Dexamethasone Intravitreal Implant 0.7 mg
Brand names: Ozurdex
The dexamethasone intravitreal implant is a sustained-release corticosteroid device injected into the vitreous to treat conditions such as macular oedema secondary to retinal vein occlusion, diabetic macular oedema and non-infectious posterior uveitis.
ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.
Clinical monograph
How it works
The biodegradable implant gradually releases dexamethasone within the eye, suppressing inflammation and reducing vascular permeability to lessen retinal oedema.
Prescribing in practice
- It must be administered by an appropriately trained ophthalmologist under aseptic conditions, with patients warned to report symptoms of endophthalmitis or retinal detachment without delay.
- It commonly raises intraocular pressure and accelerates cataract formation, and is contraindicated in active or suspected ocular or periocular infection and in advanced glaucoma.
- Caution is required in eyes with a compromised posterior lens capsule, as the implant may migrate into the anterior chamber.
Monitoring
Monitor intraocular pressure and assess for infection, raised pressure and lens changes following injection.
Counselling the patient
- Seek urgent ophthalmic care if you develop eye pain, increasing redness, reduced vision or increased sensitivity to light.
- Floaters may increase temporarily after the injection.
- Attend all scheduled reviews so your eye pressure and retina can be checked.
Evidence & guidelines
Use in retinal vein occlusion-related and diabetic macular oedema and non-infectious uveitis is supported by NICE technology appraisals and randomised trial evidence.
Reference: NICE TA229; NICE TA349; NICE TA409; MACULAR Trial; SPC Ozurdex; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Acute Red Eye / Vision Loss Screen · RCOphth 2020; NICE CKS
- Idiopathic Intracranial Hypertension · ABN; consensus 2018
- Acute Red Eye Assessment · RCOphth / AAO
- Acute Angle Closure Glaucoma · RCOphth / EGS Guidelines
- Retinal Detachment · RCOphth Guidelines / EURETINA
- Diabetic Retinopathy — Screening and Management · NICE NG28 2016 / NHS DES Programme