Imagine
What You’ll See?

Your vision is so important. Seeing is the number-one way to experience many magical moments in life. But if you have DME, your vision may be affected.

See how ILUVIEN^®(fluocinolone acetonide intravitreal implant) 0.19 mg could help.

Take a journey with us

See what to expect

View patient experiences

See more stories

Wondering how to talk to your eye doctor about ILUVIEN?

Ask the right questions

Fewer injections could help you embrace life’s magical moments

Learn about ways to help pay for treatment with ILUVIEN

Financial Assistance
Services

ILUVIEN Patient
Assistance Program

Independent Financial
Assistance Foundations

ILUVIEN CoPay
Program

Find out more

Important Safety Information

Indication

ILUVIEN^® (fluocinolone acetonide intravitreal implant) 0.19 mg is indicated for the treatment of diabetic macular edema (DME) in patients who have been previously treated with a course of corticosteroids and did not have a clinically significant rise in intraocular pressure.

Important Safety Information

Do not use ILUVIEN if you have or think you might have an infection in or around the eye.
ILUVIEN should not be used if you have advanced glaucoma.
You should not use ILUVIEN if you are allergic to any ingredients of ILUVIEN.
Injections into the vitreous in the eye are associated with a serious eye infection
(endophthalmitis), eye inflammation, increased eye pressure, glaucoma, and retinal detachments. Your
eye doctor should monitor you regularly after the injection.
Use of corticosteroids including ILUVIEN may produce cataracts (ILUVIEN 82%; sham 50%), increased
eye pressure (ILUVIEN 34%; sham 10%), glaucoma, and may increase secondary eye infections due to
bacteria, fungi, or viruses. Let your doctor know if you have a history of herpes viral infections of
the eye.
If the posterior capsule of the lens of your eye is missing or torn the ILUVIEN implant may move to
the front chamber of the eye.
The most common side effects reported in patients with diabetic macular edema who were treated with
ILUVIEN include cataracts (ILUVIEN 82%; sham 50%) and increased eye pressure (ILUVIEN 34%; sham 10%).

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit
www.fda.gov/medwatch, or call 1-800-FDA-1088.

One Injection

Imagine What You’ll See?

Take a journey with us

View patient experiences

Wondering how to talk to your eye doctor about ILUVIEN?

Learn about ways to help pay for treatment with ILUVIEN

Financial Assistance Services

ILUVIEN Patient Assistance Program

Independent Financial Assistance Foundations

ILUVIEN CoPay Program

Indication

Important Safety Information

Imagine
What You’ll See?

Financial Assistance
Services

ILUVIEN Patient
Assistance Program

Independent Financial
Assistance Foundations

ILUVIEN CoPay
Program