The overall incidence of treatment-related adverse events was reduced significantly in the bimatoprost 0.01 and bimatoprost 0.0125 groups compared with the bimatoprost 0.03 group (P or.034). The percentage of patients with a moderate to severe increase from the baseline macroscopic hyperemia score was: bimatoprost 0.01.
In addition, because these products may exacerbate inflammation, caution should be used in patients with active intraocular inflammation (e.g., uveitis ). Macular Edema Macular edema, including cystoid macular edema, has been reported during treatment with bimatoprost ophthalmic solution.
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In less than 1 of patients, intraocular inflammation was reported as iritis. Systemic adverse events reported in approximately 10 of patients were infections (primarily colds and upper respiratory tract infections). The following systemic adverse events reported in approximately 1 to 5 of patients, in descending.SIDE.
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Tell your doctor right away if any of these unlikely but serious side effects occur: eye pain, suspected eye infection (discharge, unusual redness, swelling of eyes rapid vision changes (such as loss of vision ).Call your healthcare provider if you develop open sores or drainage.
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