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  3. The "issues" reported were unthinkable. The physician who enrolled the most

The "issues" reported were unthinkable. The physician who enrolled the most

游客2025-04-16  3
问题     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 u-sing 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. " [br] FDA suspected Sanofi-Aventis of______.
选项 A、being unqualified to make drugs
B、scheming to do the fraud
C、letting the misconduct go
D、being unaware of the crime
答案 B
解析 本题考查细节辨认。第六段第一句：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．句意为：去年十月份，食品和药品管理局给肯立克制药商赛诺菲安万特公司发了一封警告信，指控该公司故意改写了相关数据。据此可知，食品及药品管理局怀疑赛诺菲安万特有意欺骗，所以B项符合题意。
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