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| (flew-KOE-nuh-zole) |
| Diflucan |
| Class: Anti-infective/Antifungal |
Action Interferes with the formation of fungal cell membrane, causing leakage of cellular contents and cell death.
Indications Oropharyngeal and esophageal candidiasis; vaginal candidiasis; prevention of candidiasis in bone marrow transplant; cryptococcal meningitis.
Contraindications Standard considerations.
Oropharyngeal or esophageal candidiasis
ADULTS: PO/IV 200 mg first day, followed by 100 mg qd thereafter for minimum of 2 wk for oropharyngeal candidiasis or 3 wk for esophageal candidiasis. CHILDREN: PO/IV 6 mg/kg on first day, followed by 3 mg/kg qd thereafter for minimum of 2 wk for oropharyngeal candidiasis or 3 wk (at least 2 weeks after symptom resolution) for esophageal candidiasis.
Vaginal candidiasis
ADULTS: PO 150 mg single dose.
Prevention of candidiasis in bone marrow transplant
ADULTS: PO/IV 400 mg once daily; in patients with anticipated severe granulocytopenia (< 500 neutrophils/mm3) start fluconazole several days before anticipated onset and continue 7 days after neutrophil count rises > 1000 cells/mm3.
Cryptococcal meningitis
ADULTS: PO/IV 400 mg first day, followed by 200 mg qd thereafter (400 mg may be used) for 10 to 12 wk after CSF culture is negative for initial meningitis; 200 mg qd for suppression of relapse of cryptococcal meningitis.
Candidemia and disseminated candida infections
CHILDREN: PO/IV 6 to 12 mg/kg/day.
Cryptococcal meningitis–12 mg/kg on first day, followed by 6 mg/kg/day (or 12 mg/kg/day based on medical judgment of patient’s response). Recommended duration is 10 to 12 weeks after CSF becomes culture negative.
Suppression of relapse in AIDS patients– 6 mg/kg/day. NEONATES: Experience is limited to pharmacokinetic studies in premature newborns. Prolonged half-life has been noted. These children, in the first 2 wk of life, should receive the same mg/kg dosage as other children, but administered every 72 hr. After the first 2 wk, dose once daily.
Anticoagulants (eg, warfarin): Anticoagulant effect may be increased. Alfentanil, benzodiazepines (eg, midazolam), buspirone, corticosteroids (eg, prednisone), nisoldipine, tacrolimus, vinca alkaloids (eg, vincristine): Levels may be elevated by fluconazole, increasing the risk of side effects and toxicity. Cyclosporine: Increased cyclosporine concentrations. Hydantoins (eg, phenytoin): Increased hydantoin levels. Rifamycins (eg, rifampin): Fluconazole plasma levels may be reduced, decreasing therapeutic effects.
Lab Test Interferences Elevated transaminase levels. Coumadin: Increased PT may occur in patient receiving warfarin.
CNS: Headache; seizures. DERM: Rash, exfoliative skin disorder. GI: Nausea; vomiting; abdominal pain; diarrhea. HEMA: Leukopenia; thrombocytopenia. HEPA: Hepatic reactions, including abnormal liver function test results, hepatitis, cholestasis, hepatic failure.
Pregnancy: Category C. Lactation: Excreted in breast milk. Children: Efficacy not established; some patients 3 to 13 yr have been treated safely with 3 to 6 mg/kg/day. Anaphylaxis: Has occurred rarely. Dermatologic changes: Exfoliative skin disorders have been reported. Hepatic injury: Patients with abnormal liver function test results should be monitored for development of more severe hepatic injury. Immunocompromised patients: To prevent relapse, patients with AIDS and cryptococcal meningitis usually require maintenance therapy. Renal impairment: Dosage reduction based on creatinine clearance may be necessary.
| PATIENT CARE CONSIDERATIONS |
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