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Guest Editorial

medWatch: FDA'S Medical Products Reporting Program

A joint effort toward improved public health

, MD & , MPH, RPh
Pages 13-16 | Published online: 30 Jun 2015

References

  • Griffin GC, Parkinson RW, Woolley BH. Report every adverse drug reaction! We're all in this together. Postgrad Med 1997; 101(4):13–6
  • National Childhood Vaccine Injury Act of 1986. Public Health Service Act §2125, 42USC §300aa-25 (Suppl 1987)
  • Joint Commission on Accreditation of Healthcare Organizations. 1996 Comprehensive accreditation manual for hospitals. Oakbrook Terrace, I11: The Joint Commission, 1995
  • Medical device user facility and manufacturer reporting, certification and registration; delegations of authority; medical device reporting procedures. Federal Register 63577–63606 (1995)
  • White GG, Weick-Brady MD. Improving patient care by reporting problems with medical devices. MedWatch continuing education article. Available at: http://www.fda.gov/medwatch/articles.htm. Accessed 1998 Jan 29
  • Kennedy DL, Goldman SA. Monitoring for adverse drug events. (Editorial) Am Fam Physician 1997; 56(7):1718–21
  • Goldman SA. The clinical impact of adverse event reporting. MEDwatch continuing education article. Available at: http://www.fda.gov/medwatch/articles.htm. Accessed 1998 Jan 29
  • Finney DJ. The detection of adverse reactions to therapeutic drugs. Stat Med 1982; 1(2):153–61
  • Rossi AC, Knapp DE. Discovery of new adverse drug reactions: a review of the Food and Drug Administration's spontaneous reporting system. JAMA 1984; 252(8):1030–33
  • Goldman SA, Kennedy DL, Lieberman R, eds. Clinical therapeutics and the recognition of drug-induced disease. Medwatch continuing education article. Available at: http://www.fda.gov/medwatch/articles.htm. Accessed 1998 Feb 4

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