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Latanoprostene bunod ophthalmic Side Effects

Medically reviewed by Last updated on Oct 4, 2023.

Applies to latanoprostene bunod ophthalmic: ophthalmic solution.

Serious side effects

Along with its needed effects, latanoprostene bunod ophthalmic may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.

Check with your doctor immediately if any of the following side effects occur while taking latanoprostene bunod ophthalmic:

More common

Less common


Incidence not known

Other side effects

Some side effects of latanoprostene bunod ophthalmic may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.

Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


Incidence not known

For Healthcare Professionals

Applies to latanoprostene bunod ophthalmic: ophthalmic solution.


The most frequently reported side effects were conjunctival hyperemia, eye irritation, eye pain, and instillation site pain.[Ref]


Common (1% to 10%): Conjunctival hyperemia, eye irritation, eye pain, instillation site pain

Frequency not reported: Foreign body sensation, punctate keratitis, vision blurred, conjunctival edema, conjunctival irritation[Ref]

About 0.6% of patients discontinued therapy due to ocular adverse reactions including ocular hyperemia, conjunctival irritation, eye irritation, eye pain, conjunctival edema, vision blurred, punctate keratitis, and foreign body sensation.[Ref]


1. (2017) "Product Information. Vyzulta (latanoprostene bunod ophthalmic)." Bausch and Lomb Americas, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Some side effects may not be reported. You may report them to the FDA.