Examples of using Eylea in English and their translations into Hungarian
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Colloquial
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Official
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Medicine
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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
Although the systemic exposure after ocular administration is very low, Eylea should not be used during pregnancy unless the potential benefit outweighs the potential risk to the foetus.
Eylea can help to stabilise,
A low incidence rate of arterial thromboembolic events was observed in the Eylea clinical trials in patients with AMD,
Eylea has not been studied in patients with active systemic infections
In COPERNICUS, 67.5%(n= 77) of the Eylea group and 68.5%(n= 50) of the sham group had perfused CRVO at baseline.
Eylea should not be used during pregnancy unless the potential benefit outweighs the potential risk to the unborn child.
These proportions were maintained at week 100 with 76.8%(n= 76) in the Eylea group and 78%(n= 39) in the sham group.
Eylea should not be used in pregnancy unless the potential benefit outweighs the potential risk to the foetus(see section 4.6).
anatomic outcomes indicate that the patient is not benefiting from continued treatment, Eylea should be discontinued.
Eylea was also investigated in two other main studies involving 366 patients with macular oedema following CRVO.
pregnant women should not use Eylea.
Eylea was investigated in two main studies involving a total of around 2,400 patients with the wet form of AMD.
In myopic choroidal neovascularisation, Eylea was investigated in a main study involving 122 patients, which compared Eylea with a sham injection.
Before Lucentis, Avastin, and Eylea, patients generally ended up legally blind with a scar[in the fundus] that was very obvious,” she said.
These compared monthly injections of Eylea 2 mg with a sham injection using a syringe without a needle.
Eylea should not be used in pregnancy unless the potential benefit outweighs the potential risk to the unborn child.
Adjunctive use of verteporfin photodynamic therapy(PDT) and Eylea has not been studied, therefore, a safety profile is not established.
You should not use Eylea if you are allergic to aflibercept,
Eylea administered 2 mg every 4 weeks(Eylea 2Q4); and macular laser photocoagulation(active control).
These proportions were maintained at week 100 with 76.8%(n= 76) in the Eylea group and 78%(n= 39) in the sham group.
