"That baseline of protection should be enough, the agency says, to move to an annual booster against the latest strains in circulation and make COVID-19 vaccinations more like the yearly flu shot."

>F.D.A. AUTHORIZES REFORMULATED COVID-19 BOOSTER Shots, TARGETING OMICORN SUBVARIANTS.

The New York Times: Biden Administration Plans for Booster Shot Campaign in September. >"A top F.D.A. regulator cited compelling data for redesigned _...Read More_

"A new medication called Auvelity was just FDA-approved to treat major depressive disorder (MDD), also known as clinical depression, in as little as one week. The new “fast-acting” oral drug for clinical depression, from Axsome _...Read More_

"The Food and Drug Administration plans to authorize updated versions of Pfizer-BioNTech’s and Moderna’s Covid boosters around Labor Day, said two people familiar with the discussions."

"Moderna submitted its application to the US Food and Drug Administration for emergency use authorization of its updated Covid-19 vaccine booster for use in people age 18 and older the company said in a news release on Tuesday."

"The US Food and Drug Administration authorized Novavax's Covid-19 vaccine on Friday for emergency use in adolescents. It is the fourth coronavirus vaccine available in the United States and, unlike the others, is uses a protein-based _...Read More_

>"The agency’s action opens the door to cheaper, more accessible devices without a prescription or medical exam."

CNBC: FDA expands monkeypox vaccine authorization to increase dose supply, allows shots for children. >"The FDA will allow _...Read More_

Is it all about more and more doses? Are these vaccines having actual effects and achieving the expected results (even to an extent)? If the variant attack on the population remains high even with every updated booster shots, people are _...Read More_

Why not received reward?

The New York Times: Biden Administration May Offer Second Coronavirus Boosters to All Adults. >"The latest, highly contagious variant has driven up hospitalization _...Read More_

“This is good news,” Susan F. Wood, a former assistant commissioner for women’s health at the FDA and now director of George Washington University’s Jacobs Institute of Women’s Health Services, said in an email. She said she hoped the FDA _...Read More_

CNN: FDA setting up process to allow foreign formula manufacturers to permanently sell products in US. >"The US Food and Drug Administration announced plans _...Read More_

Making the access road to Paxlovid easier through licensed pharmacists for patients that need it is a move in the right direction. Because a drug you need to take that fast (within 5 days of symptoms) should also be easily accessible _...Read More_