期刊文献+
共找到1篇文章
< 1 >
每页显示 20 50 100
The Role of Medical Literature, Clinical Trials and Experimental Research in Drug Product-Injury Litigation: A Primer with Two Examples
1
作者 Jan M. Kitzen Joseph V. Pergolizzi Jr. +1 位作者 Robert Taylor Jr. Robert B. Raffa 《Pharmacology & Pharmacy》 2018年第6期208-227,共20页
When any type of product has been ordered to be removed from the marketplace by a governmental regulatory body, that action is a powerful indicator that the product has been determined to be unsafe for further use, th... When any type of product has been ordered to be removed from the marketplace by a governmental regulatory body, that action is a powerful indicator that the product has been determined to be unsafe for further use, thereby branding the product as defective and opening up the possibility of product liability litigation. When the product is a drug or medical device, it is especially serious since the possibility of personal injury (acute and/or chronic) or death may occur. Needless to say, in these situations, product injury litigation will almost surely follow. We review the definition and requisite claims needed to establish drug product liability, and the role that the medical literature, clinical trial data, and even experimental research data can play in product (drug)-injury litigation. We show how each of these resources played a significant role in two well-known cases: Fen-Phen and thimerosal. The ultimate goal of such knowledge is to make better informed decisions about drug safety. 展开更多
关键词 DRUG Safety PRODUCT Quality INJURY LITIGATION fen-phen THIMEROSAL
暂未订购
上一页 1 下一页 到第
使用帮助 返回顶部