2021
DOI: 10.1093/ofid/ofab656
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Short-Term Safety of Booster Immunization With BNT162b2 mRNA COVID-19 Vaccine in Healthcare Workers

Abstract: This study demonstrated good short-term safety profile after a third dose of BNT162b2 vaccine among HCWs. There were more frequent local reactions and less systemic reactions compared to the second dose. HCW's who reported reactions had higher pre-booster titer of anti-S1 antibodies compared to those reported no reactions.

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Cited by 12 publications
(12 citation statements)
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“…In line with data on the general population [ 32 ], the drop in antibody titers observed around the 6th month, following the second vaccine dose administration, raises some concerns on the potential waning of immunity. This aspect is particularly true in immunodepressed patients and supports the necessity of a third and even a fourth booster dose to ameliorate their safety profile [ 33 ].…”
Section: Resultsmentioning
confidence: 64%
“…In line with data on the general population [ 32 ], the drop in antibody titers observed around the 6th month, following the second vaccine dose administration, raises some concerns on the potential waning of immunity. This aspect is particularly true in immunodepressed patients and supports the necessity of a third and even a fourth booster dose to ameliorate their safety profile [ 33 ].…”
Section: Resultsmentioning
confidence: 64%
“…The more information that can be realized, the better it is for people to select the appropriate brand of vaccine [ 2 , 14 ]. According to an Israeli study, the third dose of BNT162b2 was linked to modest short-term local and systemic responses, which were more common in younger vaccinees [ 7 ]. Another study on primary series found that post-vaccination adverse outcomes in BNT162b2 and ChAdOx1 differed by gender [ 17 ].…”
Section: Discussionmentioning
confidence: 99%
“…The lack of post-vaccination surveillance and real-world data support made it difficult to select the most appropriate vaccine [ 3 ]. Although many countries had national or hospital-based self-reporting surveillance systems in place, such as the Vaccine Adverse Event Reporting System (VAERS) and Vaccine Safety Datalink (VAS) in the United States and the Yellow Card Scheme in the United Kingdom [ 4 , 5 ], only a few studies examined the AE of the mix-and-match booster method [ 6 , 7 ]. As more and more brands of the COVID-19 vaccine were introduced into clinical use, multiple combinations of primary boosters were presented.…”
Section: Introductionmentioning
confidence: 99%
“…Fever, headache, fatigue, and pain at the injection site were the most known adverse reactions to COVID-19 vaccines, and overall, most adverse reactions were mild and short-lived [22, 23]. Although very rare, there have been reports of serious adverse reactions.…”
Section: Discussionmentioning
confidence: 99%
“…Our results suggest that mRNA vaccines require booster vaccinations to induce adequate immunity, like inactivated vaccines such as the hepatitis B vaccine. Fever, headache, fatigue, and pain at the injection site were the most known adverse reactions to COVID-19 vaccines, and overall, most adverse reactions were mild and shortlived [22,23]. Although very rare, there have been reports of serious adverse reactions.…”
Section: Discussionmentioning
confidence: 99%