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When considering authorizing the updated booster, the FDA said it looked at immune response data from adults who had received the original booster, which targeted the original omicron variant BA.1, as well data from a study comparing children who received the original booster and children who only received the primary series
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If they make an exception for one patient, they may feel pressured to do so for others, leading to a system where ad-hoc changes become the norm
