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Comparative Safety and Tolerability of Anti-VEGF Therapy in Age-Related Macular Degeneration

Journal

DRUG SAFETY
Volume 38, Issue 3, Pages 279-293

Publisher

ADIS INT LTD
DOI: 10.1007/s40264-015-0273-0

Keywords

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Funding

  1. National Institutes of Health/National Eye Institute [NIH/NEI K23-EY022947-01A1]
  2. Ohio Department of Development Grant [TECH-13-059]
  3. Research to Prevent Blindness
  4. NATIONAL EYE INSTITUTE [K23EY022947] Funding Source: NIH RePORTER

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Neovascular age-related macular degeneration (NVAMD) is one of the leading causes of blindness. Over the last decade, the treatment of NVAMD has been revolutionized by the development of intravitreal anti-vascular endothelial growth factor (VEGF) therapies. Several anti-VEGF medications are used for the treatment of NVAMD. The safety and tolerability of these medications deserve review given the high prevalence of NVAMD and the significant utilization of these medications. Numerous large randomized clinical trials have not shown any definitive differential safety relative to ocular or systemic safety of these medications. Intravitreal anti-VEGF therapy does appear to impact systemic VEGF levels, but the implications of these changes remain unclear. One unique safety concern relates drug compounding and the potential risks of contamination, specifically for bevacizumab. Continued surveillance for systemic safety concerns, particularly for rare events, is merited. Overall, these medications are well tolerated and effective in the treatment of NVAMD.

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