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浏览/检索结果: 共5条，第1-5条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 A Survey of the FDA's Adverse Event Reporting System Database Concerning Urogenital Tract Infections and Sodium Glucose Cotransporter-2Inhibitor Use 期刊论文 2019, 卷号: 10, 期号: 3, 页码: 1043-1050 作者:  Shen, Juan;  Yang, Jincheng;  Zhao, Bin 收藏  |  浏览/下载：8/0  |  提交时间：2020/01/03 Adverse drug reactions  FAERS  Sodium glucose cotransporter-2 inhibitors  Urogenital tract infections   Association between Concomitant Use of Acyclovir or Valacyclovir with NSAIDs and an Increased Risk of Acute Kidney Injury: Data Mining of FDA Adverse Event Reporting System 期刊论文 BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2018, 卷号: 41, 期号: 2, 页码: 158-162 作者:  Yue, Zhihua[1];  Shi, Jinhai[2];  Li, Haona[3];  Li, Huiyi[4] 收藏  |  浏览/下载：5/0  |  提交时间：2019/12/23 acyclovir  valacyclovir  nonsteroidal anti-inflammatory drug (NSAID)  acute kidney injury  data mining  FDA Adverse Event Reporting System (FAERS)   Proton Pump Inhibitors and the Risk for Fracture at Specific Sites: Data Mining of the FDA Adverse Event Reporting System 期刊论文 SCIENTIFIC REPORTS, 2017, 卷号: 7 作者:  Han, Zhengqi;  Wang, Xueju;  Atkinson, Elizabeth J.;  Liu, Hongfang;  Amin, Shreyasee 收藏  |  浏览/下载：2/0  |  提交时间：2019/12/05 Digoxin-induced anemia among patients with atrial fibrillation and heart failure: clinical data analysis and drug-gene interaction network 期刊论文 ONCOTARGET, 2017, 卷号: 8, 页码: 57003-57011 作者:  Lin, Yubi[1,2,3];  He, Siqi[1,2,3];  Feng, Ruiling[1,2,3];  Xu, Zhe[4];  Chen, Wanqun[5] 收藏  |  浏览/下载：4/0  |  提交时间：2019/04/24 digoxin  atrial fibrillation  heart failure  anemia  FDA adverse event reporting system   Opportunities for Web-based Drug Repositioning: Searching for Potential Antihypertensive Agents with Hypotension Adverse Events 期刊论文 JOURNAL OF MEDICAL INTERNET RESEARCH, 2016, 卷号: 18 作者:  Wang, Kejian;  Wan, Mei;  Wang, Rui-Sheng;  Weng, Zuquan 收藏  |  浏览/下载：4/0  |  提交时间：2019/11/21 hypotension  FAERS  big data  Web-based drug repositioning  openFDA  FDA Adverse Event Reporting System  antihypertensive drugs