Stopped: Business decision to stop the program.
This observational study will evaluate the safety, efficacy, characteristics of patients, characteristics of physicians and quality of life in patients who are prescribed OZURDEX® as treatment for non-infectious uveitis of the posterior segment of the eye in France.
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Percentage of Participants with Best Corrected Visual Acuity (BCVA) ≥15 Letters
Timeframe: 2 Months