Flurbiprofen Sodium Drug Information
Generic name: FLURBIPROFEN SODIUM
Uses of Flurbiprofen Sodium
Flurbiprofen sodium ophthalmic solution is indicated for the inhibition of intraoperative miosis.
Dosage & Administration of Flurbiprofen Sodium
A total of four drops of flurbiprofen sodium ophthalmic solution should be administered by instilling one drop approximately every 1/2 hour beginning 2 hours before surgery.
Side Effects of Flurbiprofen Sodium
Transient burning and stinging upon instillation and other minor symptoms of ocular irritation have been reported with the use of flurbiprofen sodium ophthalmic solution. Other adverse reactions reported with the use of flurbiprofen sodium ophthalmic solution include: fibrosis, hyphema, miosis, mydriasis, and ocular hyperemia. Increased bleeding tendency of ocular tissues in conjunction with ocular surgery has also been reported.
To report SUSPECTED ADVERSE REACTIONS, contact Bausch & Lomb Incorporated at 1-800-553-5340 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Warnings & Cautions for Flurbiprofen Sodium
With some nonsteroidal anti-inflammatory drugs, there exists the potential for increased bleeding time due to interference with thrombocyte aggregation. There have been reports that flurbiprofen sodium ophthalmic solution may cause increased bleeding of ocular tissues (including hyphemas) in conjunction with ocular surgery. There is the potential for cross-sensitivity to acetylsalicylic acid and other nonsteroidal anti-inflammatory drugs.
Therefore, caution should be used when treating individuals who have previously exhibited sensitivities to these drugs.
Drug Interactions with Flurbiprofen Sodium
Drug Interactions Interaction of flurbiprofen sodium ophthalmic solution with other topical ophthalmic medications has not been fully investigated. Although clinical studies with acetylcholine chloride and animal studies with acetylcholine chloride or carbachol revealed no interference, and there is no known pharmacological basis for an interaction, there have been reports that acetylcholine chloride and carbachol have been ineffective when used in patients treated with flurbiprofen sodium ophthalmic solution.
Pregnancy Safety for Flurbiprofen Sodium
Pregnancy Flurbiprofen has been shown to be embryocidal, delay parturition, prolong gestation, reduce weight, and/or slightly retard growth of fetuses when given to rats in daily oral doses of 0.4 mg/kg (approximately 300 times the human daily topical dose) and above. There are no adequate and well-controlled studies in pregnant women. Flurbiprofen sodium ophthalmic solution should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.
Pediatric Use of Flurbiprofen Sodium
Pediatric Use Safety and effectiveness in pediatric patients have not been established.
Contraindications for Flurbiprofen Sodium
Flurbiprofen sodium ophthalmic solution is contraindicated in individuals who are hypersensitive to any components of the medication.
Overdosage Information for Flurbiprofen Sodium
Overdosage will not ordinarily cause acute problems. If accidentally ingested, drink fluids to dilute.
Drug information sourced from the FDA. This content is for informational purposes only and does not constitute medical advice. Consult a healthcare professional before making any medication decisions.
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