Examples of using Soliris in English and their translations into Hungarian
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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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Programming
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Official/political
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Computer
All patients treated with Soliris when administered as recommended demonstrated rapid
All physicians who intend to prescribe Soliris must ensure they are familiar with the physician's guide to prescribing.
Because of an increased risk of meningitis, Soliris should not be given to people who are infected with Neisseria meningitidis, or who have not been vaccinated against this bacterium.
At 6 months, patients treated with Soliris with no history of RBC transfusion had significantly(p<
Dilute Soliris to a final concentration of 5 mg/ml(initial concentration divided by 2)
Soliris has not been studied in children or in patients who have problems with their kidneys or liver.
Soliris therefore restores terminal complement regulation in the blood of PNH patients
Because of the importance of rapidly identifying and treating certain types of infection in patients who receive Soliris, you will be provided a card to carry with you,
Soliris has been studied in one main study involving 88 adult patients with PNH who had had at least four blood transfusions for anaemia in the previous year.
In addition, the company that markets Soliris will ensure that distribution of the medicine occurs only after checking that the patient has been vaccinated appropriately.
of PNH in untreated patients and the clinical outcomes during Soliris treatment.
At least two weeks before starting Soliris treatment, patients must be vaccinated against meningitis caused by the bacterium Neisseria meningitidis
Therefore, Soliris should be given to a pregnant woman only if clearly needed.
In the PNH Registry, patients treated with Soliris were observed to have a reduction in haemolysis
After completion of the initial 26-week treatment period, most patients continued to receive Soliris by enrolling into an extension study.
the disease is considered‘ rare', and Soliris was designated an‘ orphan medicine'(a medicine used in rare diseases) on 17 October 2003.
In the main study, 21(49%) of the 43 patients receiving Soliris had stable haemoglobin levels,
aHUS patients with body weight below 40 kg, the Soliris dosing regimen consists of.
The European Commission granted a marketing authorisation valid throughout the European Union for Soliris to Alexion Europe SAS on 20 June 2007.
Prior to initiating Soliris therapy, it is recommended that PNH patients should receive immunizations according to current immunization guidelines.