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In contrast, NAC 900 mg TID reduced FEV 1 decline (by 150 mL) versus placebo over 24 weeks, though primary endpoints were unmet due to underpowering (108)
People are signing the paperwork that says they understand the risks, and that removes the suppliers liability, explains Taylor
The mechanisms and potential therapeutic applications described remain under investigation and are not established for routine clinical use
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Patients who unknowingly receive unapproved formulations may face challenges if complications arise, including lack of liability recourse, absence of pharmacologic data, and difficulty receiving support from traditional pharmacies or insurers
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