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COVID-19 vaccine shipments begin in the US
Boxes containing the Pfizer-BioNTech COVID-19 vaccine are prepared to be shipped at the Pfizer Global Supply Kalamazoomanufacturing plant in Portage, Michigan, yesterday. (Photo: AP)
COVID-19, News
December 14, 2020

COVID-19 vaccine shipments begin in the US

KALAMAZOO, Michigan (AP) — The first shipments of a COVID-19 vaccine for widespread use in the United States headed yesterday from Michigan to distribution centres across the country, with the first shots expected to be given in the coming week to health care workers and at nursing homes.

Shipments of the Pfizer vaccine will set in motion the biggest vaccination effort in American history at a critical juncture of the pandemic that has killed 1.6 million and sickened 71 million worldwide.

Initially, about three million doses were expected to be sent out, and the priority is health care workers and nursing home residents as infections, hospitalisations and deaths soar in the US. With numbers likely to get worse over the holidays, the vaccine is offering a bright spot in the fight against the pandemic that’s killed nearly 300,000 Americans.

Federal officials say the first shipments of Pfizer’s vaccine will be staggered, arriving in 145 distribution centres today, with an additional 425 sites getting shipments tomorrow, and the remaining 66 on Wednesday. The vaccine, co-developed by German partner BioNTech, is being doled out based on each state’s adult population.

Pennsylvania health care giant UPMC has chosen staff who are critical to operating its facilities as among those getting the first round of vaccinations, said Dr Graham Snyder, who led the centre’s vaccine task force.

“It’s very exciting. I will be thrilled, that moment when we administer our first dose,” Snyder said last Saturday. “That will clearly be a watershed moment for us.”

Snyder said the UPMC system estimates that half its employees are willing to get the vaccine as soon as it’s offered to them.

The vaccine is heading to hospitals and other sites that can store it at extremely low temperatures — about 94 degrees below zero. Pfizer is using containers with dry ice and GPS-enabled sensors to ensure each shipment stays colder than the weather in Antarctica.

Doses should be delivered to all vaccination sites identified by states, such as local pharmacies, within three weeks, federal officials said.

The 40-hospital Oschner Health System in Louisiana and Mississippi expects to receive more than 9,000 doses in the coming days, said Dr Sandra Kemmerly, medical director of hospital quality.

Employees approved for the first round are getting texts and e-mails directing them to schedule their initial injection, she said.

“I would say there’s enthusiasm,” Kemmerly said last Saturday. “There’s that thought that maybe they don’t have to be so afraid to come to work if they can be vaccinated and be immune.”

The roll out will ensure there is enough vaccine to give people the two doses needed for full protection against COVID-19. That means the Government is holding back three million doses to give those vaccinated in the first round a second shot a few weeks later.

The Food and Drug Administration (FDA) authorised emergency use of the vaccine last Friday, saying it is highly protective and presents no major safety issues. While US regulators worked for months to emphasise the rigour and independence of their review, they faced political pressure until the final stages.

Concerns that a shot was rushed out could undermine vaccination efforts in a country where some are sceptical about vaccines — some because of overall opposition to vaccines and others because of the quick time frame in which the virus vaccines were developed. Even some health care workers have said in surveys that they would forgo at least the first round of shots to see how things go.

The head of the FDA has repeatedly insisted that the agency’s decision was based on science, not politics, despite a White House threat to fire him if the vaccine wasn’t approved before last Saturday.

While the vaccine was determined to be safe, regulators in the UK are investigating several severe allergic reactions. The FDA’s instructions tell providers not to give it to those with a known history of severe allergic reactions to any of its ingredients.

Another vaccine by Moderna will be reviewed by an expert panel next week and soon afterward could be allowed for public use.

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