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Decadron Ocumeter Side Effects

Generic name: dexamethasone ophthalmic

Medically reviewed by Drugs.com. Last updated on Jun 1, 2024.

Note: This document provides detailed information about Decadron Ocumeter.

For healthcare professionals

Applies to dexamethasone ophthalmic: intraocular implant, intraocular suspension, ophthalmic insert, ophthalmic ointment, ophthalmic solution, ophthalmic suspension Side Effects associated with dexamethasone ophthalmic. Some dosage forms listed on this page may not apply specifically to the brand name Decadron Ocumeter.

For healthcare professionals

Applies to dexamethasone ophthalmic: intraocular implant, intraocular suspension, ophthalmic insert, ophthalmic ointment, ophthalmic solution, ophthalmic suspension.

General adverse events

The most commonly reported side effects were cataract, elevation of intraocular pressure, and conjunctival hemorrhage.[Ref]

Ocular

Postmarketing experience: Complication of device insertion (implant misplacement), device dislocation with or without corneal edema, endophthalmitis, hypotony of the eye (associated with vitreous leakage due to injection), retinal detachment[Ref]

Cardiovascular

Nervous system

Respiratory

Endocrine

Cushing's syndrome and adrenal suppression may occur at doses higher than recommended in predisposed patients including children and those on CYP P450 3A4 inhibitors.

References

1. (2001) "Product Information. Decadron Ocumeter (dexamethasone ophthalmic)." Merck & Co., Inc

2. Cerner Multum, Inc. "UK Summary of Product Characteristics."

3. Cerner Multum, Inc. "Australian Product Information."

4. (2009) "Product Information. Ozurdex (dexamethasone ophthalmic)." Allergan Inc

Further information

Decadron Ocumeter side effects can vary depending on the individual. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Note: Medication side effects may be underreported. If you are experiencing side effects that are not listed, submit a report to the FDA by following this guide.