Examples of using Crcl in English and their translations into German
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Financial
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Ecclesiastic
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Political
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Computer
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Programming
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Official/political
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Political
Assessment of renal function: CrCL should be monitored at the beginning of the treatment in all patients and afterwards when clinically
Moderate and severe renal impairment(patients with eGFR< 60 mL/min/1.73 m2 or CrCl< 60 mL/min),(see sections 4.2 and 4.4);
Empagliflozin should be discontinued when eGFR is persistently below 45 ml/min/1.73 m2 or CrCl persistently below 45 ml/min see sections 4.4, 4.8, 5.1, and 5.2.
No dose adjustment is required for patients with an eGFR≥60 ml/min/1.73 m2 or CrCl≥60 ml/min.
adverse events leading to death than patients with a CrCl≥50 mL/min see section 4.2 and 5.2.
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.
Table 2 shows the recommended dose adjustments for patients with estimated CrCL≤ 50 mL/min see sections 4.4 and 5.2.
Dosage adjustments are required in adults, adolescents and children with CrCL≤ 50 ml/min see section 4.2.
end-stage renal disease(creatinine clearance[CrCl]< 30 mL/min
In a small number of volunteers with severe renal insufficiency(CrCL 10- 30 ml/ min),
population pharmacokinetic analysis showed that the pharmacokinetics of darunavir were not significantly affected in HIV infected patients with moderate renal impairment(CrCl between 30-60 ml/min,
Renal impairment There is insufficient data to make specific dosage adjustment recommendations for patients with severe renal impairment(CrCL≤ 30 ml/min)
There is insufficient data to make specific dosage adjustment recommendations for patients with severe renal impairment(CrCL≤ 30 ml/min) and end-stage renal disease(ESRD),
Therefore, this medicinal product must not be used in patients with moderate to severe renal impairment patients with CrCl< 60 ml/min
Among a subgroup with baseline CrCL 30 to 50 mL/min death occurred in 16.7%(9/54)
CrCL should be closely monitored
A single-dose, open-label study evaluated the pharmacokinetics of canagliflozin 200 mg in subjects with varying degrees of renal impairment(classified using CrCl based on the Cockroft-Gault equation) compared to healthy subjects.
In subjects with end-stage renal disease(ESRD)(CrCl< 10 ml/min)
Patients with moderate renal impairment(CrCl 30 to 59 mL/min) had a higher incidence(defined as a difference of at least 5%) of≥ Grade 3 adverse events(AEs), serious AEs, and dose delays and reductions compared to the patients with normal(CrCl≥ 90 mL/min) or mild renal impairment CrCl.
Severe renal impairment(CrCl< 30ml/min)