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(Reuters) -The U.S. Food and Drug Administration had approved Eyenovia's eye drops to reduce inflammation and pain in patients who have undergone eye surgery, Taiwan-based Formosa...
Update (February 3, 2024): It looks like we're starting off the year right where we left off, when it comes to eye drop recalls. This time, it's a warning, not an official product recall, being ...
The FDA tested the products and found that they had been contaminated with microbes and were not sterile. “Under the Federal Food, Drug and Cosmetic Act, eye drops must be sterile to be safe for...
On March 1, Apotex recalled prescription eye drops, and on March 3, Pharmedica recalled eye drops that treat eye irritation. P. aeruginosa has not been associated in either of these products. Signs and symptoms. Symptoms may include discharge from the eyes, pain or redness in the eyes, blurry vision, and increased sensitivity to light.
Medication is used for strabismus in certain circumstances. In 1989, the US FDA approved botulinum toxin therapy for strabismus in people over 12 years old. Most commonly used in adults, the technique is also used for treating children, in particular children affected by infantile esotropia.
In the United States, in December 2017, the Food and Drug Administration (FDA) approved a 0.02% ophthalmic solution for the lowering of elevated intraocular pressure in people with open-angle glaucoma or ocular hypertension. The European Medicines Agency approved it in 2019 for the same uses under the brand name Rhokiinsa.
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