As the country fights a wave of new infections, the Food and Drug
Administration authorized two medications this week that could ward off the
virus' worst effects.
Pfizer's
Paxlovid pill reduces the chance of hospitalization and
death by 90 percent in high-risk patients. Supplies are limited, but the
medication is now approved for adults and children ages 12 and older with a
positive COVID-19 test and early symptoms.
“The efficacy is high, the side effects are low and it’s oral. It checks all
the boxes,” said Dr. Gregory Poland of the Mayo Clinic to the Associated Press.
And Merck's pill,
likely to become the second-choice treatment, is less effective at combating
severe illness. Its drug label will also warn of serious safety issues,
including potential birth defects.
The approval comes just in time. Researchers have found that two of the three
monoclonal antibody treatments doctors depend on to treat COVID patients are ineffective against
Omicron.
To be a Medicare Agent's source of information on topics affecting the agent and their business, and most importantly, their clientele, is the intention of this site. Sourced from various means rooted in the health insurance industry - insurance carriers, governmental agencies, and industry news agencies, this is aimed as a resource of varying viewpoints to spark critical thought and discussion. We welcome your contributions.
Saturday, February 26, 2022
FDA authorizes two pills to fight COVID-19
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment