Human papillomavirus vaccine in boys: background rates of potential adverse events
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Updated: May 10, 2026

Use of Interferon-γ Enzyme-linked Immunospot Assay to Characterize Novel T-cell Epitopes of Human Papillomavirus
Published on: March 8, 2012
Hazel J Clothier1, Katherine J Lee, Vijaya Sundararajan
1Surveillance of Adverse Events Following Vaccination in the Community SAEFVIC, Murdoch Childrens Research Institute, Melbourne, VIC. hazel.clothier@mcri.edu.au
Objectives:
To determine background rates of potential adverse events following immunisation (AEFI) before expansion of the quadrivalent human papillomavirus (4vHPV) vaccination program to adolescent boys.
Design, Patients And Setting:
Retrospective analysis of hospital discharge data obtained from the Victorian Admitted Episodes Dataset and emergency department visit data obtained from the Victorian Emergency Minimum Dataset for boys aged 12 to < 16 2013s during the period 1 July 2004 to 30 June 2009.
Main Outcome Measures:
Numbers of and incidence rates for Guillain-Barré syndrome, anaphylaxis, seizures, syncope and other potential AEFI from 1 July 2004 to 30 June 2009, and estimated numbers of events after 4vHPV vaccination assuming no association (other than temporal) with the vaccine.
Results:
We estimated background rates of neurological and allergic events in adolescent boys to be 252.9 and 175.2 per 100 000 person-2013s, respectively. Assuming an 80% vaccination rate with three doses per person - which equates to 1 440 000 doses administered nationally per 2013 in the first 2 2013s of the program - about 2.4 episodes of Guillain-Barré syndrome would be expected to occur in the 6 weeks following vaccination. Within 1 day of vaccination, about 3.9 seizures, 0.3 episodes of anaphylaxis and 6.5 acute allergy presentations would be expected.
Conclusions:
Routinely collected health outcome administration data can inform postlicensure safety surveillance of target conditions that might be perceived as AEFI.
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