Dexamethasone (EENT) (Monograph)
Brand name: Maxidex
Drug class: Corticosteroids
Dexamethasone (EENT) is also contained as an ingredient in the following combinations:
Neomycin and Polymyxin B Sulfates and Dexamethasone
Introduction
A synthetic fluorinated corticosteroid.
Uses for Dexamethasone (EENT)
Ophthalmic Inflammation
Symptomatic relief of corticosteroid-responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe (e.g., allergic conjunctivitis, acne rosacea, superficial punctate keratitis, herpes zoster keratitis, iritis, cyclitis, selected infective conjunctivitides).
Treatment of chronic anterior uveitis.
Treatment of corneal injury from chemical, radiation, or thermal burns or penetration of foreign bodies.
Bacterial Ophthalmic Infections
Used for anti-inflammatory properties in conjunction with appropriate anti-infective therapy in some bacterial infections of the eye; used in fixed combination with neomycin and polymyxin B sulfates or tobramycin when such combination therapy is indicated. If an ophthalmic corticosteroid is used in combination with an ophthalmic anti-infective, weigh benefits against risks. (See Infections under Cautions.)
Otic Inflammation
Symptomatic relief of corticosteroid-responsive inflammatory conditions of the ear canal (e.g., allergic otitis externa).
Bacterial Otic Infections
Used for anti-inflammatory properties in conjunction with ciprofloxacin for treatment of acute otitis externa and in pediatric patients with tympanostomy tubes for acute otitis media.
Used to reduce edema and inflammation in select cases of purulent and nonpurulent infective otitis externa.
If a corticosteroid is used alone or in combination with an otic anti-infective, weigh benefits against risks. (See Infections under Cautions.)
Dexamethasone (EENT) Dosage and Administration
Administration
Apply topically to the eye or ear.
Ophthalmic Administration
Apply topically to the eye as an ophthalmic ointment, solution, or suspension.
Not for injection.
Shake suspension well prior to each use.
Avoid contamination of preparation container.
Do not administer solutions or suspensions containing benzalkonium chloride while wearing soft contact lenses. Wait ≥15 minutes after instilling drops before inserting contact lenses. (See Advice to Patients.)
Otic Administration
Apply topically to the ear as an otic suspension or an ophthalmic solution.
Not for injection. Do not instill otic preparations into the eye.
May use dexamethasone sodium phosphate ophthalmic solution in the ear.
Shake suspension well prior to each use.
To avoid dizziness that may result from instilling a cold preparation into the ear, warm the preparation by holding the bottle in the hands for 1–2 minutes prior to administration.
Clean and dry ear canal prior to administration; pH of otic preparations should be neutral or acidic.
Lie with the affected ear upward and instill drops. For pediatric patients with otitis media and tympanostomy tubes, pump the tragus 5 times to ease penetration of drops into the middle ear. For acute otitis externa, pull outer ear lobe upward and backward to facilitate entry of drug into ear canal.
Keep affected ear upward for ≥60 seconds following drug administration. If necessary, repeat procedure for the opposite ear.
Use otic corticosteroids sparingly to prevent an accumulation of excess debris in the ear canal.
Dosage
Commercially available alone or in fixed combination with anti-infectives; available as dexamethasone or dexamethasone sodium phosphate. Solution available as dexamethasone sodium phosphate; dosage expressed in terms of dexamethasone phosphate.
Pediatric Patients
Bacterial Ophthalmic Infections
Duration of therapy depends on the type and severity of the disease and response to therapy. Do not discontinue prematurely.
When discontinuing therapy, gradually taper dosing frequency to avoid exacerbation of the disease.
Dexamethasone 0.1% and Tobramycin 0.3%
Ophthalmic SuspensionChildren ≥2 years of age: Initial 24–48 hours, 1 or 2 drop(s) into the conjunctival sac of the affected eye(s) every 2 hours. Thereafter, 1 or 2 drops every 4–6 hours. Gradually reduce dosing frequency as infection improves.
Ophthalmic OintmentChildren ≥2 years of age: Apply a 1.25-cm ribbon into the conjunctival sac of the affected eye(s) up to 3 or 4 times daily.
Bacterial Otic Infections
Acute Otitis Externa
Otic Suspension (Dexamethasone 0.1% and Ciprofloxacin 0.3%)Children ≥6 months of age: 4 drops into the affected ear(s) twice daily for 7 days.
Acute Otitis Media
Otic Suspension (Dexamethasone 0.1% and Ciprofloxacin 0.3%)Children ≥6 months of age with tympanostomy tubes: 4 drops into the affected ear(s) twice daily for 7 days.
Adults
Ophthalmic Inflammation and Bacterial Infections
Duration of therapy depends on the type and severity of the disease and response to therapy. Do not discontinue prematurely.
When discontinuing therapy, gradually taper dosing frequency to avoid exacerbation of the disease.
Dexamethasone 0.1%
Ophthalmic SuspensionFor mild inflammation: 1 or 2 drops into the conjunctival sac of the affected eye(s) up to 4–6 times daily.
