Management of BNT162b2 mRNA COVID-19 vaccine in children aged 5-11 years with allergies, asthma, and immunodeficiency: consensus of the Italian Society of Pediatric Allergy and Immunology (SIAIP)

Ital J Pediatr. 2022 May 16;48(1):76. doi: 10.1186/s13052-022-01272-z.

Abstract

BNT162b2 vaccine, developed by BioNTech and Pfizer ha recently approved for use in children aged 5 to 11 years. Recent data show evidence of safety on the administration and serious adverse events have been rarely reported. However, allergic systemic reactions could occur. In some cases, a correct allergic evaluation allows identifying patients at risk of developing an anaphylactic reaction. Risk assessment of allergic reactions to COVID-19 vaccines is useful to limit contraindications to vaccination and help to safely vaccinate people supposed to be at risk of allergic reactions.

Keywords: Adverse event; Allergy; BNT162b2; COVID-19; Children; Pfizer BioNtech; SARS-CoV-2; Side effect; Vaccine; mRNA vaccine.

Publication types

  • Review

MeSH terms

  • Anaphylaxis*
  • Asthma*
  • BNT162 Vaccine
  • COVID-19 Vaccines / adverse effects
  • COVID-19* / epidemiology
  • COVID-19* / prevention & control
  • Child
  • Consensus
  • Humans
  • RNA, Messenger
  • SARS-CoV-2

Substances

  • COVID-19 Vaccines
  • RNA, Messenger
  • BNT162 Vaccine