Fluorometholone (Monograph)
Brand names: Flarex, Fluor-Op, FML
Drug class: Corticosteroids
ATC class: S01CA07
VA class: OP300
Chemical name: 9-fluoro-11ß,17-dihydroxy-6α-methylpregna-1,4-diene-3,20-dione
Molecular formula: C24H31FO5
CAS number: 426-13-1
Introduction
A synthetic fluorinated corticosteroid; structurally related to progesterone.a
Uses for Fluorometholone
Ophthalmic Inflammation
Symptomatic relief of corticosteroid-responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe. b c e g
Treatment of chronic anterior uveitisd f and corneal injury from burns or penetration of foreign bodies.d f g
Bacterial Ophthalmic Infections
Used for anti-inflammatory properties in conjunction with appropriate anti-infective therapy in some bacterial infections of the eye;d f g used in fixed combination with sulfacetamide sodium or tobramycin when such combination therapy is indicated.d f If an ophthalmic corticosteroid is used in combination with an ophthalmic anti-infective, weigh benefits against risks.g (See Infections under Cautions.)
Fluorometholone Dosage and Administration
Administration
Ophthalmic Administration
Apply topically to the eye(s) as an ophthalmic ointment or suspension.b c d e f g
Shake suspension vigorously prior to use.b d e f
Avoid contamination of the preparation container.a b c d e f
Do not administer suspensions containing benzalkonium chloride while wearing soft contact lenses.b e (See Advice to Patients.)
Dosage
Available as fluorometholone and fluorometholone acetate, alone or in fixed combination with anti-infectives; dosage of fluorometholone acetate expressed in terms of the salt.b c d e f
Pediatric Patients
Ophthalmic Inflammation
Ophthalmic
Fluorometholone 0.1% suspension: In children ≥2 years of age, instill 1 drop into the conjunctival sac of the affected eye(s) 2–4 times daily.e During initial 24–48 hours, dosage may be increased to 1 drop every 4 hours.e
Fluorometholone 0.25% suspension: In children ≥2 years of age, instill 1 drop into the conjunctival sac of the affected eye(s) 2–4 times daily.h
Fluorometholone 0.1% ointment: In children ≥2 years of age, apply ribbon of ointment (approximately 1.3 cm in length) into the conjunctival sac of the affected eye(s) 1–3 times daily.c May be applied every 4 hours during initial 24–48 hours of therapy.c
If improvement does not occur after 2 days, reevaluate the patient.c e h
Duration of therapy depends on the type and severity of the disease and response to therapy.a Do not discontinue prematurely.a c e h
In chronic conditions, gradually taper the dosage when the drug is discontinued to avoid exacerbation of the disease.a c e h
Bacterial Ophthalmic Infections
Ophthalmic
Fluorometholone and sulfacetamide sodium ophthalmic suspension: In children ≥2 years of age, instill 1 drop into the conjunctival sac of the affected eye(s) 4 times daily.d
Fluorometholone acetate and tobramycin ophthalmic suspension: In children ≥2 years of age, instill 1 or 2 drops into the conjunctival sac of the affected eye(s) every 4–6 hours.f During initial 24–48 hours, dosage may be increased to 1 or 2 drops every 2 hours.f
If improvement does not occur after 2 days, reevaluate the patient.d
Duration of therapy depends on the type and severity of the disease and response to therapy.a Do not discontinue prematurely.a d f
In chronic conditions, gradually taper the dosage when the drug is discontinued to avoid exacerbation of the disease.a d
Adults
Ophthalmic Inflammation
Ophthalmic
Fluorometholone 0.1% suspension: Instill 1 drop into the conjunctival sac of the affected eye(s) 2–4 times daily.e During initial 24–48 hours, dosage may be increased to 1 drop every 4 hours.e
Fluorometholone 0.25% suspension: Instill 1 drop into the conjunctival sac of the affected eye(s) 2–4 times daily.h
Fluorometholone 0.1% ointment: Apply ribbon of ointment (approximately 1.3 cm in length) into the conjunctival sac of the affected eye(s) 1–3 times daily.c May be applied every 4 hours during initial 24–48 hours of therapy.c
Fluorometholone acetate 0.1% suspension: Instill 1 or 2 drops into the conjunctival sac of the affected eye(s) 4 times daily.b During initial 24–48 hours, dosage may be increased to 2 drops every 2 hours.b
If improvement does not occur after 2 days, reevaluate the patient.c e h
Duration of therapy depends on the type and severity of the disease and response to therapy.a Do not discontinue prematurely.a c e h
In chronic conditions, gradually taper the dosage when the drug is discontinued to avoid exacerbation of the disease.a c e h
