Of these 290 (61%) parents or carers completed the Vaxtracker online survey at day 3 following Paclitaxel research buy the first dose of IIV with 134 (47%) of those went on to complete the final survey at day 43 (Fig. 3). Most respondents to the online survey were aged between 5 years and 9 years 11 months (55%), 32% were aged between 2 and 5 years and 12% aged less than 2 years.

53% of respondents were males (n = 154). The mean number of days from sending the web survey link to completion of the survey dispatched on day 3 was 3.33 days (n = 290). The mean number of days from sending web survey link to completion of the final 42 day survey was 2.01 days (n = 120). Survey completion rates were highest when both email and mobile phone contact details were provided (n = 35, 74%) compared

to email (n = 135, DAPT molecular weight 58%) or mobile phone (n = 120, 60%) alone. Among the 477 participants, Vaxigrip (Sanofi) (n = 334) was the most commonly administered IIV, followed by Fluarix (GlaxoSmithKline) (n = 78), Influvac (Abbott) (n = 59), Vaxigrip Junior (Sanofi) (n = 4) and Agrippal (Novartis) (n = 2). Eighteen percent of respondents in the day three survey (52/290) reported any reaction following dose 1 across all IIV brands, three of whom reported receipt of another vaccine within one week of IIV administration. Over-all 8% of respondents (23/290) experienced a local reaction and 3% (8/290) reported fever. When considering specific IIV brands, Vaxtracker found a higher rate of all reported reactions following Vaxigrip/Vaxigrip jnr (21.5% (95% CI: 16.0–27.0%); n = 46/214) compared to all the other inactivated vaccine brands administered to participants (7.9% (95% CI: 1.8–14.0%); already n = 6/76, p = 0.0079) ( Table 1). However for fever there was no significant difference between Vaxigrip/Vaxigrip jnr (2.8% (95% CI: 0.6–5.0%); n = 6/214) and the other brands of IIV (2.6% (95% CI: 0.0–6.2%); n = 2/76, p = 0.9270). Participants who had received an IIV in the previous year also appeared to have

a higher rate of reactions than participants who did not (25.8% versus13.2% respectively). The odds of having a reaction for those who had IIV last year compared to those who did not is 1.95 (p = 0.036) when controlling for vaccine type, gender and age. Of the 134 respondents who completed the final survey, three (2.2%) reported a hospitalisation in the 42 day period following vaccination which triggered an email alert and clinical review on all three occasions. However, on clinical review each hospitalisation episode was determined to be unrelated to vaccination (two asthmatic children had experienced asthma attacks and one child had suffered a fracture following an accident). The Vaxtracker surveillance system found an intriguing difference in adverse event reaction rates between influenza vaccine brands in this cohort of children.