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Transient sensory symptoms among first-dose recipients of the BNT162b2 mRNA COVID-19 vaccine: A case-control study

•Evidence of transient sensory symptoms in recipients of BNT162b2 mRNA COVID-19 is scarce.•Sensory symptom frequency in first dose recipients of BNT162b2 who reported an AEFI is 3.4% (95% CI 3.1% to 3.8%).•Arms and face/neck are the most commonly affected sites (61% and 36.2%, respectively).•Healthc...

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Bibliographic Details
Published in:Vaccine 2021-11, Vol.39 (48), p.6975-6979
Main Authors: García-Grimshaw, Miguel, Ceballos-Liceaga, Santa Elizabeth, Michel-Chávez, Anaclara, García-Alanis, Mario, Cadena-Fernández, Arturo, Galnares-Olalde, Javier Andrés, Carbajal-Sandoval, Guillermo, Carrillo-García, Daniel Amado, Hernández-Valdivia, Noé, Hernández-Vanegas, Laura E., Saniger-Alba, María del Mar, Gutierrez-Romero, Alonso, Díaz-Ortega, José Luis, Reyes-Terán, Gustavo, López-Gatell, Hugo, Flores-Silva, Fernando Daniel, Cantú-Brito, Carlos, Chiquete, Erwin, Arauz, Antonio, Valdés-Ferrer, Sergio Iván
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Language:English
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Summary:•Evidence of transient sensory symptoms in recipients of BNT162b2 mRNA COVID-19 is scarce.•Sensory symptom frequency in first dose recipients of BNT162b2 who reported an AEFI is 3.4% (95% CI 3.1% to 3.8%).•Arms and face/neck are the most commonly affected sites (61% and 36.2%, respectively).•Healthcare workers have lower odds for reporting sensory symptoms (aOR 0.54; 95% CI 0.40–0.72;p 
ISSN:0264-410X
1873-2518
DOI:10.1016/j.vaccine.2021.10.058