“…Increased hepatic enzyme levels (40 percent) and eosinophilia (25 percent) were the most common adverse effects, followed by elevated triglyceride levels (20 percent), leukocytosis (10 percent), and headache (5 percent). 21 The major pharmacokinetic drug interactions with the antifungal medications in the treatment of tinea capitis either involve factors affecting gastrointestinal absorption or drug metabolism. The azoles (ketoconazole, itraconazole, and fluconazole) inhibit cytochrome P-450 3A4 and 2C9, and thus impair the metabolism of drugs, leading to toxic concentrations of concurrendy administered drugs in some patients.…”