It is the second such jab after Moderna's Spikevax to be allowed for inoculating those in the age group.
In making the decision, HSA consulted experts from its medicines advisory committee and panel of infectious diseases experts. The clinical data was based on an ongoing Phase 2/3 study conducted by Pfizer, involving about 1,800 participants aged 6 months through 4 years, according to HSA. Local real-world data in children aged five to 11 had shown that vaccine effectiveness against the Omicron subvariants was around 40 per cent for symptomatic disease and remained high at more than 80 per cent for protection against COVID-related hospitalisations for children receiving two doses of Pfizer vaccines.
"These reactions are generally associated with vaccinations and expected as part of the body’s natural response to build immunity against COVID-19. They usually resolve on their own within a few days," said HSA.
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