2021
DOI: 10.1093/ajhp/zxab274
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Consequences of rush to emergency use authorization of bamlanivimab

Abstract: Disclaimer In an effort to expedite the publication of articles related to the COVID-19 pandemic, AJHP is posting these manuscripts online as soon as possible after acceptance. Accepted manuscripts have been peer-reviewed and copyedited, but are posted online before technical formatting and author proofing. These manuscripts are not the final version of record and will be replaced with the final article (formatted per AJHP style and proofed by the authors) at a later time.

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“…While the FDA’s decision to allow early access to COVID-19 vaccines and other treatments unquestionably saved lives, similar to drugs approved with a BTD, not all EUA-approved agents have been without controversy. Even before bamlanivimab’s EUA was revoked due to ineffectiveness against variants, concerns were raised about its questionable efficacy and incomplete safety profile [ 27 ].…”
Section: Discussionmentioning
confidence: 99%
“…While the FDA’s decision to allow early access to COVID-19 vaccines and other treatments unquestionably saved lives, similar to drugs approved with a BTD, not all EUA-approved agents have been without controversy. Even before bamlanivimab’s EUA was revoked due to ineffectiveness against variants, concerns were raised about its questionable efficacy and incomplete safety profile [ 27 ].…”
Section: Discussionmentioning
confidence: 99%