Examples of using Dosing regimen in English and their translations into Polish
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Table 10 Geometric mean(95% CI) steady-state plasma eltrombopag pharmacokinetic parameters in paediatric subjects with ITP 50 mg once daily dosing regimen.
These results suggest that the QTc liability is reduced with the modified Invirase/ritonavir dosing regimen, based on a cross-study comparison in a different population Table 4.
When this dosing regimen is impractical due to the recommended administration of OSSEOR at bedtime,
At the recommended dosing regimen, serum concentration generally reached steady-state by Week 8 in the initial phase following transplantation
Summary of the Phase 3 Clinical Trials Program- 75 mg and/or 150 mg every 2 weeks(Q2W) dosing regimen.
The dosing regimen used for this study is unlikely to be sustained in the clinical setting.
follow GL3 clearance in kidney and skin tissues at an alternative dosing regimen.
This dosing regimen for paediatric patients weighing 14-30 kg is based primarily on pharmacokinetic modelling, with supporting data from clinical studies.
net Protocol T) utilised a dosing regimen based on strict OCT
using the three-weekly(q3w) dosing regimen, was investigated in study MO22982 see section 4.8.
The pharmacokinetic guided dosing regimen(according to a specific formula) was targeted to maintain factor VIII
aHUS patients with body weight below 40 kg, the Soliris dosing regimen consists of.
Children weighing 75 kg or more should be administered ORENCIA following the adult dosing regimen.
The dosing regimen of the lamivudine component of DUTREBIS in the paediatric population is the same as the dosing regimen of the individual component EPIVIR.
In subjects with multiple sclerosis, two 240 mg doses were administered 4 hours apart as part of a three times a day dosing regimen.
The clinical relevance of these observed effects for animals vaccinated while being administered oclacitinib(in accordance with the recommended dosing regimen) is unclear.
an alternating daily dosing regimen of 800 mg and 400 mg in patients with severe renal impairment can approximate the AUC(0-48h)
The dosing regimen in paediatric patients and adolescents weighing less than 40 kg was defined based on a pharmacokinetic(PK)
The safety profile in patients treated with a 300 mg once every 4 week(monthly) dosing regimen, was similar to the safety profile as described for the clinical studies program using a 2 week dosing regimen, except for a higher rate of local injection site reactions.
Patients should be maintained on a single formulation of tacrolimus with the corresponding daily dosing regimen; alterations in formulation or regimen should only