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Headline Roundup March 23rd, 2021

Independent Board Says AstraZeneca Vaccine Announcement Relied on Old Information

Summary from the AllSides News Team

The National Institute of Allergy and Infectious Diseases (NIAID) said Tuesday that an independent board that reviews data from COVID-19 vaccine candidates is concerned about AstraZeneca's recent announcement of efficacy data from its vaccine trial. AstraZeneca issued a press release Monday saying its vaccine is 79% effective against symptomatic disease and 100% effective against severe disease and hospitalization. The review board reportedly wrote a letter to the company raising concerns about "outdated information" used in that announcement "which may have provided an incomplete view of the efficacy data." Several countries suspended use of AstraZeneca's vaccine last week amid concerns about blood clots, which health experts later dispelled; the Biden administration said last week it will send 2.5 million doses of the drug to Mexico and 1.5 million to Canada. The drug is not yet approved for use in the United States; AstraZeneca said Tuesday it intends to release results of a more recent analysis in the coming days. Coverage from all sides, especially some right-rated outlets, framed AstraZeneca's management of its vaccine trial in a negative light. Reports from left- and center-rated outlets highlighted data and testimonies from health experts suggesting the company's vaccine is ultimately safe despite concerns; right-rated outlets featured this information less prominently. Some voices from the left said the intense scrutiny around the drug represented "vaccine safety at work."

Featured Coverage of this Story

From the Center
New questions about AstraZeneca vaccine could derail its emergency use in US
New questions about AstraZeneca vaccine could derail its emergency use in US

The Hill

News

Late Monday evening, a U.S. public health agency expressed concern regarding the newly released clinical trial results from the pharmaceutical company AstraZeneca’s COVID-19 vaccine candidate.

Following the release of promising data showing high levels of efficacy in preventing a COVID-19 infection and severe outcomes, AstraZeneca officials confirmed they would be seeking the U.S. Food and Drug Administration’s (FDA) emergency use authorization.

This could be derailed as a public health oversight committee, the Data and Safety Monitoring Board (DSMB) said the clinical trials could have used outdated information in the trials,...

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From the Right
AstraZeneca Cherry-Picked Data, Misrepresented Vaccine’s Efficacy, Independent Medical Board Alleges
AstraZeneca Cherry-Picked Data, Misrepresented Vaccine’s Efficacy, Independent Medical Board Alleges

The Daily Caller

News

An independent panel of medical experts overseeing AstraZeneca’s coronavirus vaccine trial accused the pharmaceutical company of cherry-picking favorable data, The New York Times reported.

The Data and Safety Monitoring Board (DSMB) alleged that AstraZeneca misrepresented the results of its coronavirus vaccine trial when it announced Monday morning that the vaccine had 79% efficacy at preventing symptomatic coronavirus, according to the NYT. The panel wrote a sharply-worded letter to the British pharmaceutical company and U.S. health officials hours after the results were released, triggering the National Institute of Allergy and Infectious...

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Possible Paywall
From the Left
Trial review board raises concerns about AstraZeneca vaccine data
Trial review board raises concerns about AstraZeneca vaccine data

CNN Digital

News

In an unusual statement released early Tuesday, the National Institute of Allergy and Infectious Diseases said the independent board that reviews data from multiple Covid-19 vaccine candidates has raised concerns about AstraZeneca's announcement of efficacy data from its vaccine trial.

"The DSMB expressed concern that AstraZeneca may have included outdated information from that trial, which may have provided an incomplete view of the efficacy data," said the NIAID statement released early Tuesday.

"We urge the company to work with the DSMB to review the efficacy data and ensure the most...

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