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The FDA identifies significant risks including lack of human safety data, potential for adverse immune reactions, and insufficient evidence regarding long-term effects, with the agency authorized to take enforcement action against compounding pharmacies that produce these substances for clinical applications

Before making treatment recommendations, providers review: This evaluation helps ensure that treatment decisions are individualized and medically appropriate

One orthopedic specialist wrote that regulatory agencies must crack down on practitioners and pharmacies that expose patients to unapproved peptides

10.1016/j.numecd.2009.02.009 Nutr

Life sciences , 54 5, PL63-8