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. 2023 Nov 3;15(11):2580. doi: 10.3390/pharmaceutics15112580

Table 7.

Dosing regimens (q12h, mg) for heart transplant recipients with CYP3A5 and CYP3A4 genotypes based on BW, hematocrit, and drug combination.

BW < 50 kg PM EM
Drug combination Hematocrit Hematocrit Hematocrit Hematocrit
(0.2–0.3) (0.3–0.4) (0.2–0.3) (0.3–0.4)
Without voriconazole 2.5 (92.5) * 1.8 (90.7) * 4.0 (94.8) * 2.8 (96.1) *
With voriconazole 1.0 (91.8) * 0.5 (92.4) * 2.0 (90.7) * 1.0 (94.5) *
BW = 50–80 kg PM EM
Drug combination Hematocrit
(0.2–0.3)
Hematocrit
(0.3–0.4)
Hematocrit
(0.2–0.3)
Hematocrit
(0.3–0.4)
Without voriconazole 3.0 (93.8) * 2.5 (96.3) * 4.5 (93.3) * 3.0 (95.7) *
With voriconazole 1.5 (92.9) * 1.0 (94.1) * 2.5 (90.5) * 1.5 (91.9) *
BW > 80 kg PM EM
Drug combination Hematocrit Hematocrit Hematocrit Hematocrit
(0.2–0.3) (0.3–0.4) (0.2–0.3) (0.3–0.4)
Without voriconazole 3.5 (93.2) * 2.5 (91.8) * 5.0 (95.3) * 3.2 (94.2) *
With voriconazole 1.5 (92.5) * 1.0 (94.4) * 2.5 (93.7) * 2.0 (94.0) *

* Percentage of trough concentrations within target concentrations during therapy; BW: bodyweight; EM: extensive metabolizers (CYP3A5*1*1 or *1*3 and CYP3A4*18B*18B or CYP3A4*1*18B); PM: poor metabolizers (CYP3A5*3*3 and CYP3A4*1*1).