“…[83] It has been demonstrated that various patient factors can influence the pharmacokinetic parameters of systemic tacrolimus, which include demographic characteristics, [84][85][86][87] hepatic dysfunction, [84,85,88] hepatitis C, renal function, time after transplant, age, donor characteristics, sex, race, hematocrit and albumin concentrations, diurnal variations, administration of food, corticosteroid dosage, diarrhea, ascites, short or absent small bowel jejunostomy, and intestinal P-glycoprotein as well as cytochrome P450 expression. [53] Orally administered tacrolimus is also used for treatment of rheumatoid arthritis, [89][90][91] moderate to severe psoriasis, [92,93] and inflammatory bowel disease, [94][95][96][97] often in combination with other therapeutics. Lower daily doses (1.5-3 mg day) than for transplant patients are used for these conditions, resulting in lower trough tacrolimus concentrations in serum ranging from 2 to 10 ng mL.…”