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Bromday (bromfenac ophthalmic solution) 0.09% is indicated for the treatment of postoperative inflammation and reduction of ocular pain in patients who have undergone cataract surgery.
DOSAGE AND ADMINISTRATION
For the treatment of postoperative inflammation in patients who have undergone cataract extraction, one drop of Bromday (bromfenac ophthalmic solution) ophthalmic solution should be applied to the affected eye(s) once daily beginning 1 day prior to cataract surgery, continued on the day of surgery, and through the first 14 days of the postoperative period.
Use with Other Topical Ophthalmic Medications
Bromday (bromfenac ophthalmic solution) ophthalmic solution may be administered in conjunction with other topical ophthalmic medications such as alpha-agonists, beta-blockers, carbonic anhydrase inhibitors, cycloplegics, and mydriatics. Drops should be administered at least 5 minutes apart.
Dosage Forms And Strengths
Topical ophthalmic solution: bromfenac 0.09%.
Bromday (bromfenac ophthalmic solution) 0.09% is supplied in a white LDPE plastic squeeze bottle with a 15 mm LDPE white dropper-tip and 15 mm polypropylene gray cap as follows:
1.7 ml in 7.5 ml container (NDC 67425-999- 17)
Store at 155° - 255°C (595° - 77°F).
Manufactured for: ISTA Pharmaceuticals, Inc. Irvine, CA 92618. Manufactured By: Bausch & Lomb Incorporated Tampa, FL 33637. Under license from: Senju Pharmaceuticals Co., Ltd. Osaka, Japan 541-0046. Revised: 9/2010
Last reviewed on RxList: 11/15/2010
This monograph has been modified to include the generic and brand name in many instances.
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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