High anti-TNF alfa drugs trough levels are not associated with the occurrence of adverse events in patients with inflammatory bowel disease
Author:
Affiliation:
1. Gastroenterology Unit, Department of Internal Medicine, University of Genoa, Genoa, Italy;
2. Gastroenterolgy Unit, Department of Surgery, Oncology and Gastroenterology, University of Padua, Padua, Italy
Publisher
Informa UK Limited
Subject
Gastroenterology
Link
https://www.tandfonline.com/doi/pdf/10.1080/00365521.2019.1666914
Reference25 articles.
1. 3rd European Evidence-based Consensus on the Diagnosis and Management of Crohn’s Disease 2016: Part 1: Diagnosis and Medical Management
2. Review article: loss of response to anti-TNF treatments in Crohn’s disease
3. Loss of Response and Need for Adalimumab Dose Intensification in Crohn's Disease: A Systematic Review
4. Loss of Response and Requirement of Infliximab Dose Intensification in Crohn's Disease: A Review
5. Association Between Serum Concentration of Infliximab and Efficacy in Adult Patients With Ulcerative Colitis
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2. Identifying risk factors of anti‐TNF induced skin lesions and other adverse events in paediatric patients with inflammatory bowel disease;Journal of Pediatric Gastroenterology and Nutrition;2023-12-10
3. Predictors and optimal management of tumor necrosis factor antagonist nonresponse in inflammatory bowel disease: A literature review;World Journal of Gastroenterology;2023-08-07
4. Association of Infliximab and Vedolizumab Trough Levels with Reported Rates of Adverse Events: A Cross-Sectional Study;Journal of Clinical Medicine;2021-09-20
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