May 2008
Volume 49, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2008
Incidence of Adverse Events Associated With the Use of Intravitreal Bevacizumab (Avastin®) in Eyes With Exudative Age Related Macular Degeneration
Author Affiliations & Notes
  • V. R. Romeiro
    Romeiro Clinica de Olhos, Pouso Alegre, Brazil
  • B. R. A. Nassaralla
    Cataract and Cornea, Instituto de Olhos de Goiania, Goiania, Brazil
  • J. J. Nassaralla, Jr.
    Retina and Vitreous, Instituto de Olhos deGoiania, Goiania, Brazil
  • Footnotes
    Commercial Relationships  V.R. Romeiro, None; B.R.A. Nassaralla, None; J.J. Nassaralla, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science May 2008, Vol.49, 5561. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      V. R. Romeiro, B. R. A. Nassaralla, J. J. Nassaralla, Jr.; Incidence of Adverse Events Associated With the Use of Intravitreal Bevacizumab (Avastin®) in Eyes With Exudative Age Related Macular Degeneration. Invest. Ophthalmol. Vis. Sci. 2008;49(13):5561.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

Purpose: : To identify adverse events associated with the use of intravitreal Avastin ® (Roche, Rio de Janeiro, Brazil) in patients with exudative Age-Related Macular Degeneration (AMD).

Methods: : Retrospective review of a consecutive series of 500 eyes of 332 patients who received two intravitreal Avastin to treat exudative AMD. All patients had at least three month of follow up. We performed a chart review of these patients to evaluate the incidence of adverse events in the second and third month after the initial injection. Standard ocular and systemic adverse events, routinely utilized in clinical trials, were evaluated. The ocular adverse events included accelerated formation of cataract, ocular hypertension (>30mm) for more than one week, clinically significant inflammation, significant retinal or choroidal vascular abnormalities not seen at baseline, and adverse events associated with the injection procedure (conjunctival injection, conjunctival hemorrhage, pain, soreness, irritation, vitreous hemorrhage, traumatic cataract, retinal detachment, endophthalmitis). We also looked for systemic adverse events, including any unfavorable or unintended sign, symptom, or disease temporally associated with the use of Avastin, whether or not considered related to the medicinal product.

Results: : Of the 500 eyes injected, eight eyes had significant inflammation (1+ cell and flare), three eye had significant punctate keratitis, one eye had vitreous hemorrhage, two eyes accelerated formation of cataract, 376 eyes conjunctival hemorrhage, one eye endophthalmitis and seven eyes developed pain during the follow up period.

Conclusions: : Avastin was well tolerated and had a low rate of ocular adverse events in this study.

Clinical Trial: : www.clinicaltrials.gov NCT00556348

Keywords: age-related macular degeneration • retinal neovascularization • retina 
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×