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U.S. FDA authorizes sale of first home COVID/flu combo test outside of emergency use

As the country heads into the respiratory illness season, the US Food and Drug Administration (FDA) announced yesterday its marketing authorization of the first over-the-counter (OTC) rapid-antigen COVID-19/flu combination test outside of emergency use authorization.

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Efforts to reduce barriars to RSV shots now that CDC has recomended vacinations

When the Food and Drug Administration approved several new vaccines against respiratory syncytial virus last year, the shots were celebrated as a “powerful new tool” to protect infants and older people. Pharmaceutical giants projected billions of dollars in sales, assuming a large swath of the eligible population would roll up their sleeves.

But for all the anticipation, relatively few people sought the vaccines out: Only about 24 percent of eligible older adults received it last season. It was a disappointing response, one experts blamed largely on vaccine fatigue, the cost of the shots and confusion over who should get them.

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