毒品问题还是医疗犯罪?伪造曲马多药物在埃及和西非的分布和使用

Q3 Social Sciences Journal of illicit economies and development Pub Date : 2019-01-14 DOI:10.31389/JIED.10
A. Klein
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引用次数: 27

摘要

曲马多是一种合成阿片类药物,广泛用作缓解中度至中度疼痛的止痛药。曲马多的药效估计约为吗啡的十分之一,因此被认为对中毒或依赖性相对安全。然而,越来越多的报告称,在北非和西非,曲马多的非医疗消费普遍存在。埃及政府已要求联合国麻醉药品委员会对曲马多进行国际管制。这将对发展中国家的急性和慢性疼痛的治疗产生深远影响,在这些国家,曲马多通常是唯一可用的止痛药,因为医护人员不可能获得受控物质。在医疗机构外销售的曲马多往往是掺假和不合格的,这是假药大规模交易的一部分,可能比精神活性物质的享乐使用更具破坏性。然而,控制医疗产品的国际机制薄弱,对医疗犯罪的处罚与贩毒犯罪相比也不算严厉。文章建议,国际管制需要重新评估其优先事项,以关注人类和患者的福祉。需要进一步转变,从对消费者的镇压措施转向对药物和药物的生产和分销进行更严格的监管。这必须涉及广泛的利益相关者,包括医疗从业者、制药行业、药剂师、患者协会和广大公众。
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Drug Problem or Medicrime? Distribution and Use of Falsified Tramadol Medication in Egypt and West Africa
Tramadol is a synthetic opioid that is widely used as an analgesic for alleviating pain of moderate to medium intensity. With potency estimated to be about one-tenth that of morphine, tramadol is considered as relatively safe with regard to poisonings or dependency. Yet there are increasing reports of widespread non-medical consumption of tramadol in North and West Africa. The Egyptian government has requested the UN Commission of Narcotic Drugs to put tramadol under international control. This will have profound implications for the treatment of acute and chronic pain across developing countries where tramadol is often the only available analgesic, because controlled substances are impossible to obtain for health care practitioners. The tramadol sold outside of medical establishments is often adulterated and substandard, part of the massive trade in falsified medicines that is possibly far more devastating than the hedonic use of psychoactive substances. Yet the international machinery in place to control medical products is feeble and the penalties for medicrime are modest next to drug trafficking offences. The article suggests that international controls need to re-assess their priorities to focus on human and patient well-being. A further shift is needed away from repressive measures against consumers, to tighter regulation in the production and distribution of medications and pharmaceutical substances. This must involve a wide range of stakeholders, including health care practitioners, the pharmaceutical industry, pharmacists, patients associations, and the public at large.
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38 weeks
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