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Administration of recombinant human EPO (rhEPO) has been shown to be effective in the reduction of inflammation and activation of the healing process in a wide variety of preclinical models as well as in patients

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Although the FDA is not aware of any compounding or marketing of the 3 proposed categories for human use, they claim it will benefit compounders by reducing regulatory uncertainty.1 In the future, the FDA may include these categories of drugs for human use