The AMA said it will research improved methods to prepare children for a tragic possibility without traumatizing them. The gun policy says schools should use “evidence-based and trauma-informed” approaches to train kids how to respond to active shooters in a way that minimizes unintended effects on mental health. | AP PhotoĭOCTORS’ GROUP TALKS GUNS, BURNOUT AND ABORTION - At its annual meeting this week, the American Medical Association adopted a new firearm violence policy focused on children’s mental health and gun safety, as well as physician burnout. The AMA is worried about practitioner burnout. children ages 5 to 11 were fully vaccinated, compared with nearly 56 percent of 12- to 15-year-olds and 67 percent of 16- and 17-year-olds, according to the CDC. But: It’s unclear whether any of it will do much to increase the number of American adolescents and kids who are vaccinated against Covid. Up next: Today, the committee will consider Moderna’s vaccine for children ages 6 months through 5 years, which would be a 25-microgram dose, alongside Pfizer-BioNTech’s bid to vaccinate kids under 5. The FDA said in a briefing document published last week that the shot was generally safe and effective in both groups. The group of independent advisers agreed that the benefit of increasing those options outweighed any risk the vaccine poses to children in the two age groups, 12- to 17-year-olds and 6- to 11-year-olds. The move brings American families one step closer to having more choices for vaccinating children. What’s next: Murray declined to lay out a specific timeline for next steps for the user fee package, saying she plans to work with Senate Majority Leader Chuck Schumer (D-N.Y.) on floor timing.įDA ADVISERS RECOMMEND MODERNA VACCINE - The Food and Drug Administration’s advisers voted unanimously on Tuesday to recommend authorizing Moderna’s Covid-19 vaccine for kids ages 6- to17 years, POLITICO’s Lauren Gardner reports. The current five-year FDA user fee agreement expires at the end of September. In exchange, the agency pledges to hire additional review staff and expeditiously review product applications. The package would enable the FDA to collect fees from manufacturers of brand drugs, generic drugs, biosimilars and medical devices for another five years. They aren’t present in the bill’s House version, which passed on the floor in a 392-28 suspension vote last week. Chair Patty Murray (D-Wash.) told POLITICO that the Senate intends to make sure the amendments make it into the final bill. The bill - considered to be must-pass legislation - was amended to include provisions aimed at preventing future baby formula shortages, among other issues. HELP COMMITTEE ADVANCES UFA- The Senate HELP Committee advanced its Food and Drug Administration user fee reauthorization package on Tuesday, POLITICO’s Katherine Ellen Foley and David Lim report. Patty Murray gives an opening statement during a Senate Appropriations Subcommittee hearing.
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