During treatment with LUMIGAN® 0.01% you may experience:
In a 12-month clinical study with LUMIGAN® 0.01%, the most common adverse reaction was eye redness (31%). Approximately 1.6% of patients stopped therapy due to eye redness with LUMIGAN® 0.01%.
Talk to your doctor if you experience any side effects.
Indication
LUMIGAN® (bimatoprost ophthalmic solution) 0.01% is used for the reduction of high
eye pressure, also called intraocular pressure (IOP), in people with open-angle
glaucoma or ocular hypertension.
Important Safety Information
Do not use LUMIGAN® 0.01% if you are allergic to any of the ingredients.
LUMIGAN® (bimatoprost ophthalmic solution) 0.01% can cause increased brown coloring
of the iris, which may be permanent. LUMIGAN® 0.01% can cause darkening of the eyelid
skin and eyelashes, which may be reversible after treatment is stopped. The long-term
effects of increased dark coloring are not known.
LUMIGAN® 0.01% may slowly increase the growth and thickness of eyelashes, which are usually reversible after treatment is stopped.
Indication
LUMIGAN® (bimatoprost ophthalmic solution) 0.01% is used for the
reduction of high eye pressure, also called intraocular pressure (IOP), in people
with open-angle glaucoma or ocular hypertension.
Important Safety Information
Do not use LUMIGAN® 0.01% if you are allergic to any of the ingredients.
LUMIGAN® (bimatoprost ophthalmic solution) 0.01% can cause increased
brown coloring of the iris, which may be permanent. LUMIGAN® 0.01%
can cause darkening of the eyelid skin and eyelashes, which may be reversible after
treatment is stopped. The long-term effects of increased dark coloring are not known.
LUMIGAN® 0.01% may slowly increase the growth and thickness of eyelashes, which are usually reversible after treatment is stopped.
Prostaglandin analogs, including bimatoprost, have been reported to cause inflammation inside the eye. Also, treatment with LUMIGAN® 0.01% may make existing inflammation worse.
Macular edema (swelling of the macula), including cystoid macular edema, has been reported during treatment with bimatoprost ophthalmic solution. LUMIGAN® 0.01% should be used with caution in patients without a natural lens, in patients with a torn posterior lens capsule who have an artificial lens implant, or in patients with known risk factors for macular edema.
Avoid allowing the tip of the dispensing bottle to touch the eye, anything around the eye, fingers, or any other surface to avoid contamination by common bacteria known to cause eye infections. Using contaminated solutions can cause serious damage to the eye and loss of vision.
If you have eye surgery, eye trauma or infection, or develop any eye reactions, immediately consult with your physician about continuing the use of LUMIGAN® 0.01%.
LUMIGAN® 0.01% contains an ingredient that may be absorbed by and cause discoloration of soft contact lenses. If you wear contact lenses, remove them before using LUMIGAN® 0.01%. Then wait 15 minutes after using LUMIGAN® 0.01% before you put your contacts back into your eyes.
The most common side effect is eye redness. Other side effects include growth of eyelashes and itchy eyes.
