首页
外语
计算机
考研
公务员
职业资格
财经
工程
司法
医学
专升本
自考
实用职业技能
登录
外语
Under existing law, a new drug may be labeled, promoted, and advertised only for those conditions in which safety and effectiven
Under existing law, a new drug may be labeled, promoted, and advertised only for those conditions in which safety and effectiven
admin
2012-03-23
49
问题
Under existing law, a new drug may be labeled, promoted, and advertised only for those conditions in which safety and effectiveness have been demonstrated and of which the Food and Drug Administration (FDA) has approved, or so- called "approved uses. " Other uses have come to be called "unapproved uses" and cannot be legally promoted. In a real sense, the term "unapproved" is a misnomer because it includes in one phrase two categories of marketed drugs that are very different; drugs which are potentially harmful and will never be approved, and already approved drugs that have "unapproved" uses. It is common for new research and new insights to demonstrate valid new uses for drugs already on the market. Also, there are numerous examples of medical progress resulting from the serendipitous observations and therapeutic innovations of physicians, both important methods of discovery in the field of therapeutics. Before such advances can result in new indications for inclusion in drug labeling, however, the available data must meet the legal standard of substantial evidence derived from adequate and well-controlled clinical trials. Such evidence may require time to develop, and, without initiative on the part of the drug firm, it may not occur at all for certain uses. However, because medical literature on new uses exists and these uses are medically beneficial, physicians often use these drugs for such purposes prior to FDA review or changes in labeling. This is referred to as "unlabeled uses" of drugs.
A different problem arises when a particular use for a drug has been examined scientifically and has been found to be ineffective or unsafe, and yet physicians who either are uninformed or who refuse to accept the available scientific evidence continue to use the drug in this way. Such use may have been reviewed by the FDA and rejected, or, in some cases, the use may actually be warned against in the labeling. This subset of uses may be properly termed "disapproved uses. "
Government policy should minimize the extent of unlabeled uses. If such uses are valid—and many are—it is important that scientifically sound evidence supporting them be generated and that the regulatory system accommodate them into drug labeling. Continuing rapid advances in medical care and the complexity of drug usage, however, makes it impossible for the government to keep drug labeling up to date for every conceivable situation. Thus, when a particular use of this type appears, it is also important, and in the interest of good medical care, that no stigma be attached to "unapproved usage" by practitioners while the formal evidence is assembled between the time of discovery and the time the new use is included in the labeling. In the case of "disapproved uses," however, it is proper policy to warn against these in the package insert, whether use of a drug for these purposes by the uninformed or intransigent physician constitutes a violation of the current Federal Food, Drug and Cosmetic Act is a matter of debate that involves a number of technical and legal issues. Regardless of that, the inclusion of disapproved uses in the form of contraindications, warnings and other precautionary statements in package inserts is an important practical deterrent to improper use. Except for clearly disapproved uses, however, it is in the best interests of patient care that physicians not be constrained by regulatory statutes from exercising their best judgment in prescribing a drug for both its approved uses and any unlabeled uses it may have.
Which of the following is true with disapproved drugs?
选项
A、There is nothing to prove that such drugs are not safe.
B、It is affirmative that such drugs are ineffective and dangerous.
C、Physicians do not intend to use such drugs.
D、Such drugs have never been tested by FDA.
答案
B
解析
细节判断题。在文章第二段中,作者提到在药品使用过程中会出现一些问题,如有些药被检测无效或不安全,但有些医生不知情或不接受检测结果而继续使用此类药物。因此,只有答案B是正确的。其它选项与文章意思相反,故不正确。
转载请注明原文地址:https://kaotiyun.com/show/5oiO777K
0
专业英语八级
相关试题推荐
IntheAustralianstateofNewSouthWales,agovernmentsponsorsurveyrevealedsomeshockingstatisticsregarding【1】_
MostpeoplethinkoflionsasstrictlyAfricanbeasts,butonlybecausethey’vebeenkilledoffalmosteverywhereelse.Tenthou
Duringthefirsthalfoftheseventeenthcentury,whenthenationsofEuropewerequarrelingoverwhoownedtheNewWorld,theD
Specialisationcanbeseenasaresponsetotheproblemofanincreasingaccumulationofscientificknowledge.Bysplittingupt
Haveyoueverthoughtofthesimilaritiesbetweenthecinemaandthetheatre?Thecinemahaslearntagreatdealfromthetheat
In1981KenjiUrada,a37-year-oldJapanesefactoryworker,climbedoverasafetyfenceataKawasakiplanttocarryoutsomema
UsingComputersOurcollegeisnowequippedwiththemost【1】teachingaidsandafirst-classcomputercentre.Wehaveplansto
TheFutureofPCMarketThefirstDevelopersConferenceinChinamarksamajormilestoneforMicrosoft,becausethesuccesso
Heiswaitingfortheairlineticketcounterwhenhefirstnoticestheyoungwoman.Shehasglossyblackhairpulledtightlyint
随机试题
若广义积分∫1+∞dx收敛,则p应满足().
颌骨骨折复位成功的标志是
患者,男,35岁,春节期间突患急性胆囊炎,症见胁痛,口苦,舌红苔黄。证属肝胆湿热,医师依据其要求,给其处以方便服用的消炎利胆颗粒。医师处以消炎利胆颗粒,此因其功能是()。
护士为病人鼻饲时,下列哪项是错误的()
治疗支原体肺炎的首选抗生素是()。
下列关于清算组职能的叙述,正确的是()。
设立工程咨询企业法人的一般程序有()。
2016年,习近平总书记在宁夏考察时指出“发展全域旅游,路子是对的,要坚持走下去”;2017年和2018年连续两年的国务院政府工作报告中均对发展全域旅游做出了部署安排;2018年国务院专门出台《关于促进全域旅游发展的指导意见》,这些都充分表明全域旅游已成为
“汇率超调论”是美国麻省理工学院教授_________于1976年提出的。(南开大学2000)
某文本型字段的值只能是字母且不允许超过6个,则可将该字段的输入掩码属性定义为
最新回复
(
0
)