Examples of using Lucentis is 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
How Lucentis is given.
The active substance in Lucentis is ranibizumab.
What Lucentis is used for.
This information will be taken into account to evaluate if Lucentis is the appropriate treatment for you.
Lucentis is given as an injection into the eye.
The recommended dose for Lucentis is 0.5 mg 0.05 ml.
Lucentis is a solution for injection in a pre-filled syringe.
The active substance in Lucentis is ranibizumab 10 mg/ ml.
Lucentis is a solution which is injected into the eye.
What Lucentis looks like and contents of the pack Lucentis is a solution for injection in a vial 0.23 ml.
Lucentis is used to treat adults with.
The Committee for Medicinal Products for Human Use(CHMP) noted that Lucentis is associated with side effects, but that this is balanced by benefits that have been shown convincingly and maintained for up to two years.
Lucentis is a solution for injection in a vial 0.23 ml.
The MAH shall ensure that, following discussions and agreements with the NationalCompetent Authorities in each Member State where Lucentis is marketed, at launch and after launch all ophthalmological clinics where Lucentis is expected to be used are provided with an up-to-date physician information pack containing the following elements.
Lucentis is marketed outside the United States by Novartis.
Treatment with Lucentis is for intravitreal injection only.
Lucentis is used to treat patients with the‘ wet' form of age-related macular degeneration AMD.
The recommended dose for Lucentis is 0.5 mg given as a single intravitreal injection.
Lucentis is not recommended during breast-feeding because it is not known whether Lucentis. .
Children and adolescents Lucentis is not recommended for use in children and adolescents due to a lack of data on safety and efficacy in these sub-populations.
Lucentis is used in adults to treat several eye diseases causing vision impairment.
Lucentis is indicated for the treatment of neovascular(wet) age-related macular degeneration(AMD) see section 5.1.
Lucentis is not recommended during breast-feeding because it is not known whether Lucentis passes into human milk.
Lucentis is the first VEGF inhibitor specifically designed for use in the eye to bind to and inhibit VEGF-A, a protein that is believed to play a critical role in the formation of new blood vessels(angiogenesis) and the hyperpermeability(leakiness) of the vessels.
Lucentis was more effective at preventing a worsening of vision than its comparators.
In diabetic macular oedema, Lucentis was more effective at improving vision than its comparators.
For diabetic macular oedema, Lucentis was studied in two main studies involving a total of 454 patients.
For choroidal neovascularisation due to pathologic myopia, Lucentis was compared with verteporfin PDT in one main study involving 277 patients.
For macular oedema due to retinal vein occlusion, Lucentis was looked at in two main studies involving a total of 789 patients, where Lucentis was compared with a sham injection.