Dexamethasone eye drops are a potent ophthalmic corticosteroid formulation used for the treatment of inflammatory conditions affecting the anterior segment of the eye. They are intended for short-term use due to the risk of ocular complications such as elevated intraocular pressure (IOP), glaucoma, or cataract formation. This ophthalmic preparation exerts powerful anti-inflammatory effects locally, reducing symptoms such as redness, swelling, pain, and irritation associated with ocular inflammation.
Pharmacological Classification
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Therapeutic class: Ophthalmic anti-inflammatory agent
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Pharmacological class: Glucocorticoid (corticosteroid)
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ATC code: S01BA01
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Regulatory status: Prescription-only (Rx)
Mechanism of Action
Dexamethasone, as a fluorinated synthetic glucocorticoid, inhibits multiple inflammatory pathways in the eye. Its mechanism includes:
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Suppression of prostaglandin and leukotriene synthesis via inhibition of phospholipase A2
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Downregulation of inflammatory cytokines and adhesion molecules
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Stabilization of lysosomal membranes
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Reduction in capillary permeability and leukocyte infiltration
This leads to a pronounced anti-inflammatory effect, especially useful in treating both non-infectious and post-surgical ocular inflammations.
Formulations and Brand Names
Typical Formulation
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Concentration: 0.1% dexamethasone phosphate (equivalent to 1 mg/mL)
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Form: Sterile ophthalmic suspension or solution
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Packaging: Dropper bottles (typically 5 mL or 10 mL)
Common Brands
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Maxidex® (Alcon) – suspension
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Dexafree® – preservative-free single-dose units
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Ozadex® (intravitreal implant, different route) – for posterior segment inflammation
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Tobradex® – combination of dexamethasone + tobramycin (antibiotic)
Indications
Dexamethasone eye drops are indicated in:
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Non-infectious anterior uveitis and iritis
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Postoperative ocular inflammation (e.g. after cataract or laser surgery)
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Conjunctivitis (non-infectious allergic or irritative)
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Keratitis (non-infectious forms)
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Episcleritis and scleritis (mild to moderate)
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Corneal injury due to chemicals, radiation, or thermal burns
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Foreign body reactions
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Severe allergic conjunctivitis
Not used in primary infectious eye diseases unless under close supervision and combined with antimicrobials.
Dosing and Administration
Typical Adult Dose
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1 to 2 drops into the affected eye(s) every 4 to 6 hours
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In more severe inflammation: 1 to 2 drops hourly during initial treatment
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Tapering: Once inflammation is controlled, frequency is gradually reduced
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Maximum duration: Should not exceed 7–14 days unless under ophthalmic supervision
Pediatric Use
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Can be used with caution under specialist direction
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Dosing frequency and duration should be limited to the lowest effective schedule
Administration Advice
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Shake bottle well if using suspension formulations
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Instill into the conjunctival sac, not directly on the cornea
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Close eyelids gently for 1–2 minutes after instillation
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Wait at least 5 minutes between different eye medications
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Avoid contact lenses during treatment (especially with preserved products)
Contraindications
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Active ocular viral infections: Herpes simplex keratitis (dendritic), varicella
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Ocular fungal infections
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Acute purulent or untreated bacterial conjunctivitis or blepharitis
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Tuberculosis of the eye
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Hypersensitivity to dexamethasone or formulation components
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Unhealed corneal epithelial defects
Precautions and Monitoring
Ocular Monitoring
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Intraocular pressure (IOP) monitoring during prolonged use (especially in glaucoma patients)
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Periodic slit-lamp and fundoscopic examination
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Monitor for delayed wound healing, especially after surgery
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Watch for secondary infections – bacterial, fungal, or viral
Caution In
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Glaucoma or family history of glaucoma
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Cataract patients (risk of posterior subcapsular cataract)
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Diabetics (risk of increased IOP)
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Contact lens wearers – risk of corneal ulceration or toxicity with preservatives
Adverse Effects
Local (Ocular)
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Increased IOP, optic nerve damage
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Posterior subcapsular cataract (with chronic use)
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Delayed corneal healing
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Secondary ocular infection, including masked bacterial or fungal infections
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Corneal thinning or perforation in prolonged use
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Transient burning or stinging on application
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Blurred vision, especially with suspensions
Systemic
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Minimal systemic absorption with proper use
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Rare systemic corticosteroid effects with long-term high-frequency dosing
Drug Interactions
Although systemic absorption is minimal, certain precautions apply:
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Ocular NSAIDs: May increase risk of corneal thinning or ulceration
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Ocular antihypertensives: Monitor IOP closely
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Antibiotics: Combined formulations (e.g., Tobradex) reduce infection masking risk
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Vaccines: Avoid live vaccines concurrently if systemic absorption occurs in significant quantities
Comparison with Other Ophthalmic Corticosteroids (No Tables)
Dexamethasone vs. Prednisolone Acetate
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Both are high-potency steroids for anterior inflammation
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Prednisolone acetate may penetrate aqueous humor more effectively
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Dexamethasone has a longer half-life and is more lipophilic
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Both can elevate IOP, though dexamethasone may do so more potently
Dexamethasone vs. Fluorometholone
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Fluorometholone is considered a "soft" steroid with less IOP elevation
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Preferred in long-term use or post-surgical prophylaxis
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Dexamethasone is more effective in moderate to severe inflammation
Dexamethasone vs. Loteprednol
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Loteprednol is an ester-based corticosteroid, rapidly deactivated
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Lower risk of IOP rise than dexamethasone
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Loteprednol preferred for chronic use (e.g., allergic conjunctivitis)
Patient Counseling Points
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Shake bottle before use (if suspension)
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Use drops exactly as prescribed—do not exceed duration
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Wash hands before and after application
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Avoid touching the dropper tip to the eye or any surface
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Wait 5 minutes between multiple eye medications
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Do not wear contact lenses during treatment (and 15 minutes after application)
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Store in a cool, dry place. Some formulations require refrigeration
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Report vision changes, eye pain, or persistent redness immediately
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Attend all follow-up eye pressure checks if using longer than 1 week
Use in Special Populations
Pregnancy
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Use only if benefits outweigh risks
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Risk of fetal effects minimal with short-term local ocular use
Lactation
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Limited systemic absorption—generally considered compatible with breastfeeding
Pediatrics
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Use with strict supervision; higher risk of systemic absorption and ocular side effects
Geriatrics
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Close monitoring for IOP elevation, cataract development, and secondary infection
Withdrawal and Tapering
Tapering is essential if used for >1 week to avoid rebound ocular inflammation. Do not stop suddenly—reduce dose gradually based on ophthalmologist’s guidance
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