(HealthDay)—Pharmaceutical giant Merck & Co. said Friday that it will seek federal approval for emergency use of its new antiviral pill molnupiravir, after a clinical
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Emergency department visit rates because of an opioid overdose increased by 28.5% across the U.S. in 2020, compared to 2018 and 2019, recent Mayo Clinic
Read moreAt the beginning of prioritized health care personnel (HPC) immunization, there was a high rate of COVID-19 vaccine acceptance and receipt, with physicians and advance
Read moreThursday, December 10, 2020 FDA expected to make a decision on Emergency Use Authorization in the coming days Positive vote based on totality of scientific
Read moreWhat does emergency use of a COVID-19 vaccine mean? It’s when regulators allow shots to be given to certain people while studies of safety and
Read moreAmericans were on Friday facing a growing raft of coronavirus restrictions, even as pharma giant Pfizer and partner BioNTech prepared to file an emergency request
Read moreLockdowns may actually harm economy, health of country: Dr. Ramin Oskoui Foxhall Cardiology CEO Dr. Ramin Oskoui and oncologist Dr. William Grace discuss Biden coronavirus
Read moreIn a paper published Friday by the Journal of the American Medical Association, Virginia Commonwealth University researchers released data showing an alarming surge in opioid-related
Read morePeru on Friday extended its national emergency until September 30 and prolonged a lockdown in some of the areas worst affected by the coronavirus, the
Read moreThe U.S. Food and Drug Administration has authorized a new, rapid antigen test for COVID-19, which costs $5 and can diagnose an infection in 15
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