Concise Prescribing Info
Neovascular (wet) age-related macular degeneration (AMD).
Dosage/Direction for Use
6 mg intravitreal inj every 4 wk for 1st 3 doses, then individualize treatment intervals based on disease activity. Patient w/o disease activity Treatment every 12 wk, patient w/ disease activity Treatment every 8 wk.
Hypersensitivity. Active or suspected ocular/periocular infections; active intraocular inflammation.
Special Precautions
Discontinue use in patients w/ rhegmatogenous retinal detachment, or stage 3 or 4 macular holes. Not to inj while IOP is ≥30 mmHg. W/hold & not to be resumed earlier than the next scheduled treatment in case of decrease in best-corrected visual acuity of ≥30 letters compared w/ last visual acuity assessment; retinal break; subretinal haemorrhage involving centre of fovea or if size of haemorrhage is ≥50% of total lesion area; performed or planned intraocular surgery w/in previous or next 28 days. Endophthalmitis, intraocular inflammation, traumatic cataract, retinal detachment; retinal vasculitis &/or vascular occlusion. Patients w/ risk factors for retinal pigment epithelial tears; history of stroke, transient ischaemic attacks or MI w/in last 3 mth; poorly controlled glaucoma. Immunogenicity. Bilateral treatment. Monitor & manage for increased IOP & optic nerve head perfusion. Not to be used concurrently w/ other systemic or ocular anti-VEGF medicinal products. May affect ability to drive or use machines. Hepatic impairment. Women of childbearing potential should use effective contraception during treatment & for at least 1 mth after last dose. Not to be used during pregnancy. Not recommended during lactation & for at least 1 mth after last dose. Childn & adolescents <18 yr.
Adverse Reactions
Hypersensitivity; reduced visual acuity, retinal haemorrhage, tear & pigment epithelial tear, uveitis, iritis, vitreous detachment & floaters, cataract, conjunctival haemorrhage, eye pain, increased IOP, conjunctivitis, blurred vision, corneal abrasion, punctate keratitis.
MIMS Class
Other Eye Preparations
ATC Classification
S01LA06 - brolucizumab ; Belongs to the class antineovasculatisation agents. Used in the management of neovascular macular degeneration.
Pagenax intraocular inj 120 mg/mL
Register or sign in to continue
Asia's one-stop resource for medical news, clinical reference and education
Already a member? Sign in