Vorix (Voriconazaole) 200mg Inection
Voriconazole 200 mg injection is used to treat serious fungal infections in the body, including:
- Invasive aspergillosis – a type of lung infection caused by Aspergillus fungi
- Candidemia in non-neutropenic patients and other deep tissue Candida infections
- Serious infections due to Fusarium species and Scedosporium apiospermum
The recommended dosing for voriconazole 200 mg injection is:
- Loading dose: 6 mg/kg IV every 12 hours on Day 1
- Maintenance dose: 4 mg/kg IV every 12 hours
IV therapy should continue for at least 7 days. Once the patient improves clinically and can tolerate oral medication, the oral tablet or suspension formulation may be used to complete treatment.Voriconazole is contraindicated in patients with known hypersensitivity to the drug or its ingredients. It also interacts with certain medications like rifampin, carbamazepine, long-acting barbiturates, and St. John’s wort, so concomitant use should be avoided.Patients should be monitored for development of abnormal renal function, as voriconazole can cause acute renal failure in some cases. Serum creatinine levels should be closely monitored, especially in those with moderate to severe renal impairment (creatinine clearance <50 mL/min).
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Description
Voriconazole 200 mg injection is used to treat serious fungal infections in the body, including:
- Invasive aspergillosis – a type of lung infection caused by Aspergillus fungi
- Candidemia in non-neutropenic patients and other deep tissue Candida infections
- Serious infections due to Fusarium species and Scedosporium apiospermum
The recommended dosing for voriconazole 200 mg injection is:
- Loading dose: 6 mg/kg IV every 12 hours on Day 1
- Maintenance dose: 4 mg/kg IV every 12 hours
IV therapy should continue for at least 7 days. Once the patient improves clinically and can tolerate oral medication, the oral tablet or suspension formulation may be used to complete treatment.Voriconazole is contraindicated in patients with known hypersensitivity to the drug or its ingredients. It also interacts with certain medications like rifampin, carbamazepine, long-acting barbiturates, and St. John’s wort, so concomitant use should be avoided.Patients should be monitored for development of abnormal renal function, as voriconazole can cause acute renal failure in some cases. Serum creatinine levels should be closely monitored, especially in those with moderate to severe renal impairment (creatinine clearance <50 mL/min).
Indications
- Invasive aspergillosis
- Candidemia in non-neutropenic patients and other deep tissue Candida infections
- Serious infections due to Fusarium species and Scedosporium apiospermum
Dosing
- Loading dose: 6 mg/kg IV every 12 hours on Day 1
- Maintenance dose: 4 mg/kg IV every 12 hours
- IV therapy should continue for at least 7 days
Contraindications
- Hypersensitivity to voriconazole or its ingredients
- Concomitant use with certain medications like rifampin, carbamazepine, long-acting barbiturates, and St. John’s wort
Monitoring
- Monitor renal function, especially in patients with moderate to severe renal impairment (creatinine clearance <50 mL/min)
- Closely monitor serum creatinine levels
Key Benefits of Voriconazole 200 mg Injection
- Treats serious fungal infections caused by Aspergillus, Candida, Scedosporium, and Fusarium species
- Effective in patients intolerant of or refractory to other antifungal therapies
- Rapid absorption with high oral bioavailability of 96%
- Achieves plasma concentrations close to steady state within the first 24 hours of dosing with loading dose regimen
Key Ingredients
- Active ingredient: Voriconazole 200 mg per vial
- Excipients: 221 mg sodium and 3,200 mg cyclodextrin per vial
The injection requires reconstitution to 10 mg/mL and subsequent dilution to 5 mg/mL or less prior to intravenous infusion over 1 to 3 hours.
Mechanism of Action of Voriconazole
The primary mode of action of voriconazole is the inhibition of fungal cytochrome P-450-mediated 14α-lanosterol demethylation, an essential step in ergosterol biosynthesis.Voriconazole is more selective than some other azole drugs for fungal cytochrome P-450 enzyme systems compared to various mammalian cytochrome P-450 enzyme systems.The subsequent loss of normal sterols correlates with the accumulation of 14α-methyl sterols in fungi, which may be responsible for voriconazole’s fungistatic and fungicidal activity.In vitro, voriconazole displays broad-spectrum antifungal activity with high potency against Candida species (including fluconazole-resistant strains) and fungicidal activity against Aspergillus species. It also shows activity against emerging fungal pathogens like Scedosporium and Fusarium.
Dosage in Adults
- Loading dose: 6 mg/kg IV every 12 hours for the first 24 hours
- Maintenance dose: 4 mg/kg IV every 12 hours or 200 mg orally every 12 hours
- Oral dose for patients <40 kg: 100 mg or 150 mg every 12 hours
Dosage in Pediatric Patients 2 to <12 years
- Loading dose: 9 mg/kg IV every 12 hours for the first 24 hours
- Maintenance dose: 8 mg/kg IV every 12 hours or 9 mg/kg (max 350 mg) orally every 12 hours
Administration
- Reconstitute voriconazole injection to 10 mg/mL and further dilute to ≤5 mg/mL before IV infusion over 1-3 hours
- Avoid IV administration in moderate to severe renal impairment (CrCl <50 mL/min)
Storage
- Store voriconazole powder for injection at 20-25°C (68-77°F)
- Reconstituted solution is stable for 24 hours at 2-8°C
Reviews
Voriconazole is generally well-tolerated, with the most common adverse effects being visual disturbances, fever, rash, vomiting, nausea, diarrhea, headache, and liver function test abnormalities. Careful monitoring of renal and hepatic function is recommended during treatment.
Reviews
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