Exemple de utilizare a Initial loading în Engleză și traducerile lor în Română
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The recommended initial loading dose is 8 mg/kg body weight.
This initial loading dose is based on body weight and on the pretreatment antithrombin activity level.
As a three-weekly regimen the recommended initial loading dose of Herceptin is 8 mg/kg body weight.
After this initial loading phase, your muscle cells will be saturated with creatine and ready for the maintenance phase.
This can be achieve in a number of different methods however it appears that an initial loading protocol followed by sustained dosages is the ideal way to quickly reach and keep saturation levels.
This initial loading dose is based on body weight and on the pretreatment antithrombin activity level.
Patients assigned to receive Herceptin were given an initial loading dose of 8 mg/ kg, followed by 6 mg/ kg every three weeks for one year.
If the initial loading dose was well tolerated, the subsequent doses can be administered as a 30-minute infusion.
This can be attain in several various methods but it appears that an initial loading procedure followed by continual dosages is the ideal way to quickly reach and keep saturation levels.
Initial loading dose of 8 mg/ kg body weight, followed by 6 mg/ kg body weight 3 weeks later and then 6 mg/ kg repeated at 3-weekly intervals administered as infusions over approximately 90 minutes.
This also means that you won't need to perform an initial loading phase, as is often the case with more simplistic creatine monohydrate supplements.
Initial loading dose of 8 mg/ kg body weight, followed by 6 mg/ kg body weight 3 weeks later and then 6 mg/ kg repeated at 3-weekly intervals administered as infusions over approximately 90 minutes.
Patients assigned to receive Herceptin were given an initial loading dose of 8 mg/kg, followed by 6 mg/kg every three weeks for either one or two years.
As a weekly regimen(initial loading dose of 4 mg/kg followed by 2 mg/kg every week) concomitantly with paclitaxel following chemotherapy with doxorubicin and cyclophosphamide.
Although a great variability is observedin the premature population, peak plasma concentrations are measured around 35-40 mg/ l after the initial loading dose of 10 mg/ kg as well as after the last maintenance dose, whatever gestational and postnatal age.
The recommended initial loading dose of Herceptin is 4 mg/kg body weight.
This can be achieve in several various ways however it appears that an initial loading protocol followed by sustained doses is the ideal method to quickly reach and maintain saturation levels.
The recommended initial loading dose of RIXUBIS was to ensure that during surgery, factor IX activity levels of 80-100% for major surgeries and 30-60% for minor surgeries were maintained.
When administered with Perjeta the recommended initial loading dose of trastuzumab is 8 mg/kg body weight administered as an intravenous infusion followed every 3 weeks thereafter by a maintenance dose of 6 mg/kg body weight.
The recommended initial loading dose of Perjeta is 840 mg administered as a 60 minute intravenous infusion, followed every 3 weeks thereafter by a maintenance dose of 420 mg administered over a period of 30 to 60 minutes.
If the time between two sequential infusions is 6 weeks or more, the initial loading dose of 840 mg Perjeta should be re-administered as a 60-minute intravenous infusion followed every 3 weeks thereafter by a maintenance dose of 420 mg administered over a period of 30 to 60 minutes.
In the adjuvant setting,Herceptin has also been investigated as a weekly regimen(an initial loading dose of 4 mg/ kg followed by 2 mg/ kg every week for one year) concomitantly with paclitaxel(administered weekly(80 mg/ m2) or every 3 weeks(175 mg/ m2) for a total of 12 weeks) following 4 cycles of AC(doxorubicin 60 mg/ m2 IV push concurrently with cyclophosphamide 600 mg/ m2 over 20- 30 minutes).
In a study of 276 ACS patients managed with PCI,switching from an initial loading dose of 600 mg clopidogrel or placebo administered upon presentation to the hospital prior to coronary angiography to a 60 mg loading dose of prasugrel administered at the time of percutaneous coronary intervention, resulted in a similar increased inhibition of platelet aggregation for the 72 hour duration of the study.
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