Additional file 2.

AViDD trial sensitivity analyses, weekly symptoms reported, and biochemical and safety data. This file includes summaries of intention-to-treat analyses versus sensitivity analyses (Table S1), frequency of reported symptoms based on weekly clinical monitoring (Table S2), biochemical adverse events (Table S3) and clinical serious adverse events (Table S4) at any time during follow-up, and biochemical and clinical data among newborns with clinical serious adverse events (birth to 1 month postnatal).

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Roth et al. Nutrition Journal 2013 12:47   doi:10.1186/1475-2891-12-47