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These versions may be compounded by pharmacies when approved drugs are unavailable, but compounded drugs are not reviewed by the FDA for safety, effectiveness, or quality before being marketed
The incidence of severe hypoglycemia in: Adult and pediatric patients with type 1 diabetes mellitus who received subcutaneous NOVOLOG was 17% at 24 weeks and 6% at 24 weeks, respectively [see Clinical Studies (14)]
doi:10.1016/j.amjms.2025.07.006 Alharbi SH, et al
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