Bacterial Ophthalmic Infections
Ophthalmic
Fluorometholone and sulfacetamide sodium ophthalmic suspension: Instill 1 drop into the conjunctival sac of the affected eye(s) 4 times daily.d
Fluorometholone acetate and tobramycin ophthalmic suspension: Instill 1 or 2 drops into the conjunctival sac of the affected eye(s) every 4–6 hours.f During initial 24–48 hours, dosage may be increased to 1 or 2 drops every 2 hours.f
If improvement does not occur after 2 days, reevaluate the patient.d
Duration of therapy depends on the type and severity of the disease and response to therapy.a Do not discontinue prematurely.a d f
In chronic conditions, gradually taper the dosage when the drug is discontinued to avoid exacerbation of the disease.a d
Special Populations
No special population dosage recommendations at this time.a b c d e f h
Cautions for Fluorometholone
Contraindications
-
Viral diseases of the cornea and conjunctiva (e.g., epithelial herpes simplex keratitis [dendritic keratitis], vaccinia, varicella).b c d e f g h
-
Known hypersensitivity to fluorometholone, other corticosteroids, or any ingredient in the formulation.b c d e f g h
Warnings/Precautions
Warnings
Ocular Effects
Risk of glaucoma (with damage to optic nerve), defects in visual acuity and fields of vision, and posterior subcapsular cataract formation with prolonged use of corticosteroids.b c d e f g h Use with caution in glaucoma because IOP may increase.b c d e f g h
Average time until IOP increase occurs is longer with fluorometholone than with ophthalmic dexamethasone.b c d e f h
If used for ≥10 days, monitor IOP routinely even though monitoring may be difficult in children and uncooperative patients.c d e f g h
In conditions causing thinning of the cornea or sclera, perforations reported with use of topical corticosteroids.b c d e f g h
Use of high-dose corticosteroids may delay healing.b c e g Use after cataract surgery may delay healing and increase incidence of bleb formation.c d e g h
Infections
See Contraindications under Cautions.
Prolonged use may suppress the host response and thus increase the risk of secondary ocular infections.b c d e f g h
In acute purulent conditions of the eye, corticosteroids may mask infection or enhance existing infection.b c d e f g h
Herpes Simplex
Use of corticosteroids in the treatment of herpes simplex infections other than epithelial herpes simplex keratitis, in which corticosteroids are contraindicated, requires great caution; periodic slit-lamp microscopy is essential.b d c g h
General Precautions
Evaluation of Ocular Condition
Initial prescription or renewal of medication order beyond 8 g of 0.1% ointment or 20 mL of 0.1 or 0.25% suspension should be provided only after examination of the patient with the aid of magnification (e.g., slit lamp biomicroscopy, fluorescein staining where appropriate).c d e h
Reevaluate patient if improvement does not occur after 2 days.c d e h
Fungal Infections
Long-term local corticosteroid application associated with development of fungal infections of the cornea.b c d e f g Consider possibility of fungal infection in patients with persistent corneal ulceration who have been or are receiving corticosteroid therapy.b c d e f g
Use of Fixed Combinations
When fluorometholone or fluorometholone acetate is used in fixed combination with sulfacetamide sodium or tobramycin, consider the cautions, precautions, and contraindications associated with the concomitant agent.d f
Ophthalmic Ointments
Use of ophthalmic ointments may decrease rate of corneal reepithelialization.c g
Specific Populations
Pregnancy
Lactation
Not known whether topical ophthalmic administration of corticosteroids could result in sufficient systemic absorption to produce detectable quantities in milk.b c d e f h
Caution if used in nursing women.b f Most manufacturers recommend that women discontinue nursing or the drug.c d e h
Pediatric Use
Safety and efficacy of fluorometholone alone or in fixed combination with sulfacetamide sodium or fluorometholone acetate in fixed combination with tobramycin not established in children <2 years of age.a c d e f h
Manufacturer states that safety and efficacy of fluorometholone acetate alone have not been established in children of any age.a b
Geriatric Use
No substantial differences in safety or efficacy relative to younger patients.c d e f h
Common Adverse Effects
Elevated IOP,c d e h transient stinging or burning,e g h blurred vision,e g h ocular irritation,e g h taste perversion.e h
