The second category included substances considered too risky for compounding
The prescriber should also monitor the patient for any signs of adverse effects or interactions with other medications
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To further elucidate the therapeutic mechanisms underlying D-CuPs multivalent interactions, comprehensive proteomic analysis revealed two pivotal transcriptional regulators, the tumor suppressor protein p53 and histone deacetylase 7 (HDAC7) to be potential mechanistic targets
