问题 单项选择题 B1型题

初婚后要求长期避孕或再婚后不准备生育者()

A.以外用避孕药为宜,采用避孕阴茎套或外用避孕栓,以后可使用女性外用避孕药具如 * * 隔膜、避孕海绵、避孕药膜, * * 套等,也可采用自然避孕法,经济简便、安全、无害的优点,但单用此法易失败需谨慎

B.除可选用各种外用避孕药具外,如无用药禁忌可口服女用避孕药,以短效者为宜

C.探亲避孕药,避孕药需正确使用方可获高效。但必须注意,应在停药3~6个月才能受孕,以防影响胎儿

D.应选用长效、安全、简便、经济的避孕方法。如宫内节育器,长效避孕针、药、 * * 药环、皮下埋植等方法,也可根据具体情况选用。凡属终生不宜生育者,原则上有病一方应采取绝育或长效避孕措施

E.及早人工流产术

答案

参考答案:D

单项选择题 A型题
单项选择题

The “issues” reported were unthinkable. The physician who enrolled the most patients in the study, an Alabama weight-loss doctor, allegedly forged scores of signatures, enrolling “volunteers” every few minutes.

By the time of the FDA review, she was under criminal investigation. (She’s now in federal prison. ) Another key researcher had been put on probation by the California medical board for gross negligence. He was arrested shortly after the study ended, when police, called to his home on a domestic violence complaint, found him with a bag of cocaine and waving a loaded gun at imaginary people. The study was so riddled with fraud and error that FDA reviewers decided it was useless.

Yet Dr. Ross says he was told to reveal nothing about those problems to the advisory board, which recommended that the drug be approved. Later, he says, he was pressured to soften his report about Ketek’s liver toxicity to gain approval of higher-ups. Six million Americans have now used the drug, including hundreds of infants in a clinical trial designed to test Ketek’s effectiveness against ear infections. "How does one justify balancing the risk of fatal liver failure against one day less of ear pain" one FDA scientist, Rosemary Johann-Liang, protested—to no avail—in a memo to her superiors. Most ear infections clear up in a few days on their own, she says.

The agency says the controversy is overblown. "There was enough good, solid scientific data to make that decision. " Says FDA spokeswoman Julie Zawisza, pointing to what appeared to be a history of safe use of Ketek in other countries. Ketek has now been linked to 18 deaths and at least 134 cases of liver damage, according to an independent analysis using FDA data. The real toll, some researchers say, may be far greater.

Last October the FDA sent a warning letter to Sanofi-Aventis, Ketek’s maker, accusing the company of knowingly presenting compromised data to the agency, a charge the company denies. "We were not aware of the fraud," says spokeswoman Melissa Feltmann. "It was not until the FDA’s criminal investigators uncovered it that we became aware of it. "

The question remains, what did the FDA and the drugmaker know about the fake safety data, and when

Congressmen John Dingell and Bart Stupak, both Michigan Democrats, are investigating that mystery right now in Congressional hearings.

"Unfortunately. " Stupak says, "the truth comes too late for some victims. \

According to Paragraph 1, the Alabama physician was accused of().

A. forcing people to join his study

B. administering illegal drugs to patients

C. exaggerating some drug’s effects

D. inventing evidence for her research