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基于真实世界SRS数据的仙灵骨葆制剂不良反应分析

[Analysis of adverse reactions of Xianling Gubao preparation based on real world SRS data].

作者信息

Peng Shi-Yu, Xie Yan-Ming, Wang Zhi-Fei, Zhang Yi-Li, Yi Dan-Hui

机构信息

Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences Beijing 100700, China Beijing Tongzhou District Combine Traditional Chinese and Western Medicine Hospital Beijing 101100, China.

Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences Beijing 100700, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2020 May;45(10):2316-2321. doi: 10.19540/j.cnki.cjcmm.20200211.505.

Abstract

From January 1, 2004 to July 21, 2016 a total of 2 796 cases of adverse drug reaction/adverse event(ADR/AE) after the use of Xianling Gubao Capsules/Tablets were reported by National Adverse Drug Reaction Monitoring Center. The following results were obtained by analyzing the reports of 2 796 cases of adverse drug reactions/adverse drug events after the use of Xianling Gubao Capsules/Tablets. A total of 75 patients, accounting for 2.68% of the total ADR/AE time, had severe ADR/AE events. Among them, 30 patients were aged 65 and above, accounting for 40.00% of the total number of severe ADR/AE patients. All the patients with ADR/AE were aged 45-64 years, which totaled 1 346 cases and took up 48.14% of the total patients with ADR/AE. All of ADR/AE cases and severe ADR/AE cases were orally given Xianling Gubao Capsules/Tablets. Females accounted for 52.50% and 76.00%, respectively, and the proportion of females was significantly higher than that of males. Among patients with a medical history of ADR/AE, severe ADR/AE was higher than the average, accounting for about 1.33%. The proportion of cases orally given 1-3 tablets of Xianling Gubao Capsules/Tablets in all ADR/AE cases and severe ADR/AE cases was 95.32% and 96.00%, which conformed to the usage in the package insert. All ADR/AE cases and severe ADR/AE cases orally given Xianling Gubao Capsules/Tablets twice daily occupied the highest proportions, or 77.00% and 61.00%, respectively. The proportion of severe ADR/AE cases orally given Xianling Gubao Capsules/Tablets was slightly higher than that of all ADR/AE cases in the medication frequency, which didn't conform to the usage in the package insert. All the symptoms of ADR/AE orally given Xianling Gubao Capsules showed many manifestations, and the top 10 symptoms were nausea, rash, itching, stomach dysfunction, vomiting, abdominal pain, dizziness, diarrhea, anaphylaxis, and reflux heartburn. The symptoms of severe ADR/AE after oral administration of Xianling Gubao Capsules were varied, and the top 10 symptoms were abnormal liver function, rash, suffocation, itching, dizziness, vomiting, anaphylaxis, abdominal pain, weakness, and convulsions. Abnormal liver function accounted for 44.12%. All of ADR/AE cases occurred within 2 days after oral administration of Xianling Gubao Capsules/Tablets, accounting for 54.26%. Severe ADR/AE occurred within 2 days after the use of Xianling Gubao Capsules/Tablets, accounting for 25.34%. The proportion of ADR/AE cases occurring within 15 days after oral administration of Xianling Gubao Capsules/Tablets increased again(57.33%). The overall trend contained two peaks.

摘要

2004年1月1日至2016年7月21日,国家药品不良反应监测中心共收到2796例仙灵骨葆胶囊/片使用后药品不良反应/不良事件(ADR/AE)报告。通过对2796例仙灵骨葆胶囊/片使用后药品不良反应/不良事件报告进行分析,得出以下结果。共有75例患者发生严重ADR/AE事件,占ADR/AE总数的2.68%。其中,65岁及以上患者30例,占严重ADR/AE患者总数的40.00%。ADR/AE患者年龄主要集中在45 - 64岁,共1346例,占ADR/AE患者总数的48.14%。所有ADR/AE病例及严重ADR/AE病例均口服仙灵骨葆胶囊/片。女性分别占52.50%和76.00%,女性比例显著高于男性。有ADR/AE病史的患者中,严重ADR/AE高于平均水平,约占1.33%。所有ADR/AE病例及严重ADR/AE病例中,口服仙灵骨葆胶囊/片1 - 3片的比例分别为95.32%和96.00%,符合说明书用法用量。所有ADR/AE病例及严重ADR/AE病例中,每日口服仙灵骨葆胶囊/片2次的比例最高,分别为77.00%和61.00%。严重ADR/AE病例口服仙灵骨葆胶囊/片的用药频次比例略高于所有ADR/AE病例,不符合说明书用法用量。口服仙灵骨葆胶囊的ADR/AE症状表现多样,前10位症状为恶心、皮疹、瘙痒、胃肠功能紊乱、呕吐、腹痛、头晕、腹泻、过敏反应、反流性烧心。口服仙灵骨葆胶囊后严重ADR/AE症状多样,前10位症状为肝功能异常、皮疹、窒息、瘙痒、头晕、呕吐、过敏反应、腹痛、乏力、抽搐。肝功能异常占44.1

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