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Pharmacy title
LUCENTIS® (ranibizumab injection) for Wet AMD and Macular Edema following RVO
Information and data for healthcare professionals about LUCENTIS® (ranibizumab injection) for the treatment of wet age-related macular degeneration and rapid and sustained visual improvement in retinal vein occlusion. INDICATION: LUCENTIS® (ranibizumab injection) is indicated for the treatment of patients with: Neovascular (Wet) Age-Related Macular Degeneration (AMD) and Macular Edema Following Retinal Vein Occlusion (RVO). IMPORTANT SAFETY INFORMATION LUCENTIS is contraindicated in patients with ocular or periocular infections or hypersensitivity to ranibizumab or any of the excipients in LUCENTIS. Intravitreal injections, including those with LUCENTIS, have been associated with endophthalmitis, retinal detachment, and iatrogenic traumatic cataract. Increases in intraocular pressure have been noted within 60 minutes of intravitreal injection. Although there was a low rate of arterial thromboembolic events (ATEs) observed in the LUCENTIS clinical trials, there is a potential risk of ATEs following intravitreal use of VEGF inhibitors. ATEs are defined as nonfatal stroke, nonfatal myocardial infarction, or vascular death (including deaths of unknown cause). In the LUCENTIS Phase III clinical trials, most common ocular side effects included conjunctival hemorrhage, eye pain, vitreous floaters, vitreous detachment, maculopathy, and intraocular inflammation. Most common non-ocular side effects included headache, arthralgia, influenza, nasopharyngitis, sinusitis, and bronchitis. For additional safety information, please see LUCENTIS full prescribing information.
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Country
United States, USA (US)
City
South San Francisco
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