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Currently, treatment is individualized predicated on clinical evaluation regarding the risk of rejection or poisoning led by trough focus tracking. Advances in immune tracking have identified prospective markers that will have price in comprehending calcineurin inhibitor pharmacodynamics. Integration among these markers has the prospective to complement therapeutic medication tracking. Current pharmacokinetic-pharmacodynamic (PK-PD) data is largely limited to correlation between the biomarker and tro
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