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Near real-time adverse drug reaction surveillance within population-based health networks: methodology considerations for data accrual†

  1. Taliser R. Avery1,2,*,
  2. Martin Kulldorff1,2,
  3. Yury Vilk1,
  4. Lingling Li1,
  5. T. Craig Cheetham2,3,
  6. Sascha Dublin2,4,
  7. Robert L. Davis2,6,
  8. Liyan Liu2,5,
  9. Lisa Herrinton2,5,
  10. Jeffrey S. Brown1,2

Article first published online: 12 FEB 2013

DOI: 10.1002/pds.3412

Issue

Pharmacoepidemiology and Drug Safety

Pharmacoepidemiology and Drug Safety

Volume 22, Issue 5, pages 488–495, May 2013

Additional Information

How to Cite

Avery, T. R., Kulldorff, M., Vilk, Y., Li, L., Craig Cheetham, T., Dublin, S., Davis, R. L., Liu, L., Herrinton, L. and Brown, J. S. (2013), Near real-time adverse drug reaction surveillance within population-based health networks: methodology considerations for data accrual. Pharmacoepidem. Drug Safe., 22: 488–495. doi: 10.1002/pds.3412

Author Information

  1. 1

    Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, Boston, MA, USA

  2. 2

    The HMO Research Network Center for Education and Research in Therapeutics, Boston, MA, USA

  3. 3

    Pharmacy Analytical Service, Kaiser Permanente, Downey, CA, USA

  4. 4

    Group Health Research Institute, Seattle, WA, USA

  5. 5

    Division of Research, Kaiser Permanente Northern California, Oakland, CA, USA

  6. 6

    Center for Health Research, Kaiser Permanente Georgia, Atlanta, GA, USA

*Correspondence to: T. R. Avery, Department of Population Medicine, Harvard Medical School and HPHC Institute, 133 Brookline Avenue, 6th Floor, Boston, MA 02215, USA. E-mail: Taliser_Avery@hphc.org

  1. †

    Prior presentation: These data have not previously been presented.

Publication History

  1. Issue published online: 3 MAY 2013
  2. Article first published online: 12 FEB 2013
  3. Manuscript Accepted: 2 JAN 2013
  4. Manuscript Revised: 28 NOV 2012
  5. Manuscript Received: 29 AUG 2012

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