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The long view on COVID-19 vaccine safety and efficacy

Penn researchers weigh in on the regulatory and scientific efforts to track COVID-19 vaccines. Between December 2020 and February 2021, three drugmakers received Emergency Use Authorizations to distribute COVID-19 vaccines. The next step is a biologics license application the technical name for full approval a process Pfizer and Moderna have already begun. Experts from Penn are keeping a close eye on these regulatory steps, as well as the reporting mechanisms involved in assessing vaccine safety. The outlook thus far seems promising. (Image: Daniel Schlud) The mRNA vaccines for COVID-19, made by Pfizer/BioNTech and Moderna, are among the most powerful vaccines the world has ever seen. According to clinical trial data, they are more than 94% effective at preventing symptomatic disease, with real-world data bearing out that success. The other vaccine currently available in the U.S., produced by Janssen, uses a viral

Sarasota schools to be mask-optional in fall, if board approves rule

School board member Tom Edwards said he is comfortable with making masks optional. The new policy applies to anyone on school grounds, regardless of vaccination status.  “If you’re an adult or a child that’s old enough to be vaccinated and you choose not to be vaccinated, and you choose not to wear a mask and you get sick, that seems to be more your responsibility than someone else’s,” Edwards said. “If it looks to become a problem, you can have an emergency mask policy if you needed it.” The Centers for Disease Control updated its guidance for schools on July 9, recommending that unvaccinated people should continue to wear masks indoors. That would include all children under the age of 12 since none of the current vaccines are approved for them yet. 

Point & counterpoint | Mandating vaccine: Chris Talgo - Children shouldn t be a testing ground

Point & counterpoint | Mandating vaccine: Chris Talgo - Children shouldn t be a testing ground
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