December 28, 2017
1 min read
Save

FDA approves Bausch + Lomb’s Lumify for ocular redness

You've successfully added to your alerts. You will receive an email when new content is published.

Click Here to Manage Email Alerts

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com.

The FDA approved Bausch + Lomb’s Lumify as the first over-the-counter eye drop developed with low-dose brimonidine tartrate for the treatment of ocular redness.

Perspective from Arthur A. Medina Jr. , OD

Brimonidine was first approved by the FDA in 1996 for the reduction of IOP in glaucoma patients, according to a press release from Valeant Pharmaceuticals.

“Lumify is the first and only OTC eye drop with low-dose brimonidine, which has been clinically proven to be safe and effective since its initial approval as a prescription medication in 1996,” Joseph C. Papa, chairman and CEO of Valeant, said in the release.

Lumify (brimonidine tartrate ophthalmic solution 0.025%) is expected to be available in the second quarter of 2018.

Frequent use of non-selective redness-relieving eye drops that constrict blood vessels in the eye may cause patients to develop a tolerance or loss of effectiveness. Low-dose brimonidine can lower this risk by selectively constricting veins in the eyes and increasing the availability of oxygen to the surrounding eye tissues, the release said.