Fluorometholone Ophthalmic Suspension 0.02% "NITTO" (フルオロメトロン点眼液0.02%「ニットー」) Japan - engleski - すりの適正使用協議会 RAD-AR Council, Japan

fluorometholone ophthalmic suspension 0.02% "nitto" (フルオロメトロン点眼液0.02%「ニットー」)

nitto medic co., ltd. - fluorometholone - slightly viscous and white sterile ophthalmic suspention, 5ml, (cap) baby pink, (label) clear label with baby pink band, (bottle) clear

Fluorometholone Ophthalmic Suspension 0.1%"NITTO" (フルオロメトロン点眼液0.1%「ニットー」) Japan - engleski - すりの適正使用協議会 RAD-AR Council, Japan

fluorometholone ophthalmic suspension 0.1%"nitto" (フルオロメトロン点眼液0.1%「ニットー」)

nitto medic co., ltd. - fluorometholone - slightly viscous and white sterile ophthalmic suspention, 5ml, (cap) pink, (label) clear label with pink band, (bottle) clear

Allergan Fluorometholone ophthalmic Novi Zeland - engleski - Medsafe (Medicines Safety Authority)

allergan fluorometholone ophthalmic

allergan new zealand ltd - fluorometholone 1 mg/ml - eye drops, solution - 0.1% w/v - active: fluorometholone 1 mg/ml excipient: benzalkonium chloride dibasic sodium phosphate heptahydrate monobasic sodium phosphate monohydrate polysorbate 80 polyvinyl alcohol purified water sodium chloride sodium edetate sodium hydroxide

fluor-op- fluorometholone suspension Sjedinjene Američke Države - engleski - NLM (National Library of Medicine)

fluor-op- fluorometholone suspension

novartis ophthalmics - fluorometholone (unii: sv0csg527l) (fluorometholone - unii:sv0csg527l) - suspension - 0.1 ml in 100 ml - fluor-op is indicated for the treatment of corticosteroid-responsive inflammation of the palpebral and bulbar conjunctiva, cornea and anterior segment of the globe. fluor-op suspension is contraindicated in most viral diseases of the cornea and conjunctiva, including epithelial herpes simplex keratitis (dendritic keratitis), vaccinia, and varicella, and also in mycobacterial infection of the eye and fungal diseases of ocular structures. fluor-op suspension is also contraindicated in individuals with known or suspected hypersensitivity to any of the ingredients of this preparation and to other corticosteroids.

fml-s- fluorometholone and sulfacetamide sodium suspension Sjedinjene Američke Države - engleski - NLM (National Library of Medicine)

fml-s- fluorometholone and sulfacetamide sodium suspension

allergan, inc. - fluorometholone (unii: sv0csg527l) (fluorometholone - unii:sv0csg527l), sulfacetamide sodium (unii: 4nrt660kjq) (sulfacetamide - unii:4965g3j0f5) - suspension - 1.0 mg in 1 ml - fml-s® ophthalmic suspension is indicated for steroid-responsive inflammatory ocular conditions for which a corticosteroid is indicated and where superficial bacterial ocular infection or a risk of bacterial ocular infection exists. ocular steroids are indicated in inflammatory conditions of the palpebral and bulbar conjunctiva, cornea and anterior segment of the globe, where the inherent risk of steroid use in certain infective conjunctivitides is accepted to obtain a diminution in edema and inflammation. they are also indicated in chronic anterior uveitis and corneal injury from chemical, radiation or thermal burns or penetration of foreign bodies. the use of a combination drug with an anti-infective component is indicated where the risk of superficial ocular infection is high or where there is an expectation that potentially dangerous numbers of bacteria will be present in the eye. the anti-infective drug in this product, sulfacetamide, is active against the following common bacterial eye pathogens: esche

Flarex 1mg/ml, eye drops, suspension Malta - engleski - Medicines Authority

flarex 1mg/ml, eye drops, suspension

novartis ireland limited vista building, elm park, merrion road, ballsbridge, dublin 4,, ireland - fluorometholone acetate - eye drops, suspension - fluorometholone acetate 1 mg/ml - ophthalmologicals

FLAREX- fluorometholone acetate suspension/ drops Sjedinjene Američke Države - engleski - NLM (National Library of Medicine)

flarex- fluorometholone acetate suspension/ drops

eyevance pharmaceuticals - fluorometholone acetate (unii: 9i50c3i3ok) (fluorometholone - unii:sv0csg527l) - flarex (fluorometholone acetate ophthalmic suspension) 0.1% is indicated for use in the treatment of steroid responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the eye. contraindicated in acute superficial herpes simplex keratitis, vaccinia, varicella, and most other viral diseases of cornea and conjunctiva; mycobacterial infection of the eye; fungal diseases; acute purulent untreated infections, which like other diseases caused by microorganisms, may be masked or enhanced by the presence of the steroid; and in those persons who have known hypersensitivity to any component of this preparation.

FML Liquifilm 0.1% w/v Sterile Eye Drops Suspension Irska - engleski - HPRA (Health Products Regulatory Authority)

fml liquifilm 0.1% w/v sterile eye drops suspension

allergan pharmaceuticals ireland - fluorometholone - eye drops, suspension - 0.1 percent weight/volume - corticosteroids, plain; fluorometholone

FML Liquifilm 0.1% w/v Sterile Eye Drops Suspension Irska - engleski - HPRA (Health Products Regulatory Authority)

fml liquifilm 0.1% w/v sterile eye drops suspension

abbvie limited - fluorometholone - eye drops, suspension - corticosteroids, plain; fluorometholone

Flucon Novi Zeland - engleski - Medsafe (Medicines Safety Authority)

flucon

novartis new zealand ltd - fluorometholone 0.1%{relative} (+5% overage) - eye drops, suspension - 0.1% w/v - active: fluorometholone 0.1%{relative} (+5% overage) excipient: benzalkonium chloride dibasic sodium phosphate disodium edetate dihydrate hydrochloric acid hypromellose monobasic sodium phosphate monohydrate polysorbate 80 polyvinyl alcohol purified water sodium chloride sodium hydroxide