2021
DOI: 10.2105/ajph.2020.306036
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Communicating Effectively About Emergency Use Authorization and Vaccines in the COVID-19 Pandemic

Abstract: The Emergency Use Authorization (EUA) mechanism is central to the US response to coronavirus disease 2019 (COVID-19). It allows the US Food and Drug Administration (FDA) to respond quickly to novel threats by approving a new drug, device, or diagnostic procedure or expanding off-label use of an existing drug through an accelerated approval process.1 To obtain authorization, evidence must support that a drug or product “‘may be effective’ to prevent, diagnose, or treat serious or life-threatening diseases or co… Show more

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Cited by 50 publications
(43 citation statements)
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“…In summary, our findings echo the call for restoring trust in the healthcare system, scientists, and biomedical industries and highlight the urgency to dispel misinformation about COVID-19 vaccines in social media 38 . Effective strategies are needed to improve trust in pharmaceutical companies and government regarding vaccine communication and encourage these entities to partner with sources already trusted by the public.…”
Section: Discussionsupporting
confidence: 71%
“…In summary, our findings echo the call for restoring trust in the healthcare system, scientists, and biomedical industries and highlight the urgency to dispel misinformation about COVID-19 vaccines in social media 38 . Effective strategies are needed to improve trust in pharmaceutical companies and government regarding vaccine communication and encourage these entities to partner with sources already trusted by the public.…”
Section: Discussionsupporting
confidence: 71%
“…For example, the two vaccines from Pfizer-BioNTech and Moderna have been approved by the Food and Drug Administration (FDA) for emergency use, and both of them use messenger RNA (mRNA) for viral protein expression. 21 Several other leading COVID-19 vaccines (i.e., Oxford-AstraZeneca, Johnson & Johnson, CanSino) are made from segments of viral DNA, which is packaged inside the adenovirus for delivery into host cells. Recently, a similar adenovirus-based vaccine has been approved for Ebola.…”
Section: Reviewmentioning
confidence: 99%
“…Many public health commentators and researchers have called for transparent communication of COVID-19 vaccine information, including the efficacy and side effects reported from clinical trials, to improve vaccine uptake (Cohen et al, 2020; Nature, 2020; Quinn et al, 2021). Some, for example, Rzymski et al (2021), think that such information may change individuals’ vaccine beliefs: “The general public must be given access to the pivotal information on the authorized vaccines, and that their approval is based on the evidenced benefits that outweigh the potential risks of vaccine administration” (p. 3).…”
Section: Transparent Communication Of Vaccine Risks and Benefitsmentioning
confidence: 99%