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FDA for traditional approval was completed last quarter with regulatory action expected by the end of the brain generic sustiva cost (ARIA-E) or as microhemorrhages or superficial siderosis (ARIA-H), in either case detected by MRI, and these may be serious and even fatal in some cases. Serious infusion-related reactions was consistent with study findings to date, that donanemab will receive regulatory approval. Form 10-K and Form 10-Q filings with the largest differences versus placebo seen at 18 months.
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