Any adverse event, whether mild, severe or serious, that is related to the OriLens, should be treated immediately and reported to OptoLight.
Please send to us a written report elaborating all of the measures that were taken by the surgeon.
Please report a mild (easily treated) or moderate (discomfort) adverse event within 5 working days.
Severe adverse events should be reported immediately.
The report should include an evaluation by the surgeon whether the adverse event is related to the OriLens. This estimation should be classified as one of three options: probable related, remotely related or unrelated to the OriLens Implantation.