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Safety of COVID-19 Vaccines among People with History of Allergy: A European Active Surveillance Study.
Luxi, Nicoletta; Ciccimarra, Francesco; Bellitto, Chiara; Raethke, Monika; van Hunsel, Florence; Lieber, Thomas; Mulder, Erik; L'Abbate, Luca; Marques, Francisco Batel; Furci, Fabiana; Farcas, Andreea; Giele-Eshuis, Janneke; Morton, Kathryn; Sonderlichová, Simona; Thurin, Nicolas H; Villalobos, Felipe; Riefolo, Fabio; Sturkenboom, Miriam C; Trifirò, Gianluca.
Afiliación
  • Luxi N; Department of Medicine, University of Verona, 37134 Verona, Italy.
  • Ciccimarra F; Department of Diagnostics and Public Health, University of Verona, 37134 Verona, Italy.
  • Bellitto C; Department of Diagnostics and Public Health, University of Verona, 37134 Verona, Italy.
  • Raethke M; Netherlands Pharmacovigilance Centre Lareb, Goudsbloemvallei 7, 5237 MH 's-Hertogenbosch, The Netherlands.
  • van Hunsel F; Netherlands Pharmacovigilance Centre Lareb, Goudsbloemvallei 7, 5237 MH 's-Hertogenbosch, The Netherlands.
  • Lieber T; Department of PharmacoTherapy, Epidemiology & Economics, Groningen Research Institute of Pharmacy (GRIP), University of Groningen, 9712 Groningen, The Netherlands.
  • Mulder E; Netherlands Pharmacovigilance Centre Lareb, Goudsbloemvallei 7, 5237 MH 's-Hertogenbosch, The Netherlands.
  • L'Abbate L; Netherlands Pharmacovigilance Centre Lareb, Goudsbloemvallei 7, 5237 MH 's-Hertogenbosch, The Netherlands.
  • Marques FB; Department of Diagnostics and Public Health, University of Verona, 37134 Verona, Italy.
  • Furci F; Laboratory of Social Pharmacy and Public Health, School of Pharmacy, University of Coimbra, 3000-548 Coimbra, Portugal.
  • Farcas A; Provincial Healthcare Unit, Section of Allergy, 89900 Vibo Valentia, Italy.
  • Giele-Eshuis J; Pharmacovigilance Research Center, Iuliu Hatieganu University of Medicine and Pharmacy, 400347 Cluj-Napoca, Romania.
  • Morton K; Department of Data Science and Biostatistics, Julius Global Health, University Medical Centre Utrecht, 3584 Utrecht, The Netherlands.
  • Sonderlichová S; Drug Safety Research Unit, Southampton SO31 1AA, UK.
  • Thurin NH; University of Portsmouth, Portsmouth PO1 2UP, UK.
  • Villalobos F; Faculty of Medicine, SLOVACRIN, Pavol Jozef Safárik University in Kosice, 040 01 Kosice, Slovakia.
  • Riefolo F; University of Bordeaux, INSERM CIC-P 1401, Bordeaux PharmacoEpi, 146 rue Léo Saignat, 33076 Bordeaux, France.
  • Sturkenboom MC; Fundació Institut Universitari per a la Recerca a l'Atenció Primària de Salut Jordi Gol i Gurina (IDIAPJGol), 08007 Barcelona, Spain.
  • Trifirò G; Teamit Institute, Partnerships, Barcelona Health Hub, 08025 Barcelona, Spain.
Vaccines (Basel) ; 12(9)2024 Sep 17.
Article en En | MEDLINE | ID: mdl-39340089
ABSTRACT

Background:

Conventional vaccines rarely cause severe allergic reactions. However, the rapid development and approval of COVID-19 vaccines left limited initial data on their adverse reactions, particularly in individuals with a history of allergy. The aim of this study was to assess and compare the safety profile of different doses and brands of COVID-19 vaccines in subjects with a history of allergy vs. those without a history of allergy.

Methods:

From February 2021 to February 2023, a web-based prospective study gathered vaccinee-reported outcomes using electronic questionnaires across eleven European countries. Baseline and up to six follow-up questionnaires captured data on vaccinee demographics, as well as both solicited and unsolicited adverse reactions.

Results:

Overall, 3476 vaccinees with a history of allergy were matched with 13,872 vaccinees from the general population at the first vaccination cycle and were included in the analysis. A total of 825 vaccinees with a history of allergy who had received a booster dose, matched to 3297 vaccinees from the general population, were included in the analysis. Higher rates of ADRs occurred after the first vaccination cycle compared to after the booster dose (64-91% vs. 56-79%). However, most reported ADRs were solicited and not serious, and no case of anaphylaxis was reported. Women and vaccinees with a history of allergy reported ADRs more frequently than men and the matched controls, respectively. Compared to other COVID-19 vaccines, a higher proportion of vaccinees experiencing at least one ADR following their first vaccination cycle was observed with Comirnaty and Vaxzevria. Statistically significant differences were observed among the study cohorts for median TTO after the second dose, and for median TTR following the first vaccination cycle and booster dose (p < 0.001).

Conclusions:

Typically, any drug or vaccine use carries a risk of severe allergic reactions, yet the benefits of vaccination generally outweigh these potential risks, as shown with the COVID-19 vaccines.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Vaccines (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Vaccines (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Italia
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