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To the Author or anyone else that has a reference for this statement?: The exception to this rule is the single preparation of the sub-Q or IM dose that exceeds the volume safely injected at a single site

2 , 3 Conclusion These adverse events were consistent with reactions patients experience with excessive levels of endotoxin, and FDAs testing confirmed higher levels of endotoxin than is appropriate based on the dose of L-glutathione received intravenously