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Export This article provides an overview of current results from the German biologics register RABBIT on