Omidria Side Effects
Generic name: ketorolac / phenylephrine ophthalmic
Medically reviewed by Drugs.com. Last updated on Sep 21, 2022.
Note: This document contains side effect information about ketorolac / phenylephrine ophthalmic. Some dosage forms listed on this page may not apply to the brand name Omidria.
Serious side effects of Omidria
Check with your doctor or nurse immediately if any of the following side effects occur while taking ketorolac/phenylephrine ophthalmic:
- Decreased vision or other changes in vision
- loss of vision
Get emergency help immediately if any of the following symptoms of overdose occur while taking ketorolac/phenylephrine ophthalmic:
Symptoms of overdose
- fast, pounding, or irregular heartbeat or pulse
- fear or nervousness
Other side effects of Omidria
Some side effects of ketorolac / phenylephrine 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:
- Feeling of having something in the eye
- red, sore eyes
For Healthcare Professionals
Applies to ketorolac / phenylephrine ophthalmic: intraocular solution.
Very common (10% or more): Anterior chamber inflammation (24%)
Common (1% to 10%): Increased intraocular pressure, posterior capsule opacification, eye irritation, foreign body sensation in the eyes[Ref]
More about Omidria (ketorolac / phenylephrine ophthalmic)
- Check interactions
- Pricing & coupons
- Dosage information
- During pregnancy
- FDA approval history
- Drug class: ophthalmic surgical agents
Related treatment guides
1. "Product Information. Omidria (ketorolac-phenylephrine ophthalmic)." Omeros Corporation (2014):
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.