"The U.S. Food and Drug Administration today warned five eye care providers to stop the misleading advertising and promotion of refractive lasers used in eye surgery procedures such as LASIK. The FDA found that the providers’ advertisements "...
Clinical Trial Experience
The most commonly reportaed adverse experiences reported following use of bromfenac after cataract surgery include: abnormal sensation in eye, conjunctival hyperemia, eye irritation (including burning/stinging), eye pain, eye pruritus, eye redness, headache, and iritis. These events were reported in 2-7% of patients.
The following events have been identified during post-marketing use of bromfenac ophthalmic solution 0.09% in clinical practice. Because they are reported voluntarily from a population of unknown size, estimates of frequency cannot be made. The events, which have been chosen for inclusion due to either their seriousness, frequency of reporting, possible causal connection to topical
bromfenac ophthalmic solution 0.09% or a combination of these factors, include corneal erosion, corneal perforation, corneal thinning, and epithelial breakdown, [see WARNINGS AND PRECAUTIONS]
Read the Bromday (bromfenac ophthalmic solution) Side Effects Center for a complete guide to possible side effects
Last reviewed on RxList: 11/15/2010
Additional Bromday Information
- Bromday Drug Interactions Center: bromfenac opht
- Bromday Side Effects Center
- Bromday Overview including Precautions
- Bromday FDA Approved Prescribing Information including Dosage
Bromday - User Reviews
Bromday User Reviews
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Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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