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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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While alteration to the gut microbiota may potentially enhance the quality of life for children with these disorders, the therapeutic impact is expected to be less significant compared to diseases influenced by environmental factors