The Prevalence of Immediate Hypersensitivity Reactions to the BNT162b2 mRNA Vaccine against SARS-CoV-2: Data from the Vaccination Campaign in a Large Academic Hospital

Author:

Paoletti Giovanni12ORCID,Pepys Jack1ORCID,Bragato Maria1ORCID,Paoletti Sandro3,Piona Alessandra4,Messina Maria1,Racca Francesca1ORCID,Ferri Sebastian1ORCID,Nappi Emanuele1,Costanzo Giovanni1,Del Moro Lorenzo15,Puggioni Francesca1ORCID,Canonica Giorgio12,Azzolini Elena26,Heffler Enrico12ORCID

Affiliation:

1. Personalized Medicine, Asthma and Allergy, IRCCS Humanitas Research Hospital, Rozzano, 20089 Milan, Italy

2. Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, 20090 Milan, Italy

3. Primary Care Pediatrics, ASL, 09121 Cagliari, Italy

4. Allergy Service, Humanitas San Pio X Hospital, 20159 Milano, Italy

5. Department of Clinical and Experimental Medicine, University of Florence, 50134 Florence, Italy

6. Clinical Quality Department, IRCCS Humanitas Research Hospital, Rozzano, 20089 Milan, Italy

Abstract

The anti-SARS-CoV-2 vaccination has probably been the most effective tool for preventing the infection and negative outcomes of the COVID-19 disease, and therefore for interrupting the pandemic state. The first licensed SARS-CoV-2 vaccine was BNT162b2, an mRNA vaccine that has been widely used since the earliest stages of the global vaccination campaign. Since the beginning of the vaccination campaign, some cases of suspected allergic reactions to BNT162b2 have been described. Epidemiological data, however, have provided reassuring results of an extremely low prevalence of these hypersensitivity reactions to anti-SARS-CoV-2 vaccines. In this article, we describe the results of a survey carried out through the use of a questionnaire, administered to all the health personnel of our university hospital after the first two doses of the BNT162b2 vaccine, which investigated the development of adverse reactions after a vaccination. We analyzed the responses of 3112 subjects subjected to the first dose of the vaccine; among these, 1.8% developed symptoms compatible with allergic reactions and 0.9% with clinical manifestations of possible anaphylaxis. Only 10.3% of the subjects who had allergic reactions after the first injection experienced similar reactions after the second dose and none of them experienced anaphylaxis. In conclusion, the anti-SARS-CoV-2 vaccination is rarely associated with severe allergic reactions and the second dose of vaccine is safe for this group of patients.

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Drug Discovery,Pharmacology,Immunology

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