Examples of using Were comparable in English and their translations into Finnish
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Medicine
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Colloquial
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with normal renal function, ombitasvir exposures were comparable in subjects with mild, moderate and severe renal impairment.
Baseline demographics and HBV disease characteristics were comparable between the 2 treatment arms and across age cohorts.
Population pharmacokinetics estimates of exposure of elbasvir and grazoprevir were comparable between Whites and Black/African Americans.
The seroconversion rates were comparable in both groups(82 vs 83%)
qHPV vaccine were comparable and consistent with the general population.
baseline characteristics were comparable between the group receiving ISENTRESS 400 mg twice daily and the group receiving efavirenz 600 mg at bedtime.
Pharmacokinetic parameters for the respective substances were comparable after the administration of budesonide
Gimeracil and uracil AUC0-12 values were comparable between the two groups, suggesting that DPD inhibition was similar for the Asian
all uterine parameters were comparable to the controls.
Ritonavir concentrations obtained after 350 to 400 mg/m² twice daily in paediatric patients were comparable to those obtained in adults receiving 600 mg(approximately 330 mg/m²) twice daily.
Subjects with severe thrombocytopaenia or any other coagulation disorder were excluded. The VZV specific immune responses to ZOSTAVAX at Week 4 post-vaccination were comparable whether administered by SC or IM route.
Changes in anti-Factor Xa activity and INR were comparable between subjects with mild to moderate hepatic impairment and healthy subjects.
Baseline levels of the shed HER2-ECD observed in MGC patients were comparable to those in MBC and EBC patients
Mean baseline peak volume of oxygen consumed(VO2) values were comparable across the sildenafil treatment groups(17.37 to 18.03 ml/kg/min), and slightly higher for the placebo treatment group 20.02 ml/kg/min.
Antibody responses to booster doses following two-dose or three-dose infant primary series were comparable for all 13 vaccine serotypes.
Antibody responses to booster doses in toddlers following two-dose or three-dose infant series were comparable for all 7 vaccine serotypes
duration of follow-up(median=40 months) were comparable in both treatment arms.
Frequency and duration of vaccine virus shedding in these immunocompromised children and adolescents were comparable to that seen in healthy children and adolescents.
DM1 was aneugenic or clastogenic in an in vivo single-dose rat bone marrow micronucleus assay at exposures that were comparable to mean maximum concentrations of DM1 measured in humans administered trastuzumab emtansine.
The responses to all three TIV antigens were comparable when TIV was given alone or concomitantly with Prevenar 13.