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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)

Biomed Mater 18, 035004.CrossRefGoogle Scholar Ballatori, N, Krance, SM, Marchan, R, et al

Peng, C

"If you go that route, the smart move is to do it with a qualified provider, since dosing is not standardized and, while reactions are uncommon, it is a medical treatment, not a casual add-on." Are There Downsides to Taking Glutathione

PMID: 38873418 Simple diagnostic test using GH-releasing peptide-2

These injections are not approved by the FDA and are often unregulated