POSTMARKETING SURVEILLANCE OF THE SAFETY OF CIMETIDINE - 10 YEAR MORTALITY REPORT

被引:45
作者
COLINJONES, DG
LANGMAN, MJS
LAWSON, DH
LOGAN, RFA
PATERSON, KR
VESSEY, MP
机构
[1] RADCLIFFE INFIRM, DEPT PUBL HLTH & PRIMARY CARE, OXFORD OX2 6HE, ENGLAND
[2] GLASGOW ROYAL INFIRM, GLASGOW G4 0SF, SCOTLAND
[3] UNIV NOTTINGHAM HOSP, NOTTINGHAM NG7 2UH, ENGLAND
[4] UNIV STRATHCLYDE, GLASGOW G1 1XW, SCOTLAND
[5] QUEEN ELIZABETH HOSP, BIRMINGHAM B15 2TH, W MIDLANDS, ENGLAND
[6] QUEEN ALEXANDRA HOSP, PORTSMOUTH, HANTS, ENGLAND
关键词
D O I
10.1136/gut.33.9.1280
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
A total of 9928 cimetidine users were identified from prescriptions in four centres and followed for 10 years. The 'all-cause' mortality ratio fell from 1-9 in year 1 to 1.0 in years 8 to 10. Most of the early excess in mortality was attributable to cimetidine being given in the late stages of many diseases, often to counter adverse gastric effects of other drugs. Specific causes of mortality during years 5-10 of the study, were generally unremarkable. Significant increases in mortality ratios were apparent, however, for oesophageal cancer (years 5-7, 2.3; years 8-10, 1.9); lung cancer (years 5-7, 1.1; years 8-10, 1.7); diseases of the oesophagus, stomach, and duodenum (years 5-7, 3.3; years 8-10, 2.3); and chronic liver disease (years 5-7, 2-4; years 8-10, 3.3). None of these increases in mortality seems to be attributable to an adverse effect of cimetidine use. Data are also presented for mortality from diseases of the nervous system. Eight deaths (of which one was miscoded) were certified as being from motor neurone disease, representing a mortality ratio of 2.6 for years 2-10 of the study which is of borderline statistical significance. This study confirms that cimetidine is safe. Mortality from some diseases increased over the study period, but selection rather than any adverse effect of the drug is likely to be the explanation.
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页码:1280 / 1284
页数:5
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