Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.
Sponsored by
You're Probably Using the Wrong Credit Card…
With the right credit card, you could be earning hundreds - even thousands - of dollars in rewards every year. GigaPoints uses data, not guesses, to match you with the credit cards that will earn you the most points, based on the way you actually spend, so you can score cash back, free travel, and more. Best of all, it's fast, easy and free. Learn More.
“Britain approved Pfizer Inc’s COVID-19 vaccine on Wednesday, jumping ahead of the rest of the world in the race to begin the most crucial mass inoculation programme in history.” Reuters
Both sides celebrate the development of the vaccines, stress their safety, and call for politicians and celebrities to urge the public to take them:
“The story of how these new vaccines came to us so fast would make a thrilling documentary. The accomplishments of these private-sector teams of scientists is a culmination of progress across decades, not least the identification of messenger RNA 60 years ago. Today, biological science has so many moving parts that it takes multidisciplinary teams to produce products like the vaccines heading this month to the Food and Drug Administration for emergency approval…
“The intellectual, technical and organizational firepower of thousands of men and women employed by pharma is what made these savior vaccines happen in 10 months rather than years. They won’t ask for anyone’s gratitude, but they deserve it… This is the moment to put into nomination the obvious recipient for 2021’s Nobel Peace Prize: the scientists at the pharmaceutical companies whose vaccines are about to rescue the world from the catastrophe of SARS-CoV-2.”
Daniel Henninger, Wall Street Journal
“It’s true that the COVID-19 vaccines have been developed quickly, in particular when — as is sometimes claimed — vaccine development can take anything from seven to 10 years. But this doesn’t mean the vaccine is rushed or unsafe… Vaccine development involves a hard scramble for funding, dominated by commercial decisions, full of red tape and stupid delays like contract negotiations that drag on for years…
“For most of the 10 years it can take to develop a vaccine, you are not running a trial. You are not getting safety data. In fact, you would normally end up with a smaller safety dataset than we have in the pandemic because the trials this time around are so blockbuster big. We now know running these trials quickly was ‘easy’: you just needed unlimited money, all the world’s formidable trial infrastructure pointed at one question, a huge pool of altruistic volunteers and some focused regulators.”
Dr. Mark Toshner, Spectator USA
Regarding public skepticism, “The anti-vaccination movement learned its way around the Web long before covid-19 struck, and the disinformation war it has started even before these lifesaving medicines are widely available must be countered with a preemptive defense…
“Researchers have identified the importance of filling ‘data deficits’ to give people the right answers before opportunists can give them the wrong ones. This must occur in a manner that explains without overwhelming, as complexity can push people toward the comfort of simple answers no matter their veracity. The government needs to figure out how to communicate with the country’s citizens about vaccines frequently, specifically and sensitively, tailoring its messages to existing misconceptions as well as to different types of audiences.”
Editorial Board, Washington Post
“On October 28, 1956, a young Elvis Presley went on ‘The Ed Sullivan Show.’… The crowd screamed so loud you could barely hear him sing. But what really makes that night so memorable is that before his performance, viewers watched Presley get his polio vaccine on television. It made headlines and, critically, also helped convince teens and young adults -- people who thought they weren't at risk -- that they needed a vaccine too in order to help defeat the deadly disease… Celebrity leadership and activism can be overrated, but there are moments in which famous and trusted people can sway mass opinion in ways vital to the public good…
“Former presidents Obama, Bush and Clinton have all said they will take the vaccine publicly, which is great, but we're going to need to do a lot more than that… governors should all reach out to the stars of country music and pop, basketball and NASCAR, and get them on board. Beyonce and Jay-Z, Taylor Swift, the boys from BTS, LeBron James, Tom Brady, whomever we can. We're no longer in the concentrated media environment of the 1950s Sullivan show where a single star on a single station can shape the news of the nation, but the diversity of platforms and audiences can be a strength if everyone finds a known and trusted face within their media niche taking the vaccine.”
David M. Perry, CNN
Regarding vaccine distribution, Nirav Shah, Director of the Maine Center for Disease Control and Prevention, explains that “We began planning for COVID-19 vaccine distribution—in theory and in concept—back in mid-April… The first thing we did was we ordered freezers. We spent about $12,500 ordering two massive freezers for our central warehouse. The second thing is, back in September we did a needs assessment and needs inventory, so we already knew where in the health care system there were existing ultra-cold freezers… [In addition we found that] there are communities that don’t have hospitals in them, but for whatever reason they’ve got a community college that has an ultra-cold freezer…
“As to dry ice, one of the principal uses for dry ice in the United States is the packaging of seafood. The lobster industry is a large consumer of dry ice for their shipping and packaging. So dry ice is big in Maine, and we do not anticipate challenges with dry ice. We have mapped out everything, and now we’re focused on what is literally the last mile… If I showed up with a box of vaccines, I want to know how many vials you can accommodate in your ultra-cold storage freezer and still maintain -80°C. Another thing we’re working on is what we need for the first wave of vaccinators within health care systems: How many gloves are we going to need for them to handle the dry ice?… It’s all the things that you just never think about.”
