Cargando…

Cardiotoxicity in Biological Agent-Targeted Therapy for Rheumatoid Arthritis: ADR Signal Mining and Analysis of Food and Drug Administration Adverse Event Reporting System Database

Purpose: Biologic agent-induced cardiotoxicity is markedly concerning. Rheumatoid arthritis (RA) treated with biologic agents is known to have the potential for cardiotoxicity; however, existing clinical evidence is not adequate to explain real-world patterns of cardiotoxicity. In this study, we qua...

Descripción completa

Detalles Bibliográficos
Autores principales:	Tang, Xiaoyan, Xu, Xiaolin, Li, Ji, Zhao, Bin
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Pediatrics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546333/ https://www.ncbi.nlm.nih.gov/pubmed/34712629 http://dx.doi.org/10.3389/fped.2021.716648

Ejemplares similares

A web resource for mining HLA associations with adverse drug reactions: HLA-ADR
por: Ghattaoraya, Gurpreet S., et al.
Publicado: (2016)

Children and ADRs (Adverse Drug Reactions)
por: Napoleone, Ettore
Publicado: (2010)

Drug‐target‐ADR Network and Possible Implications of Structural Variants in Adverse Events
por: Dafniet, Bryan, et al.
Publicado: (2020)

Medical students as junior adverse drug event managers facilitating reporting of ADRs
por: Reumerman, Michael O., et al.
Publicado: (2021)

Adverse Events of DOACs in Children
por: Bosch, Alessandra, et al.
Publicado: (2022)

Placebo-Related Adverse Events in Rheumatoid Arthritis
por: Sharma, Ratna Shree, et al.
Publicado: (2022)

Analysis of anticholinergic adverse effects using two large databases: The US Food and Drug Administration Adverse Event Reporting System database and the Japanese Adverse Drug Event Report database
por: Nagai, Junko, et al.
Publicado: (2021)

Epidermiology of adverse drug reactions (ADRs) in the elderly
por: Ju-Young, Kim, et al.
Publicado: (2014)

Adverse Drug Reactions (ADRs) of Montelukast in Children
por: Al-Shamrani, Abdullah, et al.
Publicado: (2022)

ADReCS: an ontology database for aiding standardization and hierarchical classification of adverse drug reaction terms
por: Cai, Mei-Chun, et al.
Publicado: (2014)

Spontaneous Reporting on Adverse Events by Consumers in the United States: An Analysis of the Food and Drug Administration Adverse Event Reporting System Database
por: Toki, Tadashi, et al.
Publicado: (2018)

Network Characteristic Analysis of ADR-related Proteins and Identification of ADR-ADR Associations
por: Chen, Xiujie, et al.
Publicado: (2013)

Patterns of adverse drug reactions (ADRs) in Saudi Arabia
por: Bin Yousef, Nora, et al.
Publicado: (2022)

Administrative Data Research Northern Ireland (ADR NI)
por: O’Reilly, D, et al.
Publicado: (2020)

Safety signals of albumin-bound paclitaxel: Data mining of the Food and Drug Administration adverse event reporting system
por: Wang, Yuwei, et al.
Publicado: (2023)

Adverse Events in Patients With Rheumatoid Arthritis and Psoriatic Arthritis Receiving Long-Term Biological Agents in a Real-Life Setting
por: de Camargo, Mayara Costa, et al.
Publicado: (2019)

Risk of Major Adverse Cardiovascular Events in Patients With Rheumatoid Arthritis
por: Mal, Kheraj, et al.
Publicado: (2020)

Detecting associations between behavioral addictions and dopamine agonists in the Food & Drug Administration’s Adverse Event database
por: Gendreau, Katherine E., et al.
Publicado: (2014)

The use of administrative health care databases to identify patients with rheumatoid arthritis
por: Hanly, John G, et al.
Publicado: (2015)