For severe inflammation: 1 or 2 drops into the conjunctival sac of the affected eye(s) every hour. Taper dosing frequency as inflammation subsides.
Dexamethasone Sodium Phosphate 0.1%
Ophthalmic SolutionInitially, 1 or 2 drops into the conjunctival sac of the affected eye(s) every hour during the day and every 2 hours during the night. When a favorable response is attained, decrease to 1 drop every 4 hours. May decrease to 1 drop 3 or 4 times daily to control symptoms.
Dexamethasone 0.1%, Neomycin 0.35%, and Polymyxin B Sulfates 10,000 units
Ophthalmic SuspensionFor mild inflammation: 1 or 2 drop(s) into the conjunctival sac of the affected eye(s) up to 4–6 times daily.
For severe inflammation: 1 or 2 drops into the conjunctival sac of the affected eye(s) hourly. As inflammation subsides, gradually reduce dosing frequency to discontinue.
Ophthalmic OintmentApply a 1.25-cm ribbon into the conjunctival sac of the affected eye(s) up to 3 or 4 times daily.
Dexamethasone 0.1% and Tobramycin 0.3%
Ophthalmic SuspensionInitial 24–48 hours, 1 or 2 drops into the conjunctival sac of the affected eye(s) every 2 hours; thereafter, 1 or 2 drops every 4 to 6 hours. Gradually reduce dosing frequency as infection improves.
Ophthalmic OintmentApply a 1.25-cm ribbon into the conjunctival sac of the affected eye(s) up to 3 or 4 times daily.
Otic Inflammation
Dexamethasone Sodium Phosphate 0.1% Ophthalmic Solution
OticInitially, 3 or 4 drops of the ophthalmic solution into the ear canal 2 or 3 times daily. May reduce dosing frequency as symptoms improve. Gradually taper the drug when it is discontinued.
Alternatively, a cotton wick saturated with the ophthalmic solution may be packed into the ear canal; keep the wick moist with the ophthalmic solution; remove saturated wick from ear after 12 to 24 hours. Repeat as necessary.
Duration of treatment may range from a few days to several weeks.
Bacterial Otic Infections: Acute Otitis Externa
Dexamethasone 0.1% and Ciprofloxacin 0.3%
Otic4 drops into the affected ear(s) twice daily for 7 days.
Special Populations
No special population dosage recommendations at this time.
Cautions for Dexamethasone (EENT)
Contraindications
-
Known hypersensitivity to dexamethasone or any ingredient in the formulation.
- Ophthalmic Preparations
-
Viral diseases of the cornea and conjunctiva (e.g., epithelial herpes simplex keratitis [dendritic keratitis], vaccinia, varicella).
-
Mycobacterial infection (e.g., ocular tuberculosis) of the eye.
-
Fungal disease of ocular structures.
- Otic Preparations
-
Viral infections of the external ear canal (e.g., herpes simplex).
-
Perforation of the ear drum.
-
Fungal diseases of auricular structures.
Warnings/Precautions
Warnings
Ocular Effects
Risk of glaucoma with possible damage to the optic nerve, defects in visual acuity and fields of vision, and posterior subcapsular cataract formation with prolonged use of corticosteroids. Use with caution in patients with glaucoma because IOP may increase.
If used for ≥10 days, monitor IOP routinely even though monitoring may be difficult in children and uncooperative patients.
In conditions causing thinning of the cornea or sclera, perforations reported with use of topical corticosteroids.
Use of high-dose corticosteroids may delay healing. Use after cataract surgery may delay healing and increase incidence of bleb formation.
Infections
Prolonged use may suppress the host response and thus increase the risk of secondary ocular infections.
In acute purulent conditions of the eye or ear, corticosteroids may mask infection or enhance existing infection. (See Contraindications under Cautions.)
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.
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% suspension should be provided only after examination of the patient with the aid of magnification (e.g., slit lamp biomicroscopy, fluorescein staining where appropriate).
Fungal Infections
Long-term local corticosteroid application associated with development of fungal infections of the cornea. Consider possibility of fungal infection in patients with persistent corneal ulceration who have been or are receiving corticosteroid therapy.
Corneal Reepithelialization
Use of ophthalmic ointments may decrease rate of corneal reepithelialization.
Use of Fixed Combination
When used in fixed combination with ciprofloxacin, neomycin and polymyxin B sulfates, or tobramycin, consider the cautions, precautions, and contraindications associated with the concomitant agents.
Specific Populations
Pregnancy
Category C.
Lactation
Not known whether topical administration of corticosteroids could result in sufficient systemic absorption to produce detectable quantities in milk.
Caution if used in nursing women.
Dexamethasone sodium phosphate ophthalmic solution and dexamethasone in fixed combination with ciprofloxacin otic suspension: Manufacturers recommend discontinuing nursing or the drug.
Pediatric Use
Safety and efficacy of ophthalmic dexamethasone suspension or dexamethasone sodium phosphate solution not established.
