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It is produced without the manufacturing standards, sterility requirements, or potency documentation that a licensed pharmacy must maintain
Nov 2016;71(11):1052-1054
The infections found in CGD patients are primarily associated with a subset of catalase-positive microorganisms
To get a drug FDA approved, a company must conduct phase 1, 2 and 3 clinical trials proving safety and efficacy of the compound through a laborious, multi year and extremely costly process
The choice comes down to mechanism preference, regulatory comfort level, and individual health context - and the two can be used together without known adverse interaction
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