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Differences between the European Union and United States of America in Drug Regulatory Affairs Affect Global Patient Safety Standards and Public Health Awareness: The Case of Deferasirox and Other Iron Chelating Drugs

机译:欧盟和美国在药物监管事务方面的差异影响了全球患者安全标准和公共卫生意识:脱铁司和其他铁螯合药物的情况

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摘要

Regulatory policies on drugs have a major impact on patient safety and survival. Some pharmaceutical companies employ all possible methods to achieve maximum sales in relation to the monopoly of their patented drugs, leading sometimes to irregularities and illegal activities. Misinformation on the orphan drug deferasirox has reached the stage of criminal investigations and fines exceeding USD 100 million. Additional lawsuits of USD 3.5 billion for damages and civil fines were also filed by the FBI of the USA involving deferasirox and mycophenolic acid, which were later settled with an additional fine of USD 390 million. Furthermore, a USD 345 million fine was also settled for bribes and other illegal overseas operations including an EU country. However, no similar fines for illegal practises or regulatory control violations have been issued in the EU. Misconceptions and a lack of clear guidelines for the use of deferasirox in comparison to deferiprone and deferoxamine appear to reduce the effective treatment prospects and to increase the toxicity risks for thalassaemia and other iron loaded patients. Similar issues have been raised for the activities of other pharmaceutical companies promoting the use of new patented versus generic drugs. Treatments for different categories of patients using new patented drugs are mostly market driven with no clear safeguards or guidelines for risk/benefit assessment indications or for individualised effective and safe optimum therapies. There is a need for the establishment of an international organisation, which can monitor and assess the risk/benefit assessment and marketing of drugs in the EU and globally for the benefit of patients. The pivotal role of the regulatory drug authorities and the prescribing physicians for identifying individualised optimum therapies is essential for improving the survival and safety of millions of patients worldwide.
机译:药物的监管政策对患者安全和生存产生了重大影响。一些制药公司聘请了所有可能的方法,以实现与其专利药物的垄断有关的最大销售,有时甚至是违规行为和非法活动。孤儿药物Deferasir的错误信息已达到刑事调查阶段,罚款超过1亿美元。美国FBI涉及脱司索和霉菌酸的美国联邦调查局提出了35亿美元的额外诉讼,后来稳定,额外罚款3.9亿美元。此外,为贿赂和其他非法海外业务提供3.45亿美元的罚款,包括欧盟国家。但是,欧盟未发出非法行为或监管违规行为的类似罚款。与Deferiprone和Deferoxamine相比,使用脱铁司途径的误解和缺乏明确指南似乎减少了有效的治疗前景,并增加了血症和其他铁的毒性风险。其他制药公司的活动提出了类似的问题,促进使用新专利与普通药物的使用。使用新的专利药物的不同类别患者的治疗主要是市场驱动,没有明确的风险/福利评估指示或个性化有效和安全的最佳疗法的可靠性或指导方针。需要建立一个国际组织,可以监测和评估欧盟和全球毒品的风险/效益评估和销售患者的利益。监管药物当局和规定个性化最优疗法的处方医师的关键作用对于提高全球数百万患者的存活和安全至关重要。

著录项

  • 期刊名称 Medicines
  • 作者

    George J. Kontoghiorghes;

  • 作者单位
  • 年(卷),期 2021(8),7
  • 年度 2021
  • 页码 36
  • 总页数 17
  • 原文格式 PDF
  • 正文语种
  • 中图分类 药学;
  • 关键词

    机译:专利的药物;脱硫;脱铁酮;德国毒液;道德;监管事务;患者安全;药物疗效;孤儿药;营销;公共卫生;公共卫生;

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