Safety profile of esomeprazole - Results of a prescription-event monitoring study of 11595 patients in England

被引:17
作者
Davies, Miranda [1 ]
Wilton, Lynda V. [1 ,2 ]
Shakir, Saad A. W. [1 ,2 ]
机构
[1] Drug Safety Res Unit, Southampton SO31 1AA, Hants, England
[2] Univ Portsmouth, Portsmouth, Hants, England
关键词
D O I
10.2165/00002018-200831040-00005
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Objective: Esomeprazole, the S-isomer of omeprazole, was launched in the UK in September 2000. The first proton pump inhibitor, omeprazole, has been marketed in the UK for over 10 years. However, the adverse event database of newly marketed drugs is limited, and it is only after widespread clinical use that the adverse effect profile of a drug is ascertained more comprehensively. This study aims to monitor the safety of esomeprazole prescribed in the primary care setting in England using prescription-event monitoring (PEM). Methods: A postmarketing surveillance study using the observational cohort technique of PEM. Patients were identified from dispensed prescriptions for esomeprazole issued by general practitioners between September 2000 and April 2001. Questionnaires ('green forms') requesting clinical event data on these patients were sent to prescribers approximately 6 months after the date of the first dispensed prescription for each individual patient. Incidence densities (IDs), expressed as the number of first reports of an event/1000 patient-months of exposure (PME), were calculated. Significant differences between IDs for events reported in the first month (ID1) and the following 5 months (ID2-6) of exposure were regarded as potential signals. Other methods for signal detection such as medical evaluation of selected events and evaluation of reasons for stopping were also applied. Results: Green forms containing clinically useful information for 11595 patients (median age 56 years; 53.2% female) were received. Diarrhoea was the event with the highest ID1 in month 1 (8.0 per 1000 patient months of exposure). Adverse events that occurred significantly more often in the first month of treatment with esomeprazole compared with months 2-6 included diarrhoea, nausea/vomiting, abdominal pain, dyspepsia, headache/migraine, intolerance, malaise/lassitude, pruritis, unspecified adverse effects and abnormal sensation. Conclusions: The safety profile of esomeprazole was consistent with the prescribing information and experience reported in the literature.
引用
收藏
页码:313 / 323
页数:11
相关论文
共 29 条
[1]  
[Anonymous], 2002, Pharmacovigilance
[2]  
*ASTRAZENECA, 2000, NEX ES
[3]  
*ASTRAZENECA, 2003, NES ES
[4]   Mortality study of 18 000 patients treated with omeprazole [J].
Bateman, DN ;
Colin-Jones, D ;
Hartz, S ;
Langman, M ;
Logan, RF ;
Mant, J ;
Murphy, M ;
Paterson, KR ;
Rowsell, R ;
Thomas, S ;
Vessey, M .
GUT, 2003, 52 (07) :942-946
[5]  
Castell DO, 2002, AM J GASTROENTEROL, V97, P575
[6]  
Cioms/Who, 2002, INT GUID BIOM RES IN
[7]  
*DEP HLTH, 2000, SUPPL OP GUID NHS RE
[8]   Use of omeprazole during pregnancy -: no hazard demonstrated in 955 infants exposed during pregnancy [J].
Källén, BAJ .
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2001, 96 (01) :63-68
[9]   The safety of omeprazole during pregnancy: A multicenter prospective controlled study [J].
Lalkin, A ;
Loebstein, R ;
Addis, A ;
Ramezani-Namin, F ;
Mastroiacovo, P ;
Mazzone, T ;
Vial, T ;
Bonati, M ;
Koren, G .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1998, 179 (03) :727-730
[10]  
Lessell S, 1998, BRIT MED J, V316, P67