Active Ingredient: Voriconazole
Treatment of candidaemia in non-neutropenic patients.
For this indication, competent medicine agencies globally authorize below treatments:
Intravenous
16 - 18 mg per kg of body weight
From 8 To 9 mg per kg of body weight 2 time(s) per day every day
18 mg per kg of body weight
16 mg per kg of body weight
Voriconazole should be dosed as children as these young adolescents may metabolize voriconazole more similarly to children than to adults.
The recommended dosing regimen is as follows:
| Intravenous | Oral | |
|---|---|---|
| Loading Dose Regimen (first 24 hours) | 9 mg/kg every 12 hours | Not recommended |
| Maintenance Dose (after first 24 hours) | 8 mg/kg twice daily | 9 mg/kg twice daily (a maximum dose of 350 mg twice daily |
Note: Based on a population pharmacokinetic analysis in 112 immunocompromised paediatric patients aged 2 to <12 years and 26 immunocompromised adolescents aged 12 to <17 years.
It is recommended to initiate the therapy with intravenous regimen, and oral regimen should be considered only after there is a significant clinical improvement. It should be noted that an 8 mg/kg intravenous dose will provide voriconazole exposure approximately 2-fold higher than a 9 mg/kg oral dose.
If patient response to treatment is inadequate, the intravenous dose may be increased by 1 mg/kg steps. If patient is unable to tolerate treatment, reduce the intravenous dose by 1 mg/kg steps.
It is recommended that voriconazole is administered at a maximum rate of 3 mg/kg per hour over 1 to 3 hours.
Oral
18 - 18 mg per kg of body weight
From 9 To 9 mg per kg of body weight 2 time(s) per day every day
Voriconazole should be dosed as children as these young adolescents may metabolize voriconazole more similarly to children than to adults.
The recommended dosing regimen is as follows:
| Intravenous | Oral | |
|---|---|---|
| Loading Dose Regimen (first 24 hours) | 9 mg/kg every 12 hours | Not recommended |
| Maintenance Dose (after first 24 hours) | 8 mg/kg twice daily | 9 mg/kg twice daily (a maximum dose of 350 mg twice daily |
Note: Based on a population pharmacokinetic analysis in 112 immunocompromised paediatric patients aged 2 to <12 years and 26 immunocompromised adolescents aged 12 to <17 years.
It is recommended to initiate the therapy with intravenous regimen, and oral regimen should be considered only after there is a significant clinical improvement. It should be noted that an 8 mg/kg intravenous dose will provide voriconazole exposure approximately 2-fold higher than a 9 mg/kg oral dose.
If patient response to treatment is inadequate, the intravenous dose may be increased by 1 mg/kg steps. If patient is unable to tolerate treatment, reduce the intravenous dose by 1 mg/kg steps.
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