Examples of using Soliris in English and their translations into Norwegian
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Colloquial
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Ecclesiastic
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Ecclesiastic
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Computer
If aHUS patients discontinue treatment with Soliris, they should be monitored closely for signs
In aHUS patients, uncontrolled terminal complement activation and the resulting complement- mediated thrombotic microangiopathy are blocked with Soliris treatment.
In PNH patients, uncontrolled terminal complement activation and the resulting complement- mediated intravascular haemolysis are blocked with Soliris treatment.
Prior to initiating Soliris therapy, it is recommended that PNH
Soliris administration should be interrupted in all patients experiencing severe infusion reactions and appropriate medical therapy administered.
Soliris treatment may reduce your natural resistance to infections,
Soliris vials in the original package may be removed from refrigerated storage for only one single period of up to 3 days.
up to 127 weeks following discontinuation of Soliris treatment in some patients.
with median duration of Soliris therapy of 50 weeks range: 13 weeks to 86 weeks.
Twenty of the 24 patients who required dialysis at baseline were able to discontinue dialysis during Soliris treatment.
Four of the five patients who required dialysis at study entry were able to discontinue dialysis for the duration of Soliris treatment, and one patient developed a new dialysis requirement.
discontinued Soliris treatment with a median follow-up period of 24 weeks.
In paediatric PNH and aHUS patients with body weight below 40 kg, the Soliris dosing regimen consists of.
When Soliris treatment was continued for more than 26 weeks,
When Soliris treatment was continued for more than 26 weeks,
If serious haemolysis occurs after Soliris discontinuation, consider the following procedures/treatments: blood transfusion(packed RBCs), or exchange transfusion if the PNH RBCs are>
The median duration of Soliris therapy was 16 weeks(range 4 to 70 weeks)
To reduce the risk of infection, all patients must be vaccinated at least 2 weeks prior to receiving Soliris unless the risk of delaying Soliris therapy outweigh the risks of developing a meningococcal infection.
Additionally, all patients must be vaccinated against meningococcus at least 2 weeks prior to receiving Soliris unless the risk of delaying Soliris therapy outweigh the risks of developing a meningococcal infection.
in untreated patients and the clinical outcomes during Soliris treatment.