• Mashup Score: 2

    The FDA has for the first time approved an emergency use authorization for a long-acting monoclonal antibody cocktail designed to prevent symptomatic COVID-19 among adults and children aged 12 years and older. According to data submitted to the FDA, AstraZeneca’s Evusheld (tixagevimab plus cilgavimab), also known as AZD7442, when sued The pre-exposure prophylaxis, can reduce the risk for

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    • The #FDA has approved an emergency use authorization for #AstraZeneca's long-acting monoclonal antibody cocktail designed to prevent symptomatic #COVID19 in adults and children aged 12 years and older. Comments from @alhkim, perspective from @LCalabreseDO https://t.co/lJP8dYaOGb

  • Mashup Score: 21

    Fears of adverse effects of COVID-19 vaccination on fertility have affected vaccine uptake in some communities. Despite the absence of supporting evidence for such a risk, low biological plausibility, and preliminary data supporting the safety of mRNA vaccines in pregnancy,1–3 this claim has become widespread, and it has been challenged by WHO.4 Vaccine hesitancy during pregnancy, or among women…

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    • New research letter: Fertility rates and birth outcomes after ChAdOx1 nCoV-19 (AZD1222) vaccination. Authors analysed pregnancies occurring in four ongoing clinical trials in the UK, Brazil, and South Africa. https://t.co/hDM1olKts9 @OxfordVacGroup | #COVID19 #AstraZeneca https://t.co/m5qvWhPcph

  • Mashup Score: 1

    The drug reduced the risk of severe COVID-19 or death by 50% in non-hospitalized patients who have had symptoms for seven days or less.

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    • #AstraZeneca’s new drug, a combination of 2 #antibodies called AZD7442, reduced the risk of severe COVID-19 or death by 50% in non-hospitalized patients who have had symptoms for 7 days or less, according to a company statement. https://t.co/sVFf8d3njg https://t.co/QinHURaxQn