Latisse (bimatoprost) Detailed View: Safety Labeling Changes Approved By FDA Center for Drug Evaluation and Research (CDER ) September 2014. Summary View.Valuable resources for patients who use LUMIGAN (bimatoprost ophthalmic solution) 0.01 for glaucoma or high eye pressure.
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RETURN TO RESOURCES LEARN MORE 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.
You are at the highest risk if these problems are pre-existing before injection. Swallowing problems may last for several months. Spread of toxin effects. The effect of botulinum toxin may affect areas away from the injection site and cause serious symptoms including: loss of strength.- How to use Careprost? - When to apply? - For how long should it be applied? - What if you take too much (overdose)? - What if you miss the dose? LATISSE under doctor care. May cause brown darkening of the colored part of the eye which is likely permanent. LATISSE may cause eyelid skin darkening which may be reversible. Only apply at base of upper lashes.
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.Important Safety Information 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.
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.Do not take BOTOX Cosmetic if you: are allergic to any of the ingredients in BOTOX Cosmetic (see Medication Guide for ingredients had an allergic reaction to any other botulinum toxin product such as Myobloc (rimabotulinumtoxinB Dysport (abobotulinumtoxinA or Xeomin (incobotulinumtoxinA have a skin infection.
The safety for use in patients with excessive scarring or pigmentation disorders has not been studied and may result in additional scars or pigmentation changes. Unintentional injection into a blood vessel can occur and, while rare, could result in serious complications which may be permanent.Serious and/or immediate allergic reactions have been reported. They include: itching, rash, red itchy welts, wheezing, asthma symptoms, or dizziness or feeling faint. Get medical help right away if you are wheezing or have asthma symptoms, or if you become dizzy or faint.