Perfluorohexyloctane ophthalmic, marketed under the brand name Miebo, is an FDA-approved medication for treating dry eye disease. The approval was granted to this innovative treatment on May 18, 2023, providing a new option for individuals suffering from the discomfort and vision issues associated with dry eye disease.
Perfluorohexyloctane ophthalmic solution is classified under the drug class of ophthalmic anti-inflammatory agents. It is specifically designed to treat symptoms of dry eye disease by lubricating the eyes, reducing dryness, and alleviating associated discomfort.
Common side effects of perfluorohexyloctane ophthalmic may include blurred vision. Serious allergic reactions such as hives, difficulty breathing, and swelling of the face, lips, tongue, or throat require immediate medical attention.
While it is unlikely that eye medications will be affected by other drugs, always inform your healthcare provider about all medicines you use, including prescription and over-the-counter drugs, vitamins, and herbal products.
Perfluorohexyloctane ophthalmic (Miebo) is an FDA-approved medication for the treatment of dry eye disease. Approved on May 18, 2023, this solution offers relief from the symptoms of dry eye, such as dryness and discomfort, and provides a new option for those seeking effective treatment. Always use the medication as directed by your healthcare provider and be aware of potential side effects and interactions.
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