Skip to main content
. Author manuscript; available in PMC: 2016 Jun 16.
Published in final edited form as: Curr Treat Options Neurol. 2012 Jun;14(3):241–255. doi: 10.1007/s11940-012-0172-y
Standard dosage Aspergillosis: initial loading dose 6 mg/kg IV every 12 h for 2 doses, followed by 4 mg/kg IV every 12 h; may switch to oral dosing with 200 mg every 12 h as tolerated. May require treatment for 1 year. CNS candidiasis: may treat initially with amphotericin B followed by oral voriconazole as maintenance therapy.
Contraindications Concomitant use of carbamazepine, CYP3A4 substrates (terfenadine, astemizole, cisapride, pimozide, or quinidine), ergot alkaloids, long-acting barbiturates, rifabutin, rifampin, sirolimus, or St. John’s wort. Hypersensitivity to the drug.
Major side effects Visual disturbance (21 %), hallucinations (2.4 % to 16.6 %), rash (7 %). Hepatitis, pancreatitis, toxic encephalopathy and prolonged QT interval are rare.
Major drug interactions Drugs that induce liver enzymes can reduce plasma concentrations of voriconazole. Drugs with cardiac effects should be monitored closely. It may displace protein-bound drugs such as fosphenytoin to increase their concentration.
Special points It is the drug of choice for aspergillosis.