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It is believed to be well absorbed after oral administration. Its absorption is best in an acidic environment and should not be given with H2 blockers or antacids.
Ketoconazole distributes into bile, saliva, urine, synovial fluid, and cerebral spinal fluid. Its highest levels are found in the liver, adrenals, and pituitary gland. Lesser levels are found in kidneys, lungs, bladder, bone marrow, and the mycocardium. It binds to plasma proteins and can cross the placental barrier in rats as well as in breast milk.
The drug is metabolized by the liver and excreted into the feces via bile.
Antacids, anticholinergics, H2 blockers may inhibit absorption of ketoconazole.
Mitotane not recommended to be used with ketoconazole in treating hyperadrenocorticism.
Ketoconazole and phenytoin may interfere with each others absorbtion.
Ketoconazole changes the disposition, and lengthens the duration of activity by methylprednisolone.
Ketoconazole increases the concentration of cisapride which can lead to ventricular arrhythmias. Do not use these drugs together.
Serum theophylline levels are decreased when used with ketoconazole.
Rifampin decreases ketoconazole levels; adjust dosage if using together.
GI: anorexia(poor or no appetite), diarrhea, anal pruritus(itching)
Other: increased liver enzymes, hepatotoxicity
Posted on June 23, 2003, 16:02,
Last updated on December 12, 2008, 15:48
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