bring in msnbc medical contributor dr. azar. that was a good conversation i had with kerry and with morgan and with cal, because it really kind of paints the picture of what we're dealing with across the country. there's some optimism as there should be with this fda authorization, but cal brings up a good point. there are some folks who say, i'm good, i'm healthy. i don't need this thing no matter what. how optimistic are you especially in your anecdotal re...

Houston Methodist Employees Sue To Stay Un-Vaxxed And Keep Their Jobs - Vimarsana News

Houston Methodist Employees Sue To Stay Un-Vaxxed And Keep Their Jobs

Houston Methodist Nurse Jennifer Bridges told the Houston Press in April she wasn’t willing to take a COVID-19 vaccine to keep her job. Now, Bridges and dozens of her coworkers are fighting back against the hospital chain’s vaccine requirement in court. On Friday, 117 Houston Methodist employees sued the hospital...

Johnson & Johnson vaccine: CDC advisory committee recommends shot for people 18 and older - Vimarsana News

Johnson & Johnson vaccine: CDC advisory committee recommends shot for people 18 and older

A U.S. advisory panel has endorsed the new one-dose COVID-19 vaccine from Johnson & Johnson as a third option to bolster the national effort against the coronavirus pandemic.

Source: abc7ny.com
First direct-to-consumer coronavirus test gets FDA authorization - Vimarsana News

First direct-to-consumer coronavirus test gets FDA authorization

First direct-to-consumer coronavirus test gets FDA authorization and last updated 2020-12-09 23:20:03-05 For the first time, the FDA has authorized coronavirus tests that can be sold directly to Americans who do not have to go through a health care provider. An emergency use authorization is not a full approval from the FDA, but allows the tests to be used in a non-clinical or non-hospital setting. The LabCorp’s Pixel COVID-19 Test Home Collection Kit can be used by any adult age 18 or over. The test kit allows individuals to take a nasal swab at home and send the sample to LabCorp for t...

Source: 10news.com