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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

Piraud M, Vianey-Saban C, Petritis K, Elfakir C, Steghens J-P, Morla A, et al

[DOI] [PubMed] [Google Scholar] Isopi E., Mattoscio D., Codagnone M., Mari V.C., Lamolinara A., Patruno S., DAurora M., Cianci E., Nespoli A., Franchi S., Gatta V., Dubourdeau M., Moretti P., Di Sabatino M., Iezzi M., Romano M., Recchiuti A