Indications & Dose:
To treat invasive aspergillosis to treat serious fungal infection caused by Scedosporium apiospermum and Fusarium species including Fusarium solani in papients intolerant of or refractory to other therapy.
Adult and Children over 12 years old overin g 40kg.: 200mg every 12 hours, increased to 300mg every 12 hours as needed and taken at least 1 hour bbefore or after meal.
]To treat Candidemia in nonneuropenic patients and other deep tissue disseminated Candia infections involving the abdomen kidney baldder wall, skin or a wound.
Adult ( Maintainance).: 200mg every 12 hours, every 12 hours taken at least 1 hour bbefore or after meal.
To treat iOesophageal candidiasis.
Adult.: 200mg every 12 hours, every 12 hours taken at least 1 hour bbefore or after meal for at least 14 days after signs and symptoms resolve.
Contraindications:
Coadministration with long-acting barbiturates, carbamazepine, CYP3A4 substrates (astemizole, cisapride, pimozide, quinidine, or terfenadine), efavirenz, ergot alkaloids, rifabutin, rifampin, ritonavir, sirolimus, or St. John’s wort; hypersensitivity to voriconazole or its components; galactose intolerance, glucose-galactose malabsorption, or Lapp lactase deficiency (oral form only contains lactose)
Side Effects:
Cautions:
Precautions:
Interaction:
DRUGS
alfentanil: Increased plasma alfentanil level and increased risk of adverse reactions benzodiazepines: Possibly prolonged sedative effect of benzodiazepines calcium channel blackers; HMG-CoA reduc-tase inhibitors, such as lovastatin; omepra-zole; sirolimus: Possibly increased plasma levels of these drugs, leading to increased risk of adverse reactions and toxicity carbamazepine, longacting barbiturates, phenytoin, rifampin: Decreased plasma voriconazole concentration coumarin,
warfarin: Possibly increased PTT cyclosporine, sirolimus, tacrolimus: Increased serum concentrations of these drugs and risk of toxicity, especially nephrotoxicity CYP3A4 substrates (astemizole, cisapride, pimozide, quinidine, terfenadine): Increased plasma levels of these drugs, which may lead to prolonged QT interval and, rarely, torsades de pointes
ergot alkaloids (ergotamine, dihydroergota-mine): May increase plasma level of ergot alkaloids, leading to ergotism fluconazole, oral contraceptives: Increased plasma voriconazole level and risk of toxicity HIVprotease inhibitors (amprenavir, nelfinavir, ritonavir, saquinavir), non-nucleoside reverse transcriptase inhibitors (delavirdine, efavirenz): Possibly inhibited metabolism of these drugs and voriconazole methadone: Increased plasma level of methadone, possibly leading to toxicity, including QT-interval prolongation oral
contraceptives: Increased plasma voriconazole level and risk of toxicity rifabutin: Increased rifabutin plasma level; decreased voriconazole plasma level St. John’s wort: Decreased plasma voriconazole level sulfonylureas: Possibly increased plasma level of sulfonylureas and increased risk of hypoglycemia
vinca alkaloids: Possibly increased risk of neurotoxicity
Warnings:
Adverse Effects:
CNS: Chills, dizziness, fever, hallucinations, headache
CV: Chest pain, hypertension, hypotension, peripheral edema, tachycardia, vasodilation
EENT: Abnormal or blurred vision, altered or enhanced visual perception, change in color perception, chromatopsia, dry mouth, eye hemorrhage, photophobia, visual disturbances
GI: Abdominal pain, diarrhea, elevated liver function test results, nausea, pancreatitis, vomiting
GU: Abnormal kidney function, acute renal failure, elevated serum creatinine level
HEME: Anemia, leukopenia, pancytopenia, thrombocytopenia
MS: Fluorosis, periostitis, skeletal pain
RESP: Respiratory disorders
SKIN: Cholestatic jaundice, erythema multiforme, jaundice, maculopapular rash, photosensitivity, pruritus, rash, Stevens-Johnson syndrome, toxic epidermal necrolysis
Other: Anaphylaxis (I.V. form), elevated alkaline phosphatase, hypokalemia, hypomagnesemia, sepsis
Lactations:
Special Precautions:
Counselling:
Side Effects Or Adverse Reactions:
Patient And Carer Advice:
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