Glaucoma News

FDA Approves Bimatoprost 0.01% Eye Drops For Elevated Intraocular Pressure

Friday, September 3rd, 2010

approved bimatoprost 0.01% ophthalmic solution for the first-line treatment of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension. Medscape Medical News

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Association between primary open-angle glaucoma (POAG) and WDR36 sequence variance in Italian families affected by POAG

Thursday, September 2nd, 2010

Background/aims To assess the involvement of WDR36 sequence variance in primary open-angle glaucoma (POAG) in Italian patients. Methods A cohort of 34 Italian families affected by POAG was analysed by denaturing high-performance liquid

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Cochrane Eyes and Vision Group

Thursday, September 2nd, 2010

Neuroprotection for treatment of glaucoma in adults Glaucoma is a heterogeneous group of conditions involving progressive damage to the optic nerve, deterioration of retinal ganglion cells and ultimately visual-field loss. It is a leading cause

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Open-angle glaucoma and ocular perfusion

Thursday, September 2nd, 2010

Unit, Department of Ophthalmology, Hacettepe University, School of Medicine, Ankara, Turkey Correspondence to Dr A G P Konstas, Glaucoma Unit, 1st University Department of Ophthalmology, AHEPA Hospital, 1 Kyriakidi Str, Thessaloniki 546 36, Greece;

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Surgical Revision of Dysfunctional Filtration Blebs With Bleb Preservation, Sliding Conjunctival Flap and Fibrin Glue

Wednesday, September 1st, 2010

This article explores some of the options available in glaucoma filtration surgery to improve intraocular pressure. Eye

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Allergan Gets FDA Approval For Lumigan 0.01% As First-Line Therapy To Reduce Elevated IOP In Glaucoma Patients – Update

Tuesday, August 31st, 2010

0.01% as a first-line therapy indicated for the reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension. Lumigan or bimatoprost ophthalmic solution 0.01% is an optimized reformulation of Lumigan 0.03%. The

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Allergan, Inc. Receives FDA Approval for LUMIGAN(R) 0.01% as First-Line Therapy Indicated for…

Tuesday, August 31st, 2010

01% as a first-line therapy indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. LUMIGAN(R) 0.01% is an optimized reformulation of LUMIGAN(R) (bimatoprost ophthalmic solution)

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Allergan Gets FDA Approval For LUMIGAN 0.01% As First-line Therapy For Reduction Of Elevated Intraocular Pressure In Glaucoma Patients – Quick Facts

Tuesday, August 31st, 2010

0.01% as a first-line therapy indicated for the reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension. LUMIGAN 0.01% is an optimized reformulation of LUMIGAN 0.03%. LUMIGAN 0.01% is a once-daily

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Allergan, Inc. Receives FDA Approval for LUMIGAN® 0.01% as First-Line Therapy Indicated for the Reduction of Elevated Intraocular Pressure in Glaucoma Patients

Tuesday, August 31st, 2010

01% as a first-line therapy indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. LUMIGAN® 0.01% is an optimized reformulation of LUMIGAN® (bimatoprost ophthalmic solution)

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