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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)

doi: 10.1002/psc.2420 [DOI] [PubMed] [Google Scholar] 208.Dathe M, Nikolenko H, Meyer J, Beyermann M, Bienert M

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