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Xibrom

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Xibrom

Xibrom Side Effects Center

Medical Editor: John P. Cunha, DO, FACOEP

Xibrom (bromfenac ophthalmic solution) is used to treat swelling and pain caused by cataract surgery. It is a nonsteroidal anti-inflammatory drug (NSAID). Common side effects include temporary irritation/burning/stinging of the eye, temporary blurred vision, watery eyes, or headache.

For the treatment of postoperative inflammation in patients who have undergone cataract extraction, the recommended dose of Xibrom ophthalmic solution is one drop applied to the affected eye(s) two times daily beginning 24 hours after cataract surgery and continuing through the first 2 weeks of the postoperative period. Xibrom may interact with steroids. Other drugs may interact with Xibrom ophthalmic. Tell your doctor all prescription and over-the-counter medications and supplements you use. During pregnancy, Xibrom should be used only when prescribed. It is not recommended for use during the last 3 months of pregnancy due to possible harm to a fetus and interference with normal labor/delivery. It is unknown if this drug passes into breast milk. Consult your doctor before breastfeeding.

Our Xibrom (bromfenac ophthalmic solution) Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What is Patient Information in Detail?

Easy-to-read and understand detailed drug information and pill images for the patient or caregiver from Cerner Multum.

Xibrom in Detail - Patient Information: Side Effects

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat.

Stop using bromfenac ophthalmic and call your doctor at once if you have a serious side effect such as:

  • any change in your vision;
  • slow healing after your eye surgery;
  • eye redness or bleeding;
  • eye pain or swelling, increased sensitivity to light;
  • feeling like something is in your eye; or
  • severe eye discomfort, increased tears, crusting or drainage.

Less serious side effects may include:

  • mild burning or stinging when you apply the eye drops;
  • eye itching;
  • headache; or
  • seeing flashes of light or "floaters" in your vision.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

Read the entire detailed patient monograph for Xibrom (Bromfenac Ophthalmic Solution ) »

What is Patient Information Overview?

A concise overview of the drug for the patient or caregiver from First DataBank.

Xibrom Overview - Patient Information: Side Effects

SIDE EFFECTS: Temporary irritation/burning/stinging of the eye, temporary blurred vision, watery eyes, or headache may occur. If any of these effects persist or worsen, tell your doctor or pharmacist promptly.

Remember that your doctor has prescribed this medication because he or she has judged that the benefit to you is greater than the risk of side effects. Many people using this medication do not have serious side effects.

Tell your doctor immediately if any of these unlikely but serious side effects occur: severe pain/redness in the eye, sensitivity of the eyes to light (photophobia), eye discharge, blurry/abnormal vision, feeling as if something is in the eye, itching/redness/pain around the eyes.

A very serious allergic reaction to this drug is rare. However, seek immediate medical attention if you notice any of the following symptoms of a serious allergic reaction: rash, itching/swelling (especially of the face/tongue/throat), severe dizziness, trouble breathing.

If you notice other effects not listed above, contact your doctor or pharmacist.

In the US -

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.

Read the entire patient information overview for Xibrom (Bromfenac Ophthalmic Solution )»

What is Prescribing information?

The FDA package insert formatted in easy-to-find categories for health professionals and clinicians.

Xibrom FDA Prescribing Information: Side Effects
(Adverse Reactions)

SIDE EFFECTS

Clinical Trial Experience

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.

The most commonly reported adverse reactions 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 reactions were reported in 2 to 7% of patients.

Post-Marketing Experience

The following reactions 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 reactions, 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 entire FDA prescribing information for Xibrom (Bromfenac Ophthalmic Solution ) »

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Xibrom - User Reviews

Xibrom User Reviews

Now you can gain knowledge and insight about a drug treatment with Patient Discussions.

Here is a collection of user reviews for the medication Xibrom sorted by most helpful. Patient Discussions FAQs

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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