"The U.S. Food and Drug Administration today approved the Argus II Retinal Prosthesis System, the first implanted device to treat adult patients with advanced retinitis pigmentosa (RP). The device, which includes a small video camera, transmitter "...
ACULAR® solution is contraindicated in patients with previously demonstrated hypersensitivity to any of the ingredients in the formulation.
Last reviewed on RxList: 6/29/2012
This monograph has been modified to include the generic and brand name in many instances.
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