Safety and efficacy of ophthalmic dexamethasone in fixed combination with neomycin and polymyxin B sulfates not established.
Safety and efficacy of ophthalmic dexamethasone in fixed combination with tobramycin not established in children <2 years of age.
Safety and efficacy of otic dexamethasone suspension in fixed combination with ciprofloxacin not established in infants <6 months of age.
Geriatric Use
No substantial differences in safety or efficacy relative to younger patients.
Common Adverse Effects
Ophthalmic administration: Elevated IOP, posterior subcapsular cataract formation, optic nerve damage, delayed wound healing.
Otic administration: Ear discomfort, ear pain, ear pruritus.
Dexamethasone (EENT) Pharmacokinetics
Absorption
Bioavailability
Corticosteroids are absorbed through the aqueous humor; because only low doses are given, little if any systemic absorption occurs after ophthalmic administration.
Distribution
Extent
Systemically absorbed corticosteroids are distributed into milk; not known whether topical corticosteroids could produce detectable levels in human milk.
Stability
Storage
Ophthalmic
Ointment
Neomycin and polymyxin B sulfates and dexamethasone: 2–25°C.
Tobramycin and dexamethasone: 8–27°C.
Solution
Dexamethasone sodium phosphate: 15–30°C.
Suspension
Dexamethasone: Tight, light-resistant containers at 8–27°C; store upright.
Neomycin and polymyxin B sulfates and dexamethasone: 8–27°C.
Tobramycin and dexamethasone: Upright containers at 8–27°C.
Otic
Suspension
Ciprofloxacin and dexamethasone: 15–30°C; protect from light. Do not freeze.
Actions
-
Corticosteroids suppress the inflammatory response to mechanical, chemical, or immunologic agents.
-
Corticosteroids inhibit edema, fibrin deposition, capillary dilation, leukocyte and phagocyte migration; in addition, the drugs reduce capillary proliferation, fibroblast proliferation, deposition of collagen, and scar formation associated with inflammation.
Advice to Patients
-
Importance of removing soft contact lenses prior to administering preparations containing benzalkonium chloride and of delaying reinsertion of the lenses for ≥15 minutes after administration. Importance of not wearing contact lenses if signs or symptoms of an eye infection occur.
-
Importance of learning and adhering to proper administration techniques to avoid contamination of the tip of the container.
-
Importance of advising patients not to touch tip of dropper to eye or surrounding tissue.
-
Importance of informing a clinician if another eye condition (e.g., trauma, surgery, infection) develops during ophthalmic therapy.
-
Advise patients to warm the ear suspension by holding the bottle in the hands for 1–2 minutes prior to administration.
-
Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs as well as any concomitant illnesses.
-
Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.
-
Importance of informing patients of other important precautionary information. (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 |
Suspension |
0.1% |
Maxidex (with benzalkonium chloride; viscous) |
Alcon |
Routes |
Dosage Forms |
Strengths |
Brand Names |
Manufacturer |
---|---|---|---|---|
Otic |
Suspension |
Ciprofloxacin 0.3% and Dexamethasone 0.1% per mL |
Ciprodex (with benzalkonium chloride) |
Alcon |
* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name
Routes |
Dosage Forms |
Strengths |
Brand Names |
Manufacturer |
---|---|---|---|---|
Ophthalmic |
Ointment |
Neomycin Sulfate 0.35% (of neomycin), Polymyxin B Sulfate 10,000 units (of polymyxin B) and Dexamethasone 0.1% per g* |
Maxitrol |
Alcon |
Neomycin and Polymyxin B Sulfates and Dexamethasone |
Bausch & Lomb |
|||
Suspension |
Neomycin Sulfate 0.35% (of neomycin), Polymyxin B Sulfate 10,000 units (of polymyxin B) and Dexamethasone 0.1% per mL* |
Maxitrol (with benzalkonium chloride; viscous) |
Alcon |
|
Neomycin and Polymyxin B Sulfates and Dexamethasone |
Bausch & Lomb |
Routes |
Dosage Forms |
Strengths |
Brand Names |
Manufacturer |
---|---|---|---|---|
Ophthalmic |
Ointment |
0.3% Tobramycin and Dexamethasone 0.1% per g |
TobraDex (with chlorobutanol) |
Alcon |
Suspension |
0.3% Tobramycin and Dexamethasone 0.1% per mL |
TobraDex (with benzalkonium chloride) |
Alcon |
* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name
Routes |
Dosage Forms |
Strengths |
Brand Names |
Manufacturer |
---|---|---|---|---|
Ophthalmic |
Solution |
0.1% (of dexamethasone phosphate)* |
Dexamethasone Sodium Phosphate (with benzalkonium chloride) |
Falcon |
AHFS DI Essentials™. © Copyright 2025, Selected Revisions April 1, 2010. American Society of Health-System Pharmacists, Inc., 4500 East-West Highway, Suite 900, Bethesda, Maryland 20814.