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Adverse Events FDA received an adverse event report on January 14, 2019, regarding seven patients in an outpatient clinic who received intravenous injections containing L-glutathione 200mg/mL compounded by a pharmacy using L-glutathione repackaged by Letco (lot number: 1810150050, expiration date: 6/17/2020)

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These in vitro mechanisms were recapitulated ex vivo, as observed by the strong correlations of ex vivo 15LO1 protein with intracellular GSH ( r = 0.68, P = 0.005) and GSH:GSSG ( r = 0.62, P = 0.014) in freshly brushed HAECs (Figure 3F)

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Consent for publication Written informed consent for publication of the study results and related data was obtained from the patients parents

doi: 10.3389/fpls.2016.01948 9 DaiX