Bausch & Lomb LUMIFY receives FDA approval for eye redness

Bausch & Lomb LUMIFY receives FDA approval for eye redness

December 29, 2017 Source: Sina medicine Author: Kerr

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Clinical studies have shown that 0.025% brimonidine tartrate eye drops achieve 95% symptom improvement in one minute and redness in 8 hours

Bausch & Lomb, the world's leading eye care company, today announced that the US Food and Drug Administration (FDA) has approved LUMIFYTM (0.025% brimonidine tartrate eye drops) as a low-dose brimonidine tartrate. The first and only over-the-counter (OTC) eye drop is used to treat eye redness. Brimonidine was first approved by the FDA in 1996 to reduce intraocular pressure (IOP) in glaucoma patients, with higher doses in prescription ophthalmic care products.

Bausch & Lomb is a wholly-owned subsidiary of Valeant, and Joseph C. Papa, Chairman and CEO of Valeant, said: “Today LUMIFY is certified, consumers have a new treatment to relieve eye redness. LUMIFY is the first and The only OTC eye drop using low-dose brimonidine. Brimonidine has been clinically proven safe and effective since it was first approved as a prescription drug in 1996. We expect LUMIY to be available in the second quarter of 2018. ”

Redness and swelling of the eyes are common symptoms that can be caused by almost any inflammation of the eyes. Clinically used non-selective redness-relieving eye drops can shrink blood vessels in the eye, causing resistance, loss of efficacy, and even redness and swelling. In contrast, low-dose brimonidine (the active ingredient in LUMIFY) selectively shrinks the intraocular veins, increasing the oxygen supply to surrounding tissues, thereby reducing the potential risk of these side effects.

Dr. Paul Karpecki, MD, director of corneal services at the Kentucky Eye Institute, said: "Patients with red eyes and irritation may experience negative emotions that affect daily life. Reduced redness without side effects of recurrent hyperemia or rapid response, may also Lead to overuse and potential corneal toxicity, but it is still a very exciting option."

The 0.025% product of brimonidine tartrate eye drops was originally developed by Eye Therapies, Inc. and then licensed to Bausch & Lomb.

Article reference source: Bausch & Lomb Receives FDA Approval of LUMIFY

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