Specification | Description |
---|---|
Drug Class | Triazole antifungal |
Mechanism of Action | Inhibits fungal cytochrome P-450-dependent enzymes |
Route of Administration | Oral and intravenous |
Half-life | 6-8 hours |
Protein Binding | Approximately 58% |
Metabolism | Hepatic metabolism |
Excretion | Primarily through urine (mostly as metabolites) |
Dosage Forms | Tablets, intravenous solution |
Available Strengths | Tablets: 50 mg, 200 mg; IV: 200 mg in 20 mL vial |
Storage | Store at room temperature, protect from light |
Stability | Stable for up to 24 hours after reconstitution |
Common Side Effects | Visual disturbances, liver abnormalities, rash |
Contraindications | Known hypersensitivity to Voriconazole or related compounds |
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