Xalatan® 

XALATAN is an ocular hypotensive agent that is believed to reduce intraocular pressure (IOP) by increasing uveoscleral outflow. An estimated 100 million prescriptions for XALATAN have been written worldwide* and it is the most prescribed IOP-lowering agent in the United States.

XALATAN is indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension.

XALATAN has a potent and long-acting IOP-lowering effect without significant long-term drift. Studies showed that XALATAN effectively reduced IOP 24% to 33% in patients with open-angle glaucoma and ocular hypertension. The optimal clinical effect of XALATAN is achieved with daily topical administration. Once-daily administration can enhance patient convenience. Studies show that after 2 years of treatment, XALATAN maintained IOP reduction at the same level with no indication of rising. After 2 years of treatment, only 7% of patients required either additional medication or a switch from XALATAN because of insufficient IOP control (Meta-analysis of three 6-month double-masked trials with 2 open-label extensions in patients with open-angle glaucoma or ocular hypertension treated with XALATAN gd or timolol maleate 0.5% bid for 6 months, then with XALATAN up to 2 years; N= 779 at baseline, n= 113 at 2 years).

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XALATAN is more effective than a combination of timolol plus pilocarpine3 and at least as effective as timolol plus dorzolamide in open-label studies,4,5 indicating that a switch to XALATAN monotherapy can be considered before beginning combination therapy in patients inadequately controlled on beta-adrenergic antagonists. XALATAN can be used concomitantly with other topical ophthalmic agents to lower IOP. If more than one topical agent is used, administer at least 5 minutes apart.

XALATAN has minimal systemic side effects. There are no cardiopulmonary contraindications and no statistically significant effects on heart rate or systolic or diastolic pressure associated with XALATAN. XALATAN has no established association with depression, impotence, or nausea.28, 29

XALATAN can cause changes to pigmented tissues. Most frequently reported are increased pigmentation of the iris, periorbital tissue (eyelid), and eyelashes, and growth of eyelashes. Pigmentation is expected to increase as long as XALATAN is administered; these changes are likely to be permanent and the effects beyond 5 years are not known.

Most common ocular event/signs and symptoms (5% to 15%): blurred vision, burning and stinging, conjunctival hyperemia, foreign body sensation, itching, increased iris pigmentation, and punctate epithelial keratopathy.

XALATAN should be used with caution in patients with a history of intraocular inflammation (iritis/uveitis) and should generally not be used in patients with active intraocular inflammation. XALATAN should be used with caution in aphakic patients, in pseudophakic patients with a torn posterior lens capsule, or in patients with known risk factors for macular edema.

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Xalatan®

 

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