Anaphylaxis is a rare side-effect of
COVID-19 vaccines. To (a) provide direct advice and reassurance to certain persons with a history of
anaphylaxis/complex
allergy, in addition to that available in national guidelines, and (b) to provide a medically supervised vaccination, a specialist regional
vaccine allergy clinic was established. The main objective was to determine if risk stratification through history can lead to safe
COVID-19 vaccination for maximum population coverage. A focused history was taken to establish
contraindications to giving
COVID-19 vaccines. People who reported a high-risk
allergy history were given a
vaccine not containing the
excipient thought to have directly caused previous
anaphylaxis. All
vaccines were monitored for 30 min after administration. A total of 206 people were vaccinated between 6 July 2021 and 31 August 2021;
Comirnaty (Pfizer-BioNTech) (n = 34), and Janssen (n = 172). In total, 78% were women. Ninety-two people (45%) reported a high-risk
allergy history. There were no cases of
anaphylaxis. Three people developed
urticaria and one of these also developed transient
tachycardia. One vaccinee developed a pseudoseizure. Two of 208 people (<1%) referred during this time declined vaccination based on personal preference, despite the assessment of low clinical risk. In our experience, all
vaccines with high-risk
allergy histories were administered Pfizer BioNTech or Janssen
Covid-19 vaccines uneventfully following screening based on
allergy-focussed history. Our data support that
drug allergy is not associated with a higher risk of
vaccine-related
anaphylaxis but may act to guide the administration of alternate
vaccines to people with
polyethylene glycol/
polysorbate 80/
trometamol allergies or
anaphylaxis after the first dose.