Arama Sonuçları - "Food and Drug Administration"

Analysis of Adverse Events and Medical Errors in Long-Term Hormone Treatments for Endometriosis: A Study Based on the US Food and Drug Administration Event Reporting System Yazar: Zhang Y, Zhu Y, Sun J

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Analysis of acute pancreatitis associated with SGLT-2 inhibitors and predictive factors of the death risk: Based on food and drug administration adverse event report system database Yazar: Lin Zhang, Wei Mao, Xingxing Li, Xiaowen Wang, Jifang Liu, Sang Hu, Jing Hu

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A pharmacovigilance study of chronic kidney disease in diabetes mellitus patients with statin treatment by using the US Food and Drug Administration adverse event reporting system Yazar: Jingyi Zhang, Yuting Guo, Chunyan Wei, Yu Yan, Yu Yan, Huifang Shan, Bin Wu, Bin Wu, Fengbo Wu

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Progressive multifocal leukoencephalopathy reports in rheumatoid arthritis concerning different treatment patterns-an exploratory assessment using the food and drug administration adverse event reporting system Yazar: Takeshi Honma, Kenji Onda, Koichi Masuyama

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The Food and Drug Administration Biologics Effectiveness and Safety Initiative Facilitates Detection of Vaccine Administrations From Unstructured Data in Medical Records Through Natural Language Processing Yazar: Matthew Deady, Hussein Ezzeldin, Kerry Cook, Douglas Billings, Jeno Pizarro, Amalia A. Plotogea, Patrick Saunders-Hastings, Artur Belov, Barbee I. Whitaker, Steven A. Anderson

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Trust but Verify: Lessons Learned for the Application of AI to Case-Based Clinical Decision-Making From Postmarketing Drug Safety Assessment at the US Food and Drug Administration Yazar: Robert Ball, Andrew H Talal, Oanh Dang, Monica Muñoz, Marianthi Markatou

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Common Immune-Related Adverse Events of Immune Checkpoint Inhibitors in the Gastrointestinal System: A Study Based on the US Food and Drug Administration Adverse Event Reporting System Yazar: Xiaoyin Bai, Shiyu Jiang, Yangzhong Zhou, Hongnan Zhen, Junyi Ji, Yi Li, Gechong Ruan, Yang Yang, Kaini Shen, Luo Wang, Guanqiao Li, Hong Yang

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An evaluation of adverse drug reactions and outcomes attributed to kratom in the US Food and Drug Administration Adverse Event Reporting System from January 2004 through September 2021 Yazar: Xiaotong Li, Patrick Ndungu, Sanya B. Taneja, Maryann R. Chapin, Susan B. Egbert, Krishi Akenapalli, Mary F. Paine, Sandra L. Kane‐Gill, Richard D. Boyce

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The Future of Medical Device Regulation Innovation and Protection

Konular: “…food and drug administration…”
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Unrecognized maternal heart rate artefact in cases of perinatal mortality reported to the United States Food and Drug Administration from 2009 to 2019: a critical patient safety issue Yazar: Daniel J. Kiely, Lawrence W. Oppenheimer, James C. Dornan

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Adverse event reporting of the IGF-1R monoclonal antibody teprotumumab: a real-world study based on the US food and drug administration adverse event reporting system Yazar: Jiawei Zhao, Yong Tao

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A real-world study of antifibrotic drugs-related adverse events based on the United States food and drug administration adverse event reporting system and VigiAccess databases Yazar: Menglin He, Taoran Yang, Jian Zhou, Rurong Wang, Xuehan Li

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Reflexões sobre o impacto causado pelo alerta do Food and Drug Administration (FDA) americano sobre o morcelamento eletromecânico uterino e/ou de miomas Yazar: Luiz Gustavo Oliveira Brito, Júlio César Rosa e Silva, Antonio Alberto Nogueira

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Agranulocytosis and secondary infection related to JAK inhibitors and IL-6 receptor blockers: a disproportionality analysis using the US Food and drug administration adverse event reporting system Yazar: Chunyan Wei, Wanhong Yin, Wanhong Yin, Tingting Hu, Jingyi Zhang, Huifang Dan, Bin Wu

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Real-world study of adverse events associated with gepant use in migraine treatment based on the VigiAccess and U.S. Food and Drug Administration's adverse event reporting system databases Yazar: Qiaofang Liang, Xiaolin Liao, Hongwen Wu, Yushen Huang, Taolin Liang, Hailong Li, Hailong Li, Hailong Li

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A decade comparison of regulatory decision patterns for oncology products to all other non‐oncology products among Swissmedic, European Medicines Agency, and US Food and Drug Administration Yazar: Ulrich‐P. Rohr, Mario Iovino, Leonie Rudofsky, Qiyu Li, Stephanie Juritz, Arunas Gircys, Oliver Wildner, Magda Bujar, Claus Bolte, Simon Dalla Torre di Sanguinetto, Anita Wolfer

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Potential safety signal of pregnancy loss with vascular endothelial growth factor inhibitor intraocular injection: A disproportionality analysis using the Food and Drug Administration Adverse Event Reporting System Yazar: Takamasa Sakai, Chiyo Mori, Chiyo Mori, Fumiko Ohtsu

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Examining worldwide postmarketing suicides from biologics used for psoriasis with a focus on brodalumab: A cross-sectional analysis using the Food and Drug Administration Adverse Event Reporting System (FAERS) Yazar: Samuel Yeroushalmi, BS, Mimi Chung, BA, Erin Bartholomew, BA, Marwa Hakimi, MD, John Koo, MD

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A systematic review of Ebola virus disease outbreaks and an analysis of the efficacy and safety of newer drugs approved for the treatment of Ebola virus disease by the US Food and Drug Administration from 2016 to 2020 Yazar: Palanisamy Sivanandy, Pee Hui Jun, Lai Weng Man, Ng Sin Wei, Nicole Foo Kar Mun, Celestine Ang Jia Yii, Charissa Cheah Xiao Ying

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The Risk and Clinical Implications of Antibiotic-Associated Acute Kidney Injury: A Review of the Clinical Data for Agents with Signals from the Food and Drug Administration's Adverse Event Reporting System (FAERS) Database Yazar: Kalin M. Clifford, Ashley R. Selby, Kelly R. Reveles, Chengwen Teng, Ronald G. Hall, Jamie McCarrell, Carlos A. Alvarez

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