Примери за използване на Ribavirin dose на Английски и техните преводи на Български
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in subjects randomized to receive ribavirin dose reduction and 2%(5/251) in subjects randomized to receive erythropoietin.
The potential negative impact of ribavirin dose reduction on efficacy results could not be ruled out.
a patient has a serious adverse reaction potentially related to ribavirin, the ribavirin dose should be modified
If a patient has a serious adverse reaction potentially related to ribavirin, the ribavirin dose should be modified
Superior efficacy has been demonstrated with the combination of pegylated interferon with ribavirin(sustained response rate of 61% achieved in a study performed in naïve patients with a ribavirin dose> 10.6 mg/kg, p< 0.01).
of subjects had ribavirin dose reductions due to adverse reactions.
was comparable to subjects who maintained their starting ribavirin dose throughout treatment.
In the 8.5% of subjects who had ribavirin dose adjustments during therapy, the SVR rate(98.5%)
In a study comparing the use of ribavirin dose reduction and erythropoesis stimulating agents in the management of treatment-emergent anaemia,
severe renal impairment, ribavirin dose adjustments are recommended in adult patients with creatinine clearance< 50 mL/minute.
with additional anaemia interventions, including the use of erythropoietin or ribavirin dose reduction.
If a patient has a serious adverse reaction potentially related to ribavirin, the ribavirin dose should be modified
For subjects who received ribavirin, the ribavirin dose was 1000 mg per day for subjects weighing less than 75 kg
for subjects randomized to receive ribavirin dose reduction; 68.5%(172/251) for subjects randomized to receive.
were randomized to using either ribavirin dose reduction or erythropoietin(N=500).
all patients received Pegasys 180 μ g sc qw and a ribavirin dose of 800 mg and were randomized to
all patients received Pegasys 180 mcg sc qw and a ribavirin dose of 800 mg and were randomised to
The ribavirin dose was weight-based(1,000 mg daily administered in two divided doses for patients< 75 kg
during the overall treatment phase the ribavirin dose was further reduced in 36.5% of patients,
If patients maintained haemoglobin levels≥12 g/dL, ribavirin dose was increased at weeks 2, 4, and up to every 4 weeks until the appropriate weight-based dose