Brief Report: The Genetic Profile of Rheumatoid Factor–Positive Polyarticular Juvenile Idiopathic Arthritis Resembles That of Adult Rheumatoid Arthritis
por: Hinks, Anne, et al.
Publicado: (2018)

iADRs: towards online adverse drug reaction analysis
por: Lin, Wen-Yang, et al.
Publicado: (2012)

Assessment of left heart dysfunction to predict doxorubicin cardiotoxicity in children with lymphoma
por: Chen, Jiaqi, et al.
Publicado: (2023)

Adverse reaction profiles of hemorrhagic adverse reactions caused by direct oral anticoagulants analyzed using the Food and Drug Administration Adverse Event Reporting System (FAERS) database and the Japanese Adverse Drug Event Report (JADER) database
por: Shimada, Kazuyo, et al.
Publicado: (2019)

Cardiotoxicity After Anthracycline Chemotherapy for Childhood Cancer in a Multiethnic Asian Population
por: Tan, Varen Zhi Zheng, et al.
Publicado: (2021)

Adverse Events and Unsuccessful Intubation Attempts Are Frequent During Neonatal Nasotracheal Intubations
por: Tippmann, Susanne, et al.
Publicado: (2021)

Effects of pharmacogenetic profiles on pediatric pain relief and adverse events with ibuprofen and oxycodone
por: Ali, Samina, et al.
Publicado: (2023)

Validation of algorithms for selecting rheumatoid arthritis patients in the Tuscan healthcare administrative databases
por: Convertino, Irma, et al.
Publicado: (2021)

Adverse Events During Supervised Exercise Interventions in Pediatric Oncology—A Nationwide Survey
por: Gauß, Gabriele, et al.
Publicado: (2021)

Machine Learning-Based Systems for the Anticipation of Adverse Events After Pediatric Cardiac Surgery
por: Garcia-Canadilla, Patricia, et al.
Publicado: (2022)

Systematic analysis of safety profile for darunavir and its boosted agents using data mining in the FDA Adverse Event Reporting System database
por: Tian, Xiaojiang, et al.
Publicado: (2021)

Adverse Drug Reactions, Power, Harm Reduction, Regulation and the ADRe Profiles
por: Jordan, Sue, et al.
Publicado: (2018)

Conservative Management of Low Back Pain and Scoliosis in a Patient With Rheumatoid Arthritis: Eight Years Follow-Up
por: Chu, Eric Chun-Pu, et al.
Publicado: (2023)

Lung Cancer Adverse Events Reports for Angiotensin-Converting Enzyme Inhibitors: Data Mining of the FDA Adverse Event Reporting System Database
por: Meng, Long, et al.
Publicado: (2021)

Investigating ADR mechanisms with Explainable AI: a feasibility study with knowledge graph mining
por: Bresso, Emmanuel, et al.
Publicado: (2021)

Adverse Drug Reactions (ADR) in the inPatients of Medicine Department of a Rural Tertiary Care Teaching Hospital and Influence of Pharmacovigilance in Reporting ADR
por: Gor, A.P., et al.
Publicado: (2008)

Safety Profile of Levonorgestrel: A Disproportionality Analysis of Food and Drug Administration Adverse Event Reporting System (Faers) Database
por: Kurian, Anitha, et al.
Publicado: (2018)

Hepatic failure associated with immune checkpoint inhibitors: An analysis of the Food and Drug Administration Adverse Event Reporting System database
por: Xu, Ye, et al.
Publicado: (2023)

Inferring disease severity in rheumatoid arthritis using predictive modeling in administrative claims databases
por: Chandran, Urmila, et al.
Publicado: (2019)

Mining Disease Risk Patterns from Nationwide Clinical Databases for the Assessment of Early Rheumatoid Arthritis Risk
por: Chin, Chu Yu, et al.
Publicado: (2015)

The pediatric oncology exercise field speeds up to address important issues regarding chemotherapy-related cardiotoxicity
por: Caru, Maxime, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_kfh6cl1r3v3nccat9hmt9ccvm0