FML-S Liquifilm Side Effects
Generic name: fluorometholone / sulfacetamide sodium ophthalmic
Note: This document contains side effect information about fluorometholone / sulfacetamide sodium ophthalmic. Some of the dosage forms listed on this page may not apply to the brand name FML-S Liquifilm.
Ocular side effects associated with the fluorometholone component have included burning and stinging upon instillation, ocular irritation, visual disturbances, elevation of intraocular pressure with possible development of glaucoma, visual field defects, posterior subcapsular cataract formation, delayed wound healing, and optic nerve damage. Corticosteroid containing preparations have also been reported to cause acute anterior uveitis, perforation of the globe, keratitis, conjunctivitis, corneal ulcers, mydriasis, conjunctival hyperemia, loss of accommodation, and ptosis.
Local irritation, stinging, and burning have been reported with the use of sodium sulfacetamide.[Ref]
Fluorometholone ophthalmic has caused the development of secondary ocular infections.[Ref]
Hypersensitivity reactions to sodium sulfacetamide have been reported rarely. A case of Stevens Johnson syndrome has been reported in a patient who had previously experienced a bullous drug reaction to an orally administered sulfonamide. A case of local hypersensitivity which progressed to a fatal syndrome resembling systemic lupus erythematosus has also been reported.[Ref]
Gastrointestinal side effects have included taste perversion.[Ref]
More about FML-S Liquifilm (fluorometholone / sulfacetamide sodium ophthalmic)
- During Pregnancy
- Dosage Information
- Drug Interactions
- Drug class: ophthalmic steroids with anti-infectives
Related treatment guides
1. "Product Information. FML Ophthalmic Suspension (fluoromethalone ophthalmic)." Allergan Inc, Irvine, CA.
2. "Product Information. Sulamyd Ophthalmic Solution (sodium sulfacetamide ophthalmic)." Schering Corporation, Kenilworth, NJ.
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Some side effects may not be reported. You may report them to the FDA.