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FDA received another adverse event report on February 4, 2019, associated with an intravenous injection of a drug containing L-glutathione 200mg/mL compounded by a different pharmacy that also used L-glutathione repackaged by Letco (lot number: 1808030045, expiration date: 6/17/2020)

doi:10.1016/S0003-2697(03)00143-X

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Identification of glutathione-overproducing mutants via acrolein resistance A genetically diverse S

Once inside the cell, endogenous enzymes readily convert glutathione reduced ethyl ester into reduced glutathione (Levy et al, 1993)