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10.1126/sciimmunol.aao6923 182 MamontovaA.Sguret-MacS.EspositoB.ChanialeC.BoulyM.Delhaye-BouchaudN.et al
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
Epidemiology of neuropathic pain and its impact on quality of life
After April 22, that label is gone
