Примери за използване на Ribavirin dose на Английски и техните преводи на Български
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Reduce ribavirin dose* if.
In Phase 3 clinical trials, 91.5% of subjects did not require ribavirin dose adjustments during therapy.
The ribavirin dose should be administered with food.
Total daily ribavirin dose(mg).
Lower ribavirin dose at initiation may be appropriate.
Subjects randomized to receive ribavirin dose reduction(N=249).
Impact of ribavirin dose adjustment on probability of SVR.
Sustained response rates with PegIntron+ ribavirin(by ribavirin dose, genotype and viral load).
Ribavirin dose reductions were used for management of anaemia.
There were 77 subjects who received≥ 5 steps ribavirin dose reduction for the management of anaemia.
Table 3: Ribavirin dose modification guideline for co-administration with Harvoni.
Table 7 Sustained response rates with ribavirin+ peginterferon alfa-2b(by ribavirin dose[mg/kg], genotype and viral load).
Ribavirin dose modification guideline for co-administration with Sovaldi in adults.
The potential negative impact of ribavirin dose reduction on efficacy results could not be ruled out.
Ribavirin dose modification guideline for co-administration with Harvoni in adults Laboratory values.
Sustained response rates with Ribavirin+ peginterferon alfa-2b(by Ribavirin dose[mg/ kg], genotype and viral load).
Use of ribavirin dose reduction versus erythropoietin in the management of anaemia in previously.
Table 9 Sustained response rates with ViraferonPeg+ ribavirin(by ribavirin dose, genotype and viral load).
Ribavirin dose reduction is the preferred strategy for managing treatment-emergent anaemia.
Table 7 Sustained response rates with ribavirin+ peginterferon alfa-2b(by ribavirin dose[mg/kg], genotype and viral load).
Ribavirin dose adjustments were performed according to the ribavirin prescribing information.
In children and adolescent patients treated with Ribavirin BioPartners plus interferon alfa-2b,reduce ribavirin dose to 7.5 mg/kg/day.
For ribavirin dose modifications, refer to the Summary of Product Characteristics of the medicinal product containing ribavirin. .
The transfusion rate was 4%(10/249)in subjects randomized to receive ribavirin dose reduction and 2%(5/251) in subjects randomized to receive erythropoietin.
Rates for using ribavirin dose reduction versus erythropoietin in the management of anaemia in previously untreated subjects.
The treatment discontinuation rate due to anaemia was 2%(5/249)in subjects randomized to receive ribavirin dose reduction and 2%(6/251) in subjects randomized to receive erythropoietin.
Ribavirin dose reduction is the preferred strategy for managing treatment-emergent anaemia(see section 5.1).
If a patient has a serious adverse reaction potentially related to ribavirin, the ribavirin dose should be modified or discontinued, if appropriate, until the adverse reaction abates or decreases in severity.
Impact of Ribavirin Dose Adjustmenton Probability of SVR In Phase 3 clinical trials, 91.5% of subjects did not require ribavirin dose adjustments during therapy.
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).