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Increase to 0.5 mg weekly for the next 4 weeks

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One study found that 32% of patients receiving IV glutathione experienced adverse events, including liver dysfunction and one case of anaphylaxis.[8] The FDA has issued warnings about contaminated IV glutathione causing hospitalizations.[9] Theres no long-term safety data for ongoing IV use

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However, when there is an explicit need for sulfonamide antibiotic therapy, including anticipated immunosuppression due to a future organ transplant, 10 delabeling via DOC can be performed for both immunocompromised and immunocompetent patients categorized as low risk