bimatoprost ophthalmic implant (Durysta)

Brand Names: Durysta

Generic Name: bimatoprost ophthalmic implant

What is bimatoprost ophthalmic implant (Durysta) (Durysta)?

Bimatoprost ophthalmic (for the eyes) lowers pressure in the eye by increasing the amount of fluid that drains from the eye.

Bimatoprost ophthalmic implant (Durysta) is used to treat adults with open-angle glaucoma and other causes of high pressure inside the eye.

Bimatoprost ophthalmic implant may also be used for purposes not listed in this medication guide.

What are the possible side effects of Durysta (Durysta)?

Get emergency medical help if you have signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have:

  • worsening eye pain or redness;
  • vision changes;
  • increased sensitivity to light; or
  • signs of eye infection--puffy eyelids, eye redness, severe discomfort, crusting or drainage, vision loss.

Common side effects may include:

  • eye redness or a blood spot on the white of your eye;
  • eye pain;
  • feeling like something is in your eye;
  • eye dryness or irritation;
  • blurred vision, inflammation of the iris;
  • headache;
  • increased pressure inside the eye; or
  • a loss of cells on the inner layer of your cornea.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What is the most important information I should know about Durysta (Durysta)?

You should not be treated with Durysta if you have an eye infection, problems with your cornea, if you have had a corneal transplant, or if the sack around the lens of your eye is missing or torn.

What should I discuss with my healthcare provider before receiving (Durysta) (Durysta)?

You should not be treated with Durysta if you are allergic to bimatoprost, or if you have:

  • an infection in or around your eye;
  • problems with your cornea (the surface of your eye);
  • a history of corneal transplant; or
  • if the sack around the lens of your eye (posterior lens capsule) is missing or torn.

Tell your doctor if you have ever had:

  • eye problems in the space where your cornea meets your iris (the colored part of your eye);
  • cataract surgery; or
  • inflammation inside your eye.

Durysta may cause a gradual change in the color of brown eyes, usually an increase in pigment. This change occurs slowly and may be permanent even after your treatment ends.

How is Durysta given (Durysta)?

Durysta is a tiny implant that is placed directly inside your eye (usually one per eye) by your eye doctor.

Your doctor may use a medicine to numb your eye before inserting the implant.

The Durysta implant will dissolve over time, and its effects should last for several months.


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What happens if I miss a dose (Durysta)?

Durysta is used as a single implant and does not have a daily dosing schedule.

What happens if I overdose (Durysta)?

Since this medicine is given by a healthcare professional in a medical setting, an overdose is unlikely to occur.

What should I avoid after receiving Durysta (Durysta)?

Follow your doctor's instructions about any restrictions on food, beverages, or activity.

What other drugs will affect Durysta (Durysta)?

Medicine used in the eyes is not likely to be affected by other drugs you use. But many drugs can interact with each other. Tell each of your healthcare providers about all medicines you use, including prescription and over-the-counter medicines, vitamins, and herbal products.

Where can I get more information (Durysta)?

Your pharmacist can provide more information about bimatoprost ophthalmic implant (Durysta).

Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.
Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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Reviewed on 10/12/2022

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