Examples of using Trough levels in English and their translations into German
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Medicine
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IgG trough levels of at least 4-6 g/l.
Between weeks 9 and 49, median trough levels varied by less than 9.
Trough levels at 24 hours are, however, similar.
To reduce the rate of infection,it may be necessary to increase the dose and aim for higher trough levels.
The trough levels should be maintained above 5 g/l.
Plasma concentrations of dinutuximab, especially trough levels, tended to be lower in patients with HACA.
Trough levels at 24 hours are, however, similar for both formulations.
In hepatically impaired patients,it is recommended that sirolimus whole blood trough levels be closely monitored.
Increase in trough levels 75% increase in daily secretion.
Trough levels should be measured in order to adjust the dose and dosage interval.
Prograf capsules or from Advagraf prolonged-release capsules to Envarsus, trough levels should be measured prior to conversion and within two weeks after conversion.
Trough levels should be measured and assessed in conjunction with the incidence of infection.
In a clinical trial with Hizentra(n 46),the subjects achieved sustained trough levels(median 8.1 g/l) over a period of 29 weeks when receiving median weekly doses of 0.06 to 0.24 g/kg body weight.
Blood trough levels of tacrolimus should be monitored during the post-transplantation period.
In PNH patients,pharmacodynamic activity correlates directly with eculizumab serum concentrations and maintenance of trough levels above 35 microgram/ml results in essentially complete blockade of haemolytic activity in the majority of PNH patients.
Trough levels should be measured and assessed in conjunction with the incidence of infection.
It is recommended that sirolimus whole blood trough levels be closely monitored in patients with impaired hepatic function see Therapeutic drug monitoring.
Trough levels should be measured and assessed in conjunction with the patient's clinical response.
Following conversion, tacrolimus trough levels should be monitored and if necessary dose adjustments made to maintain similar systemic exposure.
Trough levels should be measured and assessed in conjunction with the patient's clinical response.
It is recommended that sirolimus whole blood trough levels be closely monitored in patients with impaired hepatic function see Therapeutic monitoring of the medicinal product and dose adjustment.
Trough levels of 5-10% have been targeted in clinical trials for achieving bleeding control while on prophylaxis.
In clinical practice, whole blood trough levels have generally been in the range of 5-20 ng/mL in kidney transplant patients in the early post- transplant period, and 5-15 ng/mL during subsequent maintenance therapy.
In clinical practice, whole blood trough levels have generally been in the range 5- 20 ng/ ml in liver transplant recipients and 10- 20 ng/ ml in kidney and heart transplant patients in the early post- transplant period.
Mean sirolimus whole blood trough levels from the same phase III trial were 7.2 ng/ ml(4.0 to 11 ng/ ml, expressed as chromatographic assay values; n=226) for the 2 mg per day dose and 14 ng/ ml(8.0 to 22 ng/ ml, expressed as chromatographic assay values; n=219) for the 5 mg per day dose see section 4.2.
Cmin( mg/ dl)/( mg/ kg) trough level.
The lowest IgG levels seen during treatment with Hizentra(average trough level of 8.1 g per litre) were comparable to those seen during previous immunoglobulin treatment.
The dose required to achieve a trough level of 6 g/l is of the order of 0.4-0.8 g/kg body weight per month.