Examples of using Crcl in English and their translations into Polish
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Ecclesiastic
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Financial
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Official/political
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Programming
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Computer
There was no adverse effect on renal function as determined by estimated glomerular filtration rate or CrCL at Week 12 and Week 52.
Renal safety with tenofovir has only been studied to a very limited degree in patients with impaired renal function CrCl< 80 ml/ min.
Patients with renal impairment(CrCl< 50 mL/min)
Limited clinical data(n=5) are available in subjects with moderate renal impairment CrCl 50 ml/min.
adverse events leading to death than patients with a CrCl≥50 mL/min see section 4.2 and 5.2.
severe renal impairment(CrCl< 50 ml/min)
CrCl< 60mL/min as it has not been studied in this population see sections 4.4 and 5.2.
For patients with moderate renal impairment(CrCl 30 to< 50 mL/min), the dose of
In patients with moderate renal impairment(40 mL/min CrCl 60 mL/min),
In patients with severe renal impairment(20 mL/min CrCl 40 mL/min)
Pharmacokinetic data in patients with severe renal impairment(CrCl 15-29 mL/min)
The study included 8 subjects with normal renal function(CrCl≥ 80 mL/min),
This method is recommended when assessing patients' CrCL prior to and during Pradaxa treatment.
There are no clinical data on the use of INCIVO in HCV patients with moderate or severe renal impairment(CrCl≤ 50 ml/min) see section 4.4.
There is insufficient data to make specific dosage adjustment recommendations for patients with severe renal impairment(CrCL≤ 30 ml/min)
Binet stages, CrCl, CIRS score,
Renal impairment In a clinical study performed in non-diabetic subjects covering a wide range of renal function(CrCl> 80 ml/ min, 30-50 ml/ min,< 30 ml/ min),
severe renal impairment(eGFR< 60 mL/min/1.73 m2 or CrCl< 60 mL/min)
In a clinical study performed in non-diabetic subjects covering a wide range of renal function(CrCl> 80 ml/min,
adverse events leading to death than patients with a CrCl≥50 mL/min see section 4.2,