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
医学
Without fanfare or legislation, the government is orchestrating a quiet revolution in how it regulates new medicines. The revolu
Without fanfare or legislation, the government is orchestrating a quiet revolution in how it regulates new medicines. The revolu
admin
2013-11-30
31
问题
Without fanfare or legislation, the government is orchestrating a quiet revolution in how it regulates new medicines. The revolution is based on the idea that the sicker people are, the more freedom they should have to try drugs that are not yet fully tested. For fifty years government policy has been driven by another idea; the fear that insufficiently tested medicines could cause deaths and injuries. The urgent needs of people infected with HIV, the AIDS virus, and the possibility of meeting them with new drugs have created a compelling countervailing force to the continuing concern with safety. As a result, government rules and practices have begun to change. Each step is controversial. But the shift has already gone far beyond AIDS. New ways are emerging for very sick people to try some experimental drugs before they are marketed. People with the most serious forms of heart disease, cancer, emphysema, Alzheimer’ s or Parkinson’ s disease, multiple sclerosis, epilepsy , diabetes, or other grave illnesses can request such drugs through their doctors and are likelier to get them than they would have been four years ago. " We’ ve been too rigid in not making life-saving drugs available to people who otherwise face certain death," says Representative Henry Wax-man, of California, who heads the subcommittee that considers changes in drug-approval policies. "It’ s true of AIDS, but it’ s also true of cancer and other life-threatening diseases. "
For the first time, desperate patients have become a potent political force for making new medicines available quickly. People with AIDS and their advocates, younger and angrier than most heart-disease or cancer patients, are drawing on two decades of gay activists’ success in organizing to get what they want from politicians. At times they found themselves allied with Reagan Administration deregulators, scientists, industry representatives, FDA staff members, and sympathetic members of Congress. They organized their own clinical trials and searched out promising drugs here and abroad. The result is a familiar Washington story; a crisis—AIDS—helped crystallize an informal coalition for reform.
AIDS gave new power to old complaints. As early as the 1970s the drug industry and some independent authorities worried that the Food and Drug Administration’ s testing requirements were so demanding that new drugs were being unreasonably delayed. Beginning in 1972, several studies indicated that the United States had lost its lead in marketing new medicines and that breakthrough drugs, those that show new promise in treating serious or life—threatening diseases—had come to be available much sooner in other countries. Two high-level commissions urged the early release of breakthrough drugs. So did the Carter Administration, but the legislation it proposed died in Congress. Complaints were compounded by growing concern that "if we didn’ t streamline policies, red tape would be an obstacle to the development of the biotechnology revolution," as Frank E. Young, who was the head of the FDA from 1984 to 1989, put it in an interview with me.
Young was a key figure in the overhaul of the FDA’ s policies. A pioneer in biotechnology and a former dean of the University of Rochester’ s medical school, he came to Washington with an agenda and headed the agency for five and a half years—longer than anyone else has since the 1960s. Young took the FDA job to help introduce new medicines created by biotechnology—whose promise he had seen in his own gene-cloning lab and to get experimental medicines to desperately ill people more quickly. He had seen people die waiting for new medicines because " they were in the wrong place at the wrong time," he said. That is now changing.
It can be said that the people who first started the quiet drug revolution are______.
选项
A、doctors
B、government officials
C、AIDS patients
D、pharmacologists
答案
C
解析
第一段指出The revolution is based on the idea that the sicker people are…try drugs thatare not yet fully tested,表明对那些严重的病人来说,一种新药就是一线生机,因此他们才是这场药品变革的倡导者,选项C正确。
转载请注明原文地址:https://kaotiyun.com/show/rtU3777K
本试题收录于:
医学博士外语题库考研分类
0
医学博士外语
考研
相关试题推荐
Severalclassesofbittercitruscompoundhavelookedpromisingasanticanceragentsinlaboratorytests.Anewstudyindicates
A、Shewasknockeddownbyafeather.B、SheisshamedofLarry.C、Shewasreallysurprised.D、ShewasproudofLarry.C女士听到消息后说的话
A、Canceltheweddingimmediately.B、Findasubstituteimmediately.C、Waitpatientlytillthegroomtocomefinally.D、Findalaw
A、Thedifferencebetweenthecoupleintheirviewoftime.B、Thedifferencebetweenthecoupleintheirviewofreligion.C、The
The______conditionsandplacesarelikelytocausediseases.
Shyness,themostcommonformofsocialanxiety,occurswhenaperson’sapprehensionsaresogreatthattheyinhibithismaking
Workisa______ofsatisfaction.
Iworkedtodeveloptherequisiteskillforamanagerial.
Cityofficialsstatedthatworkerswholiedontheiremploymentapplicationsmaybeterminated.
ItissaidthatinEnglanddeathispressing,inCanadainevitableandinCaliforniaoptional.Smallwonder.Americans’lifeexp
随机试题
抗阿米巴药物中毒性最大的是
患者,男,40岁。舌侧倾斜较大,最佳的设计方案是
普萘洛尔与哪种药合用,可相互抵消不良作用,提高疗效?()
导游为旅游者提供心理服务的基本要求是()。
儿童龋齿的预防措施有哪些?
甲从A地到B地需要30分钟,乙从B地到A地需要45分钟,甲乙两人同时从A、B两地相向而行,中间甲休息了20分钟,乙也休息了一段时间,最后两人在出发40分钟后相遇。问乙休息了多少分钟?()
小美三年前收藏的古董花瓶市价上涨了30%,为了尽快出手,她告诉中介,一周内购买的买家其成交价可以比现在的市价再便宜5万元,并且可以在1万中介费的基础上,再多支付5000元给中介。最终在一周内以60万元的价格成交,那么,小美的古董花瓶赚了多少万元?(
(07年)设二维随机变量(X,Y)的概率密度为(I)求P{X>2Y);(Ⅱ)求Z=X+Y的概率密度fZ(z).
函数的值域区间是___________.
有一个NAT设备具有一个外部IP地址,如果内部的5台主机都希望利用该外部IP地址同时访问Internet,那么该设备应该采用的工作模式为()。
最新回复
(
0
)