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Lucentis — Description, Dosage, Side Effects | PillsCard
OTC
Lucentis
INN: ranibizumab
Data updated: 2026-05-02
Available in:
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About This Product
Manufacturer
User Reviews
Reviews reflect personal experiences and are not medical advice. Always consult your doctor.
Novartis Europharm Limited
ATC Code
S01LA04
Source
EMA · EMEA/H/C/000715
(
ARTG
)
Lucentis (ranibizumab) is indicated in adults for:, the treatment of neovascular (wet) age-related macular degeneration (AMD),
the treatment of visual impairment due to diabetic macular oedema (DME),
treatment of proliferative diabetic retinopathy (PDR),
the treatment of visual impairment due to choroidal neovascularisation (CNV),
the treatment of visual impairment due to choroidal neovascularisation (CNV) secondary to
pathologic myopia (PM),
the treatment of visual impairment due to macular oedema secondary to retinal vein occlusion
(RVO).,Lucentis is indicated in preterm infants for:
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.
⚠️ Warnings
• Caution should be exercised in patients with history of increased eye pressure, undergone for light therapy, any allergy, who are taking other medications, during pregnancy and breastfeeding.
• It may cause vision changes, do not drive a car or operate machinery while taking this medication.
• Perform eye exams regularly while taking this medication.