药品稳定性与临床用药安全息息相关,是临床用药安全的根本保障。普遍而言,药品的储存时间与其化学降解程度成正比,储存时间越长,药品中有效成分越少,有害物质不断增加,对临床用药而言,具有巨大的安全风险。对药品稳定性进行深入了解并准确掌握,不仅可以确保临床用药具有较高的安全性,还可以为药品生产经营活动的各个环节提供有价值的信息,例如,销售、生产以及研制等。 Drug stability and clinical drug safety is closely related to the fundamental protection of clinical drug safety. In general, the storage time of a drug is directly proportional to the degree of its chemical degradation. The longer the storage time, the fewer effective components in the drug and the increasing of harmful substances, which pose a huge safety risk for clinical use. In-depth understanding of drug stability and accurate grasp, not only to ensure that clinical medication with high safety, but also for all aspects of pharmaceutical production and management activities to provide valuable information, such as sales, production and development.