Moderna files for emergency use authorization from the FDA to use its Covid-19 vaccine in adolescents ages 12 to 17. If cleared by the FDA, Moderna will become the 2nd vaccine available in the US for teens under 18.
Moderna has filed for FDA emergency use authorization of its Covid-19 vaccine for kids ages 12 to 17, which could expand the number of shots available to middle and high school students across the country. NBC News’ Dr. John Torres has the latest.
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Well this has been one way to reduce world wide population...The people that run the world and our lives have trying to figure put how to do it forever...They want young healthy workers for their country & do away with the sickly & poor. Without drawing attention to themselves A lot of pressure nice Is it an emergency for this age group range to be trying a vaccine that has no longitudinal study?
Moderna asks FDA to clear Covid vaccine for adolescents 12 to 17If approved, it would likely dramatically expand the number of Covid vaccine shots available to middle and high school students ahead of the next school year.
Moderna Asks FDA For Emergency Approval Of Its Covid-19 Vaccine In Teens Aged 12-17Moderna announced that it has filed a request with the FDA for Emergency Use Authorization of its Covid-19 vaccine in teens aged 12-17
Moderna seeks FDA authorization for Covid-19 vaccine for people ages 12 to 17Moderna has filed with the US Food and Drug Administration for emergency use authorization for its Covid-19 vaccine for people ages 12 to 17, according to a news release from the company.
Moderna’s Covid-19 Vaccine Seeks FDA Authorization for Use in AdolescentsModerna asked the FDA to authorize expanding the use of its Covid-19 vaccine to people as young as 12. The application means Moderna’s shot could be cleared for use in the older children this summer. 157,076,436 of 174,054,973 global covid-19 CASES recovered. Covid-19 CASES recover because they have natural efficacious immunoglobulin. So find out if you're immunoglobulin efficacy POSITIVE. Ask which (IET) covid-19 immunoglobulin efficacy test is right for you. There's a deafening silence around discussing natural immunoglobulin efficacy. Allopathic medical leaders recognised this efficacy in asymptomatic super spreaders. Why won't front line allopathic experts investigate how asymptomatics' efficacious immunoglobulin repels covid-19?
Two members of FDA panel resign in protest over Alzheimer's drug approvalThe 11-member committee voted nearly unanimously in November that Biogen's drug should not be approved, citing inconclusive evidence.
Johnson & Johnson says FDA has approved extended vaccine expiration dateJohnson & Johnson announced Thursday that the Food and Drug Administration (FDA) has authorized an extension of its COVID vaccine's shelf life from three months to 4.5 months.Why it matters: Amid a slowdown in vaccine uptake, a number of state health officials had been sounding the alarm that hundreds of thousands of single-shot J&J doses could expire this month.Get market news worthy of your time with Axios Markets. Subscribe for free.Prior to the FDA's extension, which the agency confirmed to