"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 "...
Contraindicated in those persons who have shown hypersensitivity to any component of this preparation. Do not use via the intrathecal or arterial routes. Use of this product is generally inadvisable if the patient has history of severe allergy to products containing fluorescein.This monograph has been modified to include the generic and brand name in many instances.
Last reviewed on RxList: 9/23/2008
Additional Ak-Fluor Information
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