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This site contains information for healthcare professionals about LUCENTIS.
LUCENTIS 0.5 mg is indicated in adults for1:
- The treatment of neovascular (wet) age-related macular degeneration (AMD)
- The treatment of visual impairment due to diabetic macular oedema (DMO)
- The treatment of proliferative diabetic retinopathy (PDR)
- The treatment of visual impairment due to macular oedema secondary to retinal vein occlusion (branch RVO or central RVO)
- The treatment of visual impairment due to choroidal neovascularisation (CNV).
LUCENTIS 0.2 mg is indicated in preterm infants for1:
- The treatment of retinopathy of prematurity (ROP) with zone I (stage 1+, 2+, 3 or 3+), zone II (stage 3+) or AP-ROP (aggressive posterior ROP) disease.
Reference
- LUCENTIS® (ranibizumab) Summary of Product Characteristics, July 2020.