Examples of using Tocilizumab 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
The adjusted mean change in the pain VAS after 12 weeks of tocilizumab treatment was a reduction of 41 points on a scale of 0- 100 compared to a reduction of 1 for placebo patients p< 0.0001.
The adjusted mean change in the pain VAS after 40 weeks of tocilizumab treatment was 32.4 mm on a 0-100 mm scale compared to a reduction of 22.3 mm for placebo patients highly statistically significant; p=0.0076.
was significantly higher in patients receiving tocilizumab(28-34%) compared to 1-12% of control patients at 24 weeks.
was higher for tocilizumab subcutaneous every other week(58%) versus placebo 46.8.
The active substance is tocilizumab.
RoActemra contains the active substance tocilizumab.
It contains the active substance tocilizumab.
The t1/ 2 of tocilizumab was concentration-dependent.
RoActemra 162 mg solution for injection in pre-filled syringe Tocilizumab.
RoActemra 20 mg/ml concentrate for solution for infusion Tocilizumab.
Tocilizumab has been shown to inhibit sIL-6R and mIL-6R-mediated signalling.
Lactation It is unknown whether tocilizumab is excreted in human breast milk.
The excretion of tocilizumab in milk has not been studied in animals.
Each 10 ml vial contains 200 mg tocilizumab 20 mg/ml.
Tocilizumab AUC, Cmin and Cmax increased with increase of body weight.
Tocilizumab binds specifically to both soluble
These results are consistent with those observed in patients treated with intravenous tocilizumab.
After week 52, all patients could receive open-label treatment with tocilizumab 8 mg/kg.
Actemra/RoActemra tocilizumab rheumatoid arthritis signs
Efficacy and safety of tocilizumab in patients with systemic juvenile idiopathic arthritis.