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药品是开展疾病预防和治疗工作的基本要素,在保证人民群众生命和健康安全方面发挥着重要的作用。但是药品本身也具有不同程度的药性和毒性,如果药品质量不合格或者成分配备不科学,就可能会导致用药事故的发生。近年来,我国发生了多起药害时间,这除了药品本身的质量问题,与药品市场管理混乱也有着密切的关系,假冒伪劣药品流入市场,对药品市场的秩序产生了不良影响,也为用药安全埋下了安全隐患。基于此,本文就主要针对假冒伪劣药品的监督与管理等问题进行简单的探讨。
Drugs are an essential element in disease prevention and treatment and play an important role in ensuring the lives and health and safety of the people. However, the drug itself has varying degrees of toxicity and toxicity. If the quality of the drug is unqualified or the ingredients are unscientific, it may lead to the occurrence of medication accidents. In recent years, there have been many injury-injuring times in our country. In addition to the quality problems of the drugs themselves, there is a close relationship with the chaotic pharmaceutical market management. The inflow of counterfeit and inferior drugs into the market has an adverse effect on the order of the pharmaceutical market, Safety laid a security risk. Based on this, this article mainly focuses on the supervision and management of counterfeit drugs and other issues a simple discussion.