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Oral reduced GSH 250 mg/day or oxidized GSSG 250 mg/day, 12 weeks, 3-arm RCT (n=60, women)

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Adverse events caused treatment discontinuation in 4.3%, 7.1%, 6.2%, and 2.6% of participants receiving 5-mg, 10-mg, 15-mg tirzepatide doses and placebo, respectively [49]

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