Jones D G, Langman M J, Lawson D H, Vessey M P
Queen Alexandra Hospital, Portsmouth, Hampshire, UK.
Aliment Pharmacol Ther. 1987 Jun;1(3):167-77. doi: 10.1111/j.1365-2036.1987.tb00616.x.
Experience obtained during post-marketing surveillance of the safety of cimetidine emphasizes the difficulties in interpretation posed by the high background frequency of disease of all types in drug takers. The multiple sources of confounding factors, and their high prevalence, make it impossible to detect adverse events which mimic ordinary disease, particularly when a consistent relationship between adverse event and drug exposure is not observed. The inclusion of controls emphasizes the difficulties but does not ease interpretation.
西咪替丁上市后安全性监测所获得的经验凸显了在解释服药者中各类疾病高背景发生率所带来的困难。混杂因素的多种来源及其高发生率使得无法检测出酷似普通疾病的不良事件,尤其是在未观察到不良事件与药物暴露之间存在一致关系的情况下。纳入对照凸显了困难,但并未简化解释。