Voorbeelden van het gebruik van Times the upper limit in het Engels en hun vertalingen in het Nederlands
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Ketoconazole HRA should not be administered when liver enzymes are greater than 2 times the upper limit of normal or in association with other hepatotoxic drugs.
1% of subjects experienced elevations of ALT from normal levels to greater than 5 times the upper limit of normal(ULN), see section 4.8.
Therapy with AVANDAMET should not be initiated in patients with increased baseline liver enzyme levels(ALT> 2.5 times the upper limit of normal) or with any other evidence of liver disease.
Renal impairment: no clinical trials were conducted with SPRYCEL in patients with decreased renal function trials excluded patients with serum creatinine concentration> 1.5 times the upper limit of the normal range.
persistent elevations of serum transaminases to greater than 5 times the upper limit of the normal range,
Laboratory test findings Transient emergent increases(> 3 times the upper limit of the normal range)
if related to disease) times the upper limit of the normal range and/ or total bilirubin> 1.5 times the upper limit of the normal range.
For patients with baseline alanine transaminase up to 3.7 times the upper limit of normal baseline albumin ranging from 15 to 58 g/L,
Aclasta was studied in male and female patients aged above 30 years with primarily mild to moderate Paget's disease of the bone(median serum alkaline phosphatase level 2.6-3.0 times the upper limit of the age-specific normal reference range at the time of study entry)
develop severe hepatic impairment(bilirubin> 3 times the upper limit of normal[ULN]; transaminases>
Zoledronic acid was studied in male and female patients aged above 30 years with primarily mild to moderate Paget's disease of the bone(median serum alkaline phosphatase level 2.6-3.0 times the upper limit of the age-specific normal reference range at the time of study entry) confirmed by radiographic evidence.
Hepatic impairment: no clinical trials were conducted with SPRYCEL in patients with moderate to severe hepatic impairment trials excluded patients with ALT and/ or AST> 2.5 times the upper limit of the normal range and/ or total bilirubin> 2 times the upper limit of the normal range.
3 times the upper limit of the normal range.
ALAT greater than 5 times the Upper Limit Normal(ULN) until baseline ASAT/ ALAT is stabilised at less than 5X ULN,
AST/SGOT up to 3 times the upper limit of the normal range(ULN)), bilirubin and/or gamma-glutamyl transferase(GGT) levels.
greater than 1.5 times the upper limit of the normal range(ULN)
alkaline phosphatase tests did not exceed 5 times the upper limit of normal.
greater than 1.5 times the upper limit of the normal range(ULN) and alkaline phosphatase greater
female patients aged above 30 years with primarily mild to moderate Paget' s disease of the bone(median serum alkaline phosphatase level 2.6- 3.0 times the upper limit of the age-specific normal reference range at the time of study entry) confirmed by radiographic evidence.
RCC Clinical Trial 1 was a Phase 3, multi-centre, 3-arm, randomised, open-label study in previously untreated patients with advanced renal cell carcinoma and with 3 or more of 6 pre-selected prognostic risk factors less than 1 year from time of initial renal cell carcinoma diagnosis to randomisation, Karnofsky performance status of 60 or 70, haemoglobin less than the lower limit of normal, corrected calcium of greater than 10 mg/ dl, lactate dehydrogenase 1.5 times the upper limit of normal, more than 1 metastatic organ site.