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Description
Early intervention is critical in managing NAION and potentially preserving remaining vision
AOD 9604 demonstrated virtually no significant adverse effects across all human trials at doses up to 1mg per day
Intensified monitoring with detailed ultrasonography
The presentation of NAION is classically described as acute painless visual loss, often noted upon awakening, accompanied by an altitudinal visual field defect and dyschromatopsia
Relative reductions in LFC at week 24 measured 14.0%, 56.3%, 75.2%, and 76.4%
