ACULAR 0.5 %w/v Eye Drops Solution Ireland - English - HPRA (Health Products Regulatory Authority)

acular 0.5 %w/v eye drops solution

g & a licensing limited - ketorolac trometamol - eye drops solution - 0.5 %w/v

ACULAR 0.5 %w/v Eye Drops Solution Ireland - English - HPRA (Health Products Regulatory Authority)

acular 0.5 %w/v eye drops solution

ltt pharma limited - ketorolac trometamol - eye drops solution - 0.5 %w/v

Macular Saffron Complex Australia - English - Department of Health (Therapeutic Goods Administration)

macular saffron complex

nature's goodness australia pty ltd - ascorbic acid,copper gluconate,crocus sativus,d-alpha-tocopheryl acid succinate,zinc oxide -

Elektron Eye Technology Macular Pigment Screener Singapore - English - HSA (Health Sciences Authority)

elektron eye technology macular pigment screener

ning kwong optical company (private) limited - ophthalmology - macular pigment scanner (mpsii) is a computerized instrument for measuring a subject's macular pigment optical density. its purpose is to identify patients at risk of developing early stage age-related macular degeneration (amd).

EYLEA aflibercept (rch) 40 mg/mL solution for intravitreal injection pre-filled syringe Australia - English - Department of Health (Therapeutic Goods Administration)

eylea aflibercept (rch) 40 mg/ml solution for intravitreal injection pre-filled syringe

bayer australia ltd - aflibercept, quantity: 40 mg/ml - injection, solution - excipient ingredients: monobasic sodium phosphate monohydrate; sodium chloride; dibasic sodium phosphate heptahydrate; sucrose; water for injections; polysorbate 20 - eylea (aflibercept) is indicated in adults for the treatment of: - neovascular (wet) age-related macular degeneration (wet amd) - visual impairment due to macular oedema secondary to central retinal vein occlusion (crvo) - diabetic macular oedema (dme) - visual impairment due to macular oedema secondary to branch retinal vein occlusion (brvo) - visual impairment due to myopic choroidal neovascularisation (myopic cnv)

EYLEA aflibercept (rch) 40 mg/mL solution for intravitreal injection vial with needle Australia - English - Department of Health (Therapeutic Goods Administration)

eylea aflibercept (rch) 40 mg/ml solution for intravitreal injection vial with needle

bayer australia ltd - aflibercept, quantity: 40 mg/ml - injection, solution - excipient ingredients: monobasic sodium phosphate monohydrate; sucrose; polysorbate 20; sodium chloride; water for injections; dibasic sodium phosphate heptahydrate - eylea (aflibercept) is indicated in adults for the treatment of: - neovascular (wet) age-related macular degeneration (wet amd); - visual impairment due to macular oedema secondary to central retinal vein occlusion (crvo); - diabetic macular oedema (dme); - visual impairment due to macular oedema secondary to branch retinal vein occlusion (brvo); - visual impairment due to myopic choroidal neovascularisation (myopic cnv)

OZURDEX Israel - English - Ministry of Health

ozurdex

abbvie biopharmaceuticals ltd, israel - dexamethasone - implant in applicator - dexamethasone 0.7 mg - dexamethasone - dexamethasone - ozurdex is indicated for the treatment of adult patients with:• diabetic macular oedema (dme)• macular oedema following either branch retinal vein occlusion (brvo) or central retinal vein occlusion (crvo).• inflammation of the posterior segment of the eye presenting as non-infectious uveitis.

Jetrea New Zealand - English - Medsafe (Medicines Safety Authority)

jetrea

pharmaco (nz) ltd - ocriplasmin 2.5 mg/ml - concentrate for injection - 2.5 mg/ml - active: ocriplasmin 2.5 mg/ml excipient: citric acid monohydrate mannitol sodium hydroxide water for injection - jetrea is indicated in adults for the treatment of vitreomacular traction (vmt), including when associated with macular hole of diameter less than or equal to 400 microns.

LUCENTIS ranibizumab (rbe) 1.65 mg/0.165 mL solution for injection prefilled syringe Australia - English - Department of Health (Therapeutic Goods Administration)

lucentis ranibizumab (rbe) 1.65 mg/0.165 ml solution for injection prefilled syringe

novartis pharmaceuticals australia pty ltd - ranibizumab, quantity: 1.65 mg - injection, solution - excipient ingredients: histidine; histidine hydrochloride monohydrate; trehalose dihydrate; polysorbate 20; water for injections - 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),- the treatment of proliferative diabetic retinopathy (pdr),- the treatment of visual impairment due to choroidal neovascularisation.,- 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)