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Adverse drug reactions monitoring: prospects and impending challenges for pharmacovigilance

机译:药物不良反应监测:药物警戒的前景和迫在眉睫的挑战

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摘要

Pharmacovigilance plays a consequential role in the surveillance of adverse drug reactions, which is provoked by the drugs used to cure diseases. Adverse drug reactions (ADRs) produce detrimental or undesirable effects to the body after administration of drugs. It has been reported that the number of patients dying because of contrary effects of drugs per year increased upto 2.6-fold. Moreover, rates of hospitalization of patients are increasing owing to adverse effects of drugs. Thus, it becomes challengeable for physician, health care providers, WHO and pharmaceutical industries to resolve the associated problem of ADRs. During the clinical trial of a novel drug, it is prominent to explore the dependability of drug. In this review, we documented the details required to identify the ADRs in patients along with reported banned drugs.
机译:药物警戒在药物不良反应的监测中起着重要作用,药物不良反应是由用于治疗疾病的药物引起的。药物不良反应(ADR)在给药后对人体产生有害或不良影响。据报道,每年由于药物的相反作用而死亡的患者人数增加了2.6倍。此外,由于药物的不良影响,患者的住院率正在增加。因此,对于医师,卫生保健提供者,WHO和制药行业来说,解决相关的ADR问题成为挑战。在新药的临床试验期间,探索药物的可靠性非常重要。在这篇综述中,我们记录了在患者中鉴定ADR所需的详细信息以及所报告的违禁药物。

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