Prolensa Generic Name & Formulations
Bromfenac 0.07%; oph soln; contains benzalkonium chloride, sulfites.
Post-operative inflammation and reduction of ocular pain following cataract surgery.
Prolensa Dosage and Administration
≥18yrs: 1 drop into the affected eye once daily beginning 1 day prior to surgery, continued on the day of surgery, and through the first 14 days post-op. May be given with other topical ophthalmics (eg, alpha-agonists, beta-blockers, carbonic anhydrase inhibitors, cycloplegics, mydriatics); administer at least 5 mins apart.
<18yrs: not established.
Prolensa Boxed Warnings
Sulfite sensitivity. Asthma. May slow or delay wound healing. Bleeding tendencies. Corneal defects/denervation. Ocular surface diseases. Rheumatoid arthritis. Diabetes. Monitor cornea; discontinue if corneal epithelial breakdown occurs. Risk of corneal adverse events may be increased if used >24hrs before surgery, or beyond 14-days post-op. Contact lenses (remove prior to therapy). Pregnancy (avoid during late pregnancy). Nursing mothers.
Concomitant topical corticosteroids may potentiate healing problems. Caution with concomitant drugs that prolong bleeding time.
Prolensa Adverse Reactions
Anterior chamber inflammation, foreign body sensation, eye pain, photophobia, blurred vision; keratitis, corneal reactions (eg, epithelial breakdown, thinning, erosion, ulceration/perforation).
Prolensa Clinical Trials
Prolensa Patient Counseling