Editor’s note: Find the latest COVID-19 news and guidance in Medscape’s Coronavirus Resource Center. The US Food and Drug Administration (FDA) has granted Eli Lilly’s request to revoke emergency use authorization for the COVID-19 monoclonal antibody therapy bamlanivimab when used as a monotherapy, saying the evidence indicates that it is likely not effective against currently circulating
A company-initiated recall of two models of EMBLEM S-ICD (Boston Scientific) subcutaneous implantable cardioverter defibrillator pulse generators has been categorized as Class I by the US Food and Drug Administration (FDA), the agency announced today. The FDA notes that the advisory, which was communicated to patients and doctors in December, applies to 2825 of the
Editor’s note: Find the latest COVID-19 news and guidance in Medscape’s Coronavirus Resource Center. Last week, Anthony Fauci, MD, said that “virtually everybody and anybody in any category could start to get vaccinated” in April. But on Tuesday, the Biden administration changed the timeline for mass vaccinations to May, June, or July. At a CNN
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