The New York Times, December 15, 2020 (with Noah Weiland and Denise Grady)

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WASHINGTON — The coronavirus vaccine made by Moderna is highly protective, according to new data released on Tuesday, setting the stage for its emergency authorization this week by federal regulators and the start of its distribution across the country.

The Food and Drug Administration intends to authorize emergency use of the vaccine on Friday, people familiar with the agency’s plans said. The decision would give millions of Americans access to a second coronavirus vaccine beginning as early as Monday. The Pfizer-BioNTech vaccine, cleared last week, was the first to be authorized.

Continue reading “Moderna Vaccine Is Highly Protective Against Covid-19, the F.D.A. Finds”

The New York Times, December 8, 2020 (with Noah Weiland)

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WASHINGTON — The coronavirus vaccine made by Pfizer and BioNTech provides strong protection against Covid-19 within about 10 days of the first dose, according to documents published on Tuesday by the Food and Drug Administration before a meeting of its vaccine advisory group.

The finding is one of several significant new results featured in the briefing materials, which include more than 100 pages of data analyses from the agency and from Pfizer. Last month, Pfizer and BioNTech announced that their two-dose vaccine had an efficacy rate of 95 percent after two doses administered three weeks apart. The new analyses show that the protection starts kicking in far earlier.

Continue reading “Pfizer’s Vaccine Offers Strong Protection After First Dose”

The New York Times, December 8, 2020 (with Benjamin Mueller)

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Britain’s National Health Service began delivering shots of the Pfizer-BioNTech vaccine on Tuesday, opening a public health campaign with little precedent in modern medicine and making Britons the first people in the world to receive an authorized, fully tested vaccine.

Here’s a guide to some of the basics.

Continue reading “U.K. Coronavirus Vaccine: Side Effects, Safety, and Who Gets It First”

It’s just a few weeks since I sat down to write my last newsletter, and yet it feels like another century of history has elapsed. The United States is skyrocketing back to the worst rates of hospitalizations and deaths of the spring. On December 3 alone, 2,857 Americans died. That’s just shy of the total number of people who died on 9/11–a disaster that still scars us 19 years later. As winter sets in and people stay inside more, things are only going to get worse. I have no idea how deep the scars from this pandemic will run.

It is deeply disorienting to spend this terrible time reporting indisputably good news. When I sent out November’s newsletter, Pfizer had just announced that the efficacy of its vaccine was over 90 percent, which was pretty staggering. Since then, a subsequent analysis of more cases of Covid-19 in their trial zeroed in on a figure of 95 percent. Moderna’s vaccine turned out to have an efficacy rate at 94.5 percent. The newest look at the trial for Sputnik V from Russia puts theirs at 91 percent. AstraZeneca, at least in one version of its dosing, is 90 percent. Continue reading “Friday’s Elk, December 5, 2020”

The New York Times, December 5, 2020

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Across the world, mass vaccination campaigns are beginning, or just about to.

Russia began its campaign on Saturday. Britain will start its campaign on Tuesday. The United States hopes to start large-scale vaccinations this month, as does Turkey. Hundreds of thousands of people have already been vaccinated in China, and thousands in the United Arab Emirates and elsewhere.

But the mass vaccination efforts differ in one profound way: Some rely on a vaccine that has completed human trials — and some do not.

Continue reading “Mass vaccinations are beginning. They’re not all the same.”