Voriconazole and cell transporters
Voriconazole is an antifungal agent against species of Candida, Aspergillus, Scedosporium or Fusarium.
Its mechanism of action consists in the inhibition of the fungal enzyme 14-alpha-sterol demethylase, an essential enzyme in the biosynthesis of ergosterol, an essential compound for fungi.
Voriconazole is contraindicated in concomitance with: terfenadine, astemizole, cisapride, pimozide and quinidine due to the risk of prolongation of the QTc interval. Voriconazole is contraindicated in concomitance with rifampicin, carbamazepine and phenobarbital, high doses of ritonavir (≥ 400 mg 2 times/day), high doses of efavirenz (≥ 400 mg/day), ergot alkaloids due to risk of ergotism, sirolimus and hypericum.
Previous hypersensitivity to azole compounds.
Precautions should be taken when prescribing voriconazole in patients with acquired or congenital prolongation of the cardiac QT interval, cardiomyopathy (in particular with associated heart failure), sinus bradycardia, symptomatic arrhythmia, precautions in concomitance with QT prolongation. It is recommended before and during treatment to monitor and correct electrolyte alterations (hypokalemia, hypomagnesemia and hypocalcemia).
During treatment with voriconazole it is recommended to monitor liver function at the beginning and at least once a week during the first month of treatment and in case of alteration of the liver function tests during the entire duration of the treatment. If the treatment is prolonged, perform liver function tests once a month and consider suspension of treatment if there are signs of liver disease.
In patients with severe hepatic impairment, the risk/benefit should be assessed before prescribing voriconazole.
Avoid exposure to sunlight, voriconazol has been associated with photoxicity, pseudoporphyria and in prolonged treatments has been reported squamous cell carcinoma of the skin, with increased risk in children.
In cases of concomitance of treatment with other drugs, a risk/benefit assessment is recommended before prescribing voriconazole:
Ritonavir, phenytoin, rifabutin, methadone, short-acting opioids (alfentanil, fentanyl, sulfentanil) or long-acting opioids (oxycodone, hydrocodone), CYP3A4 substrates. Intensive and frequent adverse effects associated with opiates should be monitored and dosage adjustment considered. One should monitor adverse effects of voriconazole if used sequentially after fluconazole. On concomitant treatment with efavirenz, increase the maintenance dose of voriconazole to 400 mg/12 h and reduce the dose of efavirenz to 300 mg/24 h. Treatment with voriconazole produces a risk of increasing the levels of everolimus, thus concomitant intake is not recommended.
In children under 2 years old there are insufficient data on efficacy and safety in intravenous treatments.
Gastroenteritis, sinusitis, gingivitis.
Squamous cell carcinoma, agranulocytosis, pancytopenia, thrombocytopenia, anemia, hypersensitivity, peripheral edema, hypoglycemia, hypokalemia, hyponatremia, depression, hallucinations, anxiety, insomnia, agitation, confusional state, headache, convulsion, tremors, paresthesia, hypertonia, somnolence, syncope , dizziness and visual disturbance (blurred vision, chromatopsia, photophobia).
Retinal hemorrhage, supraventricular arrhythmia, tachycardia, bradycardia, hypotension, phlebitis, respiratory distress, acute respiratory distress syndrome, pulmonary edema, abdominal pain, nausea, vomiting, diarrhea, dyspepsia, constipation, cheilitis. Elevated liver function tests, jaundice, cholestatic jaundice, hepatitis. Eruption/rash, exfoliative dermatitis, maculopapular rash, pruritus, alopecia, erythema, back pain, acute renal failure, hematuria, pyrexia, chest pain, facial edema, asthenia, flu-like illness, chills and increases in creatinine levels.
Monitor the concentration of ciclosporin (it is recommended to reduce the dose by half) and tacrolimus (it is recommended to reduce the dose to one third).
Consider a dose adjustment of: statins metabolized by CYP3A4, benzodiazepines, omeprazole (it is recommended to reduce the dose by half).
Nausea and menstrual disorders in concomitance with oral contraceptives.
Control toxicity and/or loss of efficacy with non-nucleoside reverse transcriptase inhibitors (antiretrovirals)
Voriconazole increases the Cmin. and AUC (""Area Under the Curve"") of NSAIDs, monitor adverse effects and toxicity.
Voriconazole is incompatible with simultaneous administration of blood products and perfusion of concentrated electrolyte solutions, simultaneous perfusion in the same cannula with other intravenous drugs.
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Gene or region studied