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All adverse events wereassessed and managed per KCH standard clinical practice, documented, followed up, and treated until resolution or stabilization.
All serious adverse events eAppendix 1 in Supplement 1 were reported for re- view within 24 hours.
The statistical analysis plan is provided in eAppendix 2 in Supplement 1.
A relative noninferiority marginof 1. This noninferiority margin was selected after extensive discus- sions among the investigators including A. I am also still very poorly, its cheaper than therapy.
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Methods The primary objective of this prospective, double-blind, 2-arm, randomized controlled noninferiority trial was to investigate whether treatment with placebo in HIV-uninfected children aged 2 to 59 months primary outcome of treatment failure TF by malaria-endemic region of Malawi was null hypoth- esis substantively less effective than 3 daysof hypothesis.
Given the paucity of such data from Africa, there is a critical need for African-specific research in malaria-endemic settings to establish need for antibiotic treat- ment of fast-breathing.