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Brilliant Blue G
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Brilliant Blue G Side Effects

brilliant blue g vial and package
The U.S. Food and Drug Administration (FDA) has received reports of fungal endophthalmitis in patients who were given Brilliant Blue G (BBG) during eye surgeries. Clinicians in several states reported the adverse events. The FDA, along with the U.S. Centers for Disease Control and Prevention (CDC) and local and state public health agencies, are actively investigating these adverse events. The BBG was supplied by Franck's Compounding Lab, Ocala, Florida. Franck's Pharmacy issued a recall on March 9, 2012, of all lots of Brilliant Blue G and issued a recall letter. Brilliant Blue G is not an approved drug in the U.S.