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Looking specifically at the Phase 3 trial data, only 1 of the 201 patients in the initial trial experienced injection site cellulitis, and 2 others of a total of 412 participants have experienced injection site cellulitis in the ongoing open-label long-term safety study.15 Possible explanations that may have predisposed our patient to an injection site reaction may have included improper injection of the medication, as adverse reactions are more likely to occur with intradermal or intramuscular injection.3 Both of these considerations were difficult to reconcile given the delayed onset from the injection

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