首页
登录
职称英语
Growing concerns over the safety and efficacy of anti-depressant drugs presc
Growing concerns over the safety and efficacy of anti-depressant drugs presc
游客
2024-12-29
18
管理
问题
Growing concerns over the safety and efficacy of anti-depressant drugs prescribed to children have caught the eye of Congress and the New York state attorney general. Now they’re becoming the catalyst for calls to reform the way clinical trials of all drugs are reported.
Pressure is already causing some changes within the pharmaceutical industry. And it has put the US Food and Drug Administration (FDA), which approves new drugs, in the hot seat. If reforms are carried out, they could bring an unprecedented level of transparency to drug research.
The solution now under consideration: a public database, or registry, of drug trials, where companies would post the results of those trials.
In congressional testimony Thursday, a spokesman for the American Medical Association endorsed the registry and said it should include information on each trial’s purpose and objective, its design, and the dates it begins and ends. If the trial is not completed, the registry should include an explanation.
While drug companies have been eager to make public any positive results of their trials, recent revelations suggest they’ve balked at divulging tests when the results are not what they’d hoped to see. The furor has centered around the use Of anti-depressants on children.
The industry has begun to make some moves to address the concerns about drug trials. Drug companies have agreed to set up a voluntary system of posting their drug trials on the Internet. But that seems unlikely to satisfy some members of Congress, who are expected to introduce legislation to establish a mandatory drug registry.
Last week, editors of a dozen influential medical journals announced that they would begin requiring drug companies to post a drug trial in a public database prior to accepting an article about it. Doctors rely on these articles to make treatment choices. The editors hope that the registry will force unfavorable drug studies, before kept secret, into the open.
Medical journals already had been tightening up on the authorship of their articles, insisting that authors declare if they had any conflicts of interest, such as any financial or other ties to the drug company, says Daniel Callahan, a director at the Hastings Center, a nonprofit bioethics research institute in Garrison, N.Y.
Information from previously undisclosed clinical trials could lower prices, reduce the number of badly designed trials, and help doctors considering the use of a drug for a non-approved purpose to know why it hasn’t been approved for that use.
Antidepressant drugs "have some serious side effects ... that seem to be much more common than people realize ... much more common than you might think from seeing drug ads and from reports on drug studies," says Joel Gurin, executive vice president of Consumer Reports. His magazine just finished a survey of readers showing a "dramatic shift from talk therapy to drug therapy for mental health problems" during the past decade. In 1995, less than half of people getting mental health treatment--40 percent--got drug therapy. Today 68 percent receive drug treatment, Mr. Gurin says.
Some studies coming to light show that antidepressants work no better than placebos. Even better than merely registering drug trials, Caplan (director of the Center for Bioethics at the University of Pennsylvania in Philadelphia) suggests, would be to require that a new drug not only be "safe and do what it’s supposed to do", but that it do it as well or better than other drugs already on the market. That, he says, would help push research into new areas and save money. [br] Which of the following statements is true about drug companies?
选项
A、They are very transparent in reporting the results of the tests.
B、They have reached an agreement with Congress.
C、Sometimes they hold back unfavorable results.
D、They are willingly to post a drug trial in a public database.
答案
C
解析
下面哪一项关于药品公司的论述是ten龟的?第五段提到“recent revelations suggest they’ve balked at divulging tests when the results are not what they’d hoped to see”即,药品公司会隐瞒那些对自己不利的结果。
转载请注明原文地址:https://www.tihaiku.com/zcyy/3890137.html
相关试题推荐
Asitconcernssomanypeople’sprivacy,Iwouldappreciateyoukeepitasecret
Recently,onlineshoppinghasbeengaininggrowingpopularityinChina.Prop
WhichofthefollowingisTRUEaboutthesafetyofputtingphotosonline?[br]
WhichofthefollowingisTRUEaboutthesafetyofputtingphotosonline?[br]
WeliveinsouthernCaliforniagrowinggrapes,afirstgenerationofvintner
WeliveinsouthernCaliforniagrowinggrapes,afirstgenerationofvintner
WeliveinsouthernCaliforniagrowinggrapes,afirstgenerationofvintner
WeliveinsouthernCaliforniagrowinggrapes,afirstgenerationofvintners
WeliveinsouthernCaliforniagrowinggrapes,afirstgenerationofvintners
WeliveinsouthernCaliforniagrowinggrapes,afirstgenerationofvintners
随机试题
AlthoughshedidnotknowBostonwell,shemadeherway______totheHomeCircle
ImaginesendingelectronicmailtoyourfriendintheU.S.ordiscussingyour
A.呆小病 B.黏液性水肿 C.甲状腺危象 D.甲状腺功能检查 E.单纯
在锚具静载锚固性能试验过程中,应按照预应力钢绞线抗拉强度标准值(80%?ptk)
______学校不得聘任这类人员担任教师。
阳虚证应采用的治法是A.寒者热之B.热者寒之C.阳病治阴D.阴病治阳E.寒因寒用
质量问题是以质量损失的形式表现出来的,大多数损失往往是由()不合格引起的,这些
具有低成本扩散与收益放大效应、协同整合效应、风险分散效应、技术导向效应、自我催化
改革开放以来,我国一直积极发展对外贸易。贸易的一个主要好处是它允许国家间()
非组织化观摩要求观摩者有相当完备的()和(),否则难以达到
最新回复
(
0
)