GNH USA

Europe — EMA

Iluvien

GNH USA supplies Iluvien (Fluocinolone Acetonide), a corticosteroid for diabetic macular edema and chronic non‑infectious posterior uveitis.

Fluocinolone Acetonide

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What is Fluocinolone Acetonide?

Fluocinolone Acetonide, the active ingredient in Iluvien, is a corticosteroid presented as a 0.19 mg intravitreal sustained‑release implant for intravitreal use. It treats diabetic macular edema and chronic non‑infectious posterior uveitis in adult patients.

GNH USA supplies Iluvien as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

What is Fluocinolone Acetonide used for?

Iluvien is indicated for ocular conditions characterized by inflammation and fluid accumulation.

Diabetic macular edema: reduces retinal thickness and improves visual acuity. Chronic non‑infectious posterior uveitis: controls intra‑ocular inflammation and helps preserve vision.

What are the side effects of Fluocinolone Acetonide?

Iluvien may cause ocular and systemic adverse reactions, which vary in frequency and severity.

Common Side Effects: - Elevated intraocular pressure - Cataract formation or progression - Vitreous floaters - Mild ocular discomfort or irritation - Conjunctival hyperemia - Transient blurred vision

Serious or Rare Side Effects: - Persistent or uncontrolled intraocular pressure leading to glaucoma - Endophthalmitis or intraocular infection - Retinal detachment or tear - Severe cataract requiring surgery - Vitreous hemorrhage

What precautions apply to Fluocinolone Acetonide?

Prior to Iluvien implantation, clinicians should assess ocular health and consider patient history.

Monitor intraocular pressure: schedule regular pressure checks post‑implant. Assess cataract status: evaluate lens opacity before and after treatment. Avoid in active ocular infection: postpone implantation until infection resolves. Use with caution in patients with glaucoma or a history of steroid‑responsive pressure rise. Do not combine with other intraocular corticosteroid implants. Store at ambient temperature: keep in original packaging, protect from moisture and direct sunlight.

What does Fluocinolone Acetonide interact with?

Iluvien may interact with other ocular or systemic agents that affect intraocular pressure or inflammation.

Major Interactions (Avoid): - Concurrent use of other intravitreal corticosteroid implants: risk of additive pressure elevation. - Systemic potent CYP3A4 inducers (e.g., rifampin) that could alter steroid metabolism.

Moderate Interactions (Monitor Closely): - Topical ocular steroids: monitor intraocular pressure closely. - Antiglaucoma medications: adjust dosing if intraocular pressure rises. - Anticoagulants: watch for increased risk of intraocular hemorrhage during implantation.

Frequently asked questions

What conditions is Iluvien used to treat?+
Iluvien is approved for the treatment of diabetic macular edema and chronic non‑infectious posterior uveitis. In both conditions, the implant delivers a low‑dose corticosteroid directly to the eye to reduce fluid accumulation, inflammation, and to help preserve or improve visual acuity.
How does fluocinolone acetonide work in Iluvien?+
Fluocinolone acetonide activates glucocorticoid receptors in ocular tissues, suppressing inflammatory cytokines and reducing vascular leakage. The sustained‑release implant provides a continuous, low‑level exposure within the vitreous cavity, maintaining anti‑inflammatory activity while limiting systemic exposure.
What is the usual dose of Iluvien?+
Iluvien is supplied as a single‑use 0.19 mg intravitreal implant. The exact dosing schedule, including whether a repeat implantation is needed, is determined by the prescribing ophthalmologist based on the patient’s clinical response and disease progression.
Is Iluvien safe to use during pregnancy or breastfeeding?+
The safety of Iluvien in pregnancy and lactation has not been established. Because the implant delivers a corticosteroid directly to the eye, clinicians should weigh potential risks and benefits and consider alternative therapies when treating pregnant or nursing patients.
How do I order Iluvien from GNH USA?+
To request Iluvien, submit an enquiry on the product page at gnh-usa.com with the required quantity. GNH USA works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements) and the necessary import documentation.
How does Iluvien compare with other ocular corticosteroid treatments?+
Iluvien provides a sustained‑release delivery of fluocinolone acetonide for up to 36 months, reducing the need for frequent injections. Compared with short‑acting intravitreal steroids such as triamcinolone or dexamethasone implants, Iluvien offers longer durability but may carry a higher cumulative risk of intraocular pressure rise and cataract formation.
What are the storage requirements for Iluvien?+
Store Iluvien at ambient temperature, below 25 °C. Keep the implant in its original sealed container, protect it from moisture and direct sunlight, and avoid exposing it to extreme temperatures or mechanical shock.
How is Iluvien administered?+
Iluvien is implanted into the vitreous cavity of the eye by a qualified ophthalmic surgeon using a specialized applicator. The procedure is performed under sterile conditions, typically in an operating room or a designated procedure suite, and does not require systemic administration.
What are the most serious risks associated with Iluvien?+
The most serious risks include sustained elevation of intraocular pressure that may lead to glaucoma, development or progression of cataracts requiring surgery, and rare but severe complications such as endophthalmitis, retinal detachment, or vitreous hemorrhage. Patients should be monitored regularly for these events.
Who should not use Iluvien?+
Iluvien is contraindicated in patients with active ocular infection, uncontrolled glaucoma, or a known hypersensitivity to fluocinolone acetonide or any component of the implant. It should also be avoided in individuals who have received another intravitreal corticosteroid implant within the same eye.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Fluocinolone Acetonide
Route
Intravitreal Use
Manufacturer
Alimera Sciences Europe Limited
Origin
EU

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