Australia - English - Department of Health (Therapeutic Goods Administration)

abbvie pty ltd - phenylephrine hydrochloride, quantity: 1.2 mg/ml; prednisolone acetate, quantity: 10 mg/ml - eye drops, suspension - excipient ingredients: benzalkonium chloride; sodium metabisulfite; sodium citrate dihydrate; sodium chloride; boric acid; hypromellose; disodium edetate; phenazone; polysorbate 80; purified water; hydrochloric acid; sodium hydroxide - severe inflammation (non-infectious) of the eye, such as acute iritis, iridocyclitis, scleritis, episcleritis, uveitis, resistant ocular allergy and inflammation following surgery (where no infectious aetiology is suspected), particularly where unusually rapid control of the inflammation is required.

United States - English - NLM (National Library of Medicine)

allergan, inc. - prednisolone acetate (unii: 8b2807733d) (prednisolone - unii:9phq9y1olm) - pred forte ® is indicated for the treatment of steroid-responsive inflammation of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe. pred forte ® suspension is contraindicated in acute untreated purulent ocular infections, 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. pred forte ® suspension is also contraindicated in individuals with known or suspected hypersensitivity to any of the ingredients of this preparation and to other corticosteroids.

New Zealand - English - Medsafe (Medicines Safety Authority)

abbvie limited - prednisolone acetate 1%{relative};   - eye drops, solution - 1 % - active: prednisolone acetate 1%{relative}   excipient: benzalkonium chloride boric acid hydrochloric acid hypromellose polysorbate 80 purified water sodium chloride sodium citrate dihydrate sodium edetate sodium hydroxide - pred forte® is indicated for the treatment of steroid-responsive inflammation of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe.

Ireland - English - HPRA (Health Products Regulatory Authority)

allergan pharmaceuticals ireland - prednisolone acetate - eye drops, suspension - 1 percent weight/volume - corticosteroids, plain; prednisolone

Australia - English - Department of Health (Therapeutic Goods Administration)

bausch & lomb australia pty ltd - prednisolone sodium phosphate, quantity: 5 mg/ml - eye drops, solution - excipient ingredients: sodium hydroxide; sodium chloride; monobasic sodium phosphate; disodium edetate; purified water - non-infected inflammatory conditions of the eye.

Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

abbvie sa-nv - prednisolone acetate 1 g/100 ml - eye drops, solution - 1 % - prednisolone acetate 10 mg/ml - prednisolone

Ireland - English - HPRA (Health Products Regulatory Authority)

abbvie limited - prednisolone acetate - eye drops, suspension - corticosteroids, plain; prednisolone

Kenya - English - Pharmacy and Poisons Board

allergan pharmaceuticals (pty) ltd 30 new road (entrance off bavaria road), - prednisolone acetate - eye drops - 10 mg/ml prednisolone acetate - ophthalmological anti-infectives: sulfonamides

Saudi Arabia - English - SFDA (Saudi Food and Drug Authority)- الهيئة العامة للغذاء والدواء

amman pharmaceutical industries (api), jordan - prednisolone - eye drops - 1 %

Saudi Arabia - English - SFDA (Saudi Food and Drug Authority)- الهيئة العامة للغذاء والدواء

amman pharmaceutical industries (api), jordan - prednisolone - eye drops - 1 %