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We read with interest the article by Fung et al1 assessing complications related to single or repeat intravitreal injections of bevacizumab. We congratulate the authors on studying this innovative treatment via the internet and greatly appreciate the effort to gather timely information about the potentially related adverse events. When using a product for an indication not in the approved label, doctors have the responsibility to be well informed about the product and its potential risks, and to base its use on firm scientific rationale and sound medical evidence.2 Informed consent must also depend on a full discussion of all potential complications of the treatment proposed. Unfortunately, some pitfalls of this survey have restricted the explanatory power of the presented results.3
The definition of the study population remains …
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