Nirav Shah, Slate
Other opinions below.
“The United States had the private-sector capacity ready to go for this modern Manhattan Project for the same reason it was able to turn the Ford, General Motors, and Chrysler assembly lines to tank production in 1942: our dynamic free-market capitalist economy and, yes, its tolerance for massive for-profit pharmaceutical businesses. Pfizer financed the bulk of the estimated $2 billion research-and-development cost of its partnership with BioNTech out of its own prodigious balance sheet, which brings in $52 billion in revenue a year…
“We are endlessly told that America should be more like the rest of the world in the health-care sector, and that we could cut drug costs in particular by cracking down on Big Pharma’s profits. But now, once again, the rest of the world is getting a free ride on the dynamism of America’s health-care sector, which even for all of its government red tape is still one of the freest in the world. American free-market capitalism will save lives, as it has done so many times before, when nobody else could.”
Dan McLaughlin, National Review
“Unless someone can point to a deficiency in British scientific review, one does have to wonder why we have to wait eight more days for an FDA meeting to act on an emergency-use application. Did the FDA get the data from Pfizer eight days later? That seems unlikely, given how much incentive Pfizer had to get ahead of Moderna in its own race to produce the first approved vaccine…
“Critics have long complained about the FDA’s inefficiency and clumsy processes, and it looks like those might have cost us a couple of weeks of vaccinations, right as community spread is filling hospitals to the breaking point. This is more than an emergency — it’s a global disaster. Did the FDA respond to it properly, or did it stumble over its own bureaucracy in the home stretch?”
Ed Morrissey, Hot Air
“The FDA has long been cautious when approving new medicines, which has resulted in delayed treatments for life-threatening diseases like cancer. But its self-protective instinct and desire to compensate for reckless politicians endanger public health…
“[The FDA’s current] regulatory rigmarole is essentially a placebo to reassure the public it will be safe to get inoculated. There’s no evidence that a three-week review is needed. The U.K.’s Medicines and Healthcare products Regulatory Agency with 1,320 employees scrutinized Pfizer’s data on a rolling basis, and the FDA with 17,000 staff could do the same… Delaying vaccine approval even a couple of weeks could lead to thousands, if not tens of thousands, of more deaths.”
Editorial Board, Wall Street Journal
“Progress on vaccines means people can now plausibly talk about what they will do when the pandemic is over. But with new infections topping 212,000 Thursday — another daily record, topping one set Wednesday — it won’t be over in a snap…
“Officials in some states, including ones slammed badly by the virus, continue to resist issuing mask mandates or other restrictions, such as limiting indoor dining. But the CDC says these measures produce results. That’s been seen in North Dakota, where Gov. Doug Burgum (R) three weeks ago announced limits on indoor dining and a public mask mandate. Since then, the state’s average number of new cases has dropped from 1,400 per day to about 700 per day, according to data tracked by The Washington Post…
“It will take time to change the trajectory of the epidemic… It is impossible to know when life will get back to normal, or something that feels close to it. The vaccine rollout will take many months under even the most optimistic scenarios… The message from infectious disease experts and a growing number of governors and mayors is that everyone needs to mask up, stay at home as much as possible, and hang on.”
Joel Achenbach and Jose A. Del Real, Washington Post
“The White House, ever mindful of Trump's ‘America First’ mantra, is demanding the FDA move more quickly to authorize emergency use of the first two vaccine candidates from Pfizer and Moderna. (The United Kingdom granted emergency-use authorization for the Pfizer vaccine Wednesday.)…
“But it's counterproductive to rush the science and risk undermining public confidence in a vaccine when a Gallup poll shows that 42% of people are unwilling to be inoculated. FDA Commissioner Stephen Hahn wisely placed management of the process with seasoned career federal scientists to build public trust. The review process should be allowed to play itself out and do so transparently…
“It would [also] be unconscionable at this crucial juncture to give fiscally strapped states responsibility for financing the additional infrastructure, communication, outreach and hiring necessary to organize dissemination of the vaccines and persuade people to accept them. With hospitals buckling under the strain and daily COVID-19 deaths at 9/11 levels, Congress needs to set aside partisan differences in this emergency and immediately enact stimulus funding… America's leaders have one shot to deliver the country from this nightmare with a thorough and robust vaccination program leading into the spring and summer. They have to get this right.”
Editorial Board, USA Today
