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Appendix: Additional Drug Repositioning Resources and Links

  • Mitchell M
  • Barratt M
Wiley, (2012), 457-468
DOI: 10.1002/9781118274408.app1
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Abstract

The Adverse Event Reporting System (AERS) is a computerized information database designed to support the FDA's post-marketing safety surveillance program for all approved drug and therapeutic biologic products. Submissions to the database are voluntary as they ...

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Mitchell, M. A., & Barratt, M. J. (2012). Appendix: Additional Drug Repositioning Resources and Links. In Drug Repositioning (pp. 457–468). Wiley. https://doi.org/10.1002/9781118274408.app1

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