Fluorometholone Pharmacokinetics
Absorption
Bioavailability
Corticosteroids are absorbed through the aqueous humor; because only low doses are given, little if any systemic absorption occurs.g
Stability
Storage
Ophthalmic
Ointment
<25°C. c Avoid exposure to temperatures >40°C. c
Suspension
Fluorometholone or fluorometholone acetate suspension: 2–27°C.a b Do not freeze. a b
Fluorometholone and sulfacetamide sodium suspension: Light-protected container at 15–30°C.d Do not freeze.d Do not use suspension if dark brown. d
Fluorometholone acetate and tobramycin suspension: Upright at 2–25°C.f
Compatibility
Ophthalmic
Suspension
Fluorometholone and sulfacetamide sodium suspension: Incompatible with preparations containing silver.d
Actions
-
Corticosteroids suppress the inflammatory response to mechanical, chemical, or immunologic agents.b c d e f g h
-
Corticosteroids inhibit edema, fibrin deposition, capillary dilation, leukocyte migration, capillary proliferation, fibroblast proliferation, deposition of collagen, and scar formation associated with inflammation.c d e g h
Advice to Patients
-
Importance of discontinuing therapy and consulting a clinician if inflammation or pain persists for >48 hours or worsens.c d e h
-
Importance of removing soft contact lenses prior to administering preparations containing benzalkonium chlorideb e and of delaying reinsertion of the lenses for ≥15 minutes after administration.e
-
Importance of learning and adhering to proper administration techniques to avoid contamination of the tip of the container.b c d e f h
-
Importance of warning the patient not to share the drug.c d e h
-
Importance of informing a clinician if an intercurrent ocular condition (e.g., trauma, surgery, infection) develops during ophthalmic therapy.g
-
Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs, as well as any concomitant illnesses.c d e f h
-
Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.c d e f h
-
Importance of informing patients of other important precautionary information.b c d e f g h (See Cautions.)
Preparations
Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.
Please refer to the ASHP Drug Shortages Resource Center for information on shortages of one or more of these preparations.
Routes |
Dosage Forms |
Strengths |
Brand Names |
Manufacturer |
---|---|---|---|---|
Ophthalmic |
Ointment |
0.1% |
FML (with phenylmercuric acetate) |
Allergan |
Suspension |
0.1% |
Fluor-Op (with benzalkonium chloride) |
Novartis |
|
Fluorometholone Ophthalmic Suspension |
Bausch & Lomb |
|||
FML (with benzalkonium chloride) |
Allergan |
|||
0.25% |
FML Forte (with benzalkonium chloride) |
Allergan |
Routes |
Dosage Forms |
Strengths |
Brand Names |
Manufacturer |
---|---|---|---|---|
Ophthalmic |
Suspension |
0.1% with Sulfacetamide Sodium 10% |
FML-S Liquifilm (with benzalkonium chloride and povidone) |
Allergan |
Routes |
Dosage Forms |
Strengths |
Brand Names |
Manufacturer |
---|---|---|---|---|
Ophthalmic |
Suspension |
0.1% |
Flarex (with benzalkonium chloride) |
Alcon |
Routes |
Dosage Forms |
Strengths |
Brand Names |
Manufacturer |
---|---|---|---|---|
Ophthalmic |
Suspension |
0.1% with Tobramycin 0.3% |
Tobraflex (with benzalkonium chloride) |
Alcon |
AHFS DI Essentials™. © Copyright 2025, Selected Revisions September 1, 2007. American Society of Health-System Pharmacists, Inc., 4500 East-West Highway, Suite 900, Bethesda, Maryland 20814.
References
a. AHFS drug information 2007. McEvoy GK, ed. Fluorometholone. Bethesda, MD: American Society of Health-Systems Pharmacists; 2007: 2825.
b. Alcon Laboratories, Inc. Flarex (fluorometholone acetate) suspension prescribing information. Fort Worth , TX; 1999 Jun.
c. Allergan, Inc. FML (fluorometholone) ointment prescribing information. Irvine, CA; 2001 Nov.
d. Allergan, Inc. FML-S (fluorometholone and sulfacetamide sodium) suspension prescribing information. Irvine, CA; 2005 Feb.
e. Allergan, Inc. FML (fluorometholone) ophthalmic suspension, 0.1% prescribing information. Irvine, CA; 2003 Jun.
f. Alcon Pharmaceuticals. Tobraflex (tobramycin and fluorometholone acetate) suspension prescribing information. Fort Worth, TX; 2001 May.
g. AHFS drug information 2007. McEvoy GK,ed. EENT corticosteroids general statement. Bethesda, MD: American Society of Health Systems Pharmacists; 2007: 2813-5.
h. Allergan, Inc. FMLForte(fluorometholone) suspension prescribing information. Irvine, CA; 2004 Jun.
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