Examples of using Soliris in English and their translations into Croatian
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Ecclesiastic
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Soliris was studied in one main study involving 87 adults with PNH who had had at least four blood transfusions for anaemia in the previous year.
All aHUS patients treated with Soliris when administered as recommended demonstrated rapid
At least two weeks before starting Soliris treatment, patients must be vaccinated against meningitis caused by the bacterium Neisseria meningitidis
Due to its mechanism of action, Soliris therapy should be administered with caution to patients with active systemic infections.
the use of Soliris increases the patient's susceptibility to meningococcal infection Neisseria meningitidis.
If aHUS patients discontinue treatment with Soliris, they should be monitored closely for signs
If an adverse event occurs during the administration of Soliris, the infusion may be slowed or stopped at the discretion of the physician.
In aHUS patients, uncontrolled terminal complement activation and the resulting complement- mediated thrombotic microangiopathy are blocked with Soliris treatment.
In aHUS, chronic administration of Soliris resulted in a rapid
In PNH patients, uncontrolled terminal complement activation and the resulting complement- mediated intravascular haemolysis are blocked with Soliris treatment.
In PNH, chronic administration of Soliris resulted in a rapid
Quality defect report to Soliris 300 mg concentrate for solution for infusion- News- Inspection|.
Quality defect report to Soliris 300 mg concentrate for solution for infusion- News|
Prior to administration, the Soliris solution should be visually inspected for particulate matter and discolouration.
Prior to initiating Soliris therapy, it is recommended that PNH and aHUS patients should
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.
Supplemental dosing is recommended when Soliris is administered to aHUS patients receiving plasma infusion or exchange see section 4.2.
The effectiveness of Soliris treatment was assessed using a range of measurements,