Patient reporting of suspected adverse drug reactions: a review of published literature and international experience

被引:207
作者
Blenkinsopp, A. [1 ]
Wilkie, P.
Wang, M.
Routledge, P. A.
机构
[1] Univ Keele, Dept Med Management, Keele ST5 5BG, Staffs, England
[2] Cardiff Univ, Univ Coll Wales, Cardiff, Wales
关键词
adverse drug reactions (ADRs); consumers; patients; pharmacovigilance; reporting; side effects;
D O I
10.1111/j.1365-2125.2006.02746.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aims: To synthesize data from published studies and international experience to identify evidence of potential benefits and drawbacks of direct patient reporting of suspected adverse drug reactions (ADRs) by patients. Methods: Structured search of MEDLINE, CINAHL and PsycINFO supplemented by internet searches and requests for information to key contacts. Results: Seven studies (eight papers) were included in the review. None of the studies concerned spontaneous reporting by patients. Information on patient reporting systems was obtained for six countries, with summary data reported by four. Patient reports identified possible new ADRs that had not previously been reported by health professionals. The quality of patient reports appears to be similar to that of health professional reports. There is some evidence that patients report an ADR when they consider their health professional has not paid attention to their concerns. Patient reports may, at least initially, be more time consuming to process. Conclusions: Overall, the evidence indicates that patient reporting of suspected ADRs has more potential benefits than drawbacks. Evaluation of patient reporting systems is needed to provide further evidence.
引用
收藏
页码:148 / 156
页数:9
相关论文
共 33 条
[21]   Adverse drug reactions as cause of admission to hospital: prospective analysis of 18,820 patients [J].
Pirmohamed, M ;
James, S ;
Meakin, S ;
Green, C ;
Scott, AK ;
Walley, TJ ;
Farrar, K ;
Park, BK ;
Breckenridge, AM .
BMJ-BRITISH MEDICAL JOURNAL, 2004, 329 (7456) :15-19
[22]   Managing adverse drug reactions: time to get serious [J].
Roughead, EE .
MEDICAL JOURNAL OF AUSTRALIA, 2005, 182 (06) :264-265
[23]  
*ROYAL COLL GEN PR, 2006, 7 DAYS
[24]  
*SAF QUAL COUNC AU, 2004, CONS UPD
[25]   Reporting adverse drug reactions on a geriatric ward: a pilot project [J].
Somers, A ;
Petrovic, M ;
Robays, H ;
Bogaert, M .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2003, 58 (10) :707-714
[26]  
van Grootheest A C, 2005, Ned Tijdschr Geneeskd, V149, P529
[27]  
van Grootheest AC, 2004, EXPERT OPIN DRUG SAF, V3, P363
[28]   Consumer adverse drug reaction reporting - A new step in pharmacovigilance? [J].
van Grootheest, K ;
de Graaf, L ;
de Jong-van den Berg, LTW .
DRUG SAFETY, 2003, 26 (04) :211-217
[29]   Consumer groups look to improve adverse event reporting systems [J].
Vastag, B .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (24) :1804-1805
[30]  
Wiffen P., 2002, BANDOLIER EXTRA