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題名：藥物不良反應防護機制的建構與成效
書刊名：臺灣臨床藥學雜誌
作者：林子鈺／鄭吉元／陳琦華
作者(外文)：Lin, Tzu-yu／Cheng, Chi-yuan／Chen, Chi-hua
出版日期：2018
卷期：26:2
頁次：頁150-157
主題關鍵詞：藥物不良反應；資訊系統；系統架構；Adverse drug reaction；Information technology；Systems approach
原始連結：連回原系統網址new window
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期刊論文
1.Lesar, T. S.、Briceland, L.、Stein, D. S.(1997)。Factors related to errors in medication prescribing。JAMA: the Journal of the American Medical Association，277(4)，312-317。  new window
2.Nebeker, J. R.、Barach, P.、Samore, M. H.(2004)。Clarifying adverse drug events: A clinician's guide to terminology, documentation, and reporting。Annals of Internal Medicine，140(10)，795-801。  new window
3.Morimoto, T.、Gandhi, T. K.、Seger, A. C.、Hsieh, T. C.、Bates, D. W.(2004)。Adverse drug events and medication errors: detection and classification methods。Qual Saf Health Care，13，306-314。  new window
4.Bates, D. W.、Spell, N.、Cullen, D. J.、Burdick, E.、Laird, N.、Petersen, L. A.、Small, S. D.、Sweitzer, B. J.、Leape, L. L.(1997)。The costs of adverse drug events in hospitalized patients. Adverse Drug Events Prevention Study Group。JAMA，277(4)，307-311。  new window
5.Aronson, J. K.(2009)。Medication errors: definitions and classification。Br J Clin Pharmacol，67，599-604。  new window
6.Gandhi, T. K.、Seger, D. L.、Bates, D. W.(2000)。Identifying drug safety issues: from research to practice。Int J Qual Health Care，12，69-76。  new window
7.Lisby, M.、Nielsen, L. P.、Brock, B.(2010)。How are medication errors defined? A systematic literature review of definitions and characteristics。Int J Qual Health Care，22，507-518。  new window
8.Pearson, T. F.、Pittman, D. G.、Longley, J. M.(1994)。Factors associated with preventable adverse drug reactions。Am J Hosp Pharm，51，2268-2272。  new window
9.Seeger, J. D.、Kong, S. X.、Schumock, G. T.(1998)。Characteristics associated with ability to prevent adverse drug reactions in hospitalized patients。Pharmacotherapy，18，1284-1289。  new window
10.Charles, K.、Cannon, M.、Hall, R.(2014)。Can utilizing a computerized provider order entry (CPOE) system prevent hospital medical errors and adverse drug events?。Perspect Health Inf Manag，11，1b。  new window
11.Koutkias, V. G.、McNair, P.、Kilintzis, V.(2014)。From adverse drug event detection to prevention. A novel clinical decision support framework for medication safety。Methods Inf Med，53，482-492。  new window
12.Forster, A. J.、Jennings, A.、Chow, C.(2012)。A systematic review to evaluate the accuracy of electronic adverse drug event detection。J Am Med Inform Assoc，19，31-38。  new window
13.Beeler, P. E.、Bates, D. W.、Hug, B. L.(2014)。Clinical decision support systems。Swiss Med Wkly，144，w14073。  new window
單篇論文
1.European Commission(2008)。Regulation of the European parliament and of the council amending, as regards pharmacovigilance of medicinal products for human use, regulation (EC) No 726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency and the directive of the European parliament and of the council amending, as regards pharmacovigilance, directive 2001/83/EC on the Community code relating to medicinal products for human use，http://ec.europa.eu/health/files/pharmacos/pharmpack_12_2008/pharmacovigilance-ia-vol1_en.pdf。  new window
 
 
 
 
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