The move gives doctors and high-risk patients an additional option for treating mild-to-moderate illness caused by the coronavirus.

BING NEWS:
  • In a first, FDA authorizes AI-driven test to predict sepsis in hospitals
    Now, the Food and Drug Administration has greenlighted such ... that opened his eyes to how many people die of it. “This is going to be what we do,” he said. At least 1.7 million adults ...
    04/3/2024 - 10:31 am | View Link
  • U.S. FDA approves Akebia's anemia drug
    opens new tab drug, vadadustat, to treat anemia caused by chronic kidney disease (CKD) in dialysis patients, the drugmaker said on Wednesday. The drug will be available under the brand name Vafseo ...
    03/28/2024 - 3:17 am | View Link
  • FDA approves Merck & Co’s pulmonary arterial hypertension drug sotatercept
    In this trial, all patients were on stable background therapy, and over half of the participants ... That’s very exciting,” says Hassoun. The drug also hit eight out of nine secondary end ...
    03/26/2024 - 1:00 pm | View Link
  • FDA approves new drug that may help stop a rare, fatal condition that doctors call a ‘ticking time bomb’
    Then her medical team offered her a potential lifeline: a first-of-its-kind experimental drug called sotatercept that corrals a growth factor that is overproduced by people with PAH, potentially ...
    03/25/2024 - 1:00 pm | View Link
  • FDA Approves Merck’s New Drug For A Rare Lung Disease
    The vast majority of people with this disease are women, and they are disproportionately Black or Hispanic. On Tuesday, the Food and Drug Administration approved a new drug to treat this disease ...
    03/25/2024 - 1:00 pm | View Link
  • More

 

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