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The marketing narrative that PDA is a "legal alternative" to BPC-157 rests on the unsupported argument that the FDA's Category 2 classification does not cover arginate salt variants
Age Ageing 41 , 587594 (2012)
These animals were also subjected to the same environmental conditions and treatment protocols for a chronic 28-day administration study [2]
Five patients (6%) in the erlotinib group developed serious treatment-related adverse reactions, as opposed to 16 patients (20%) in the chemotherapy group 60 (Table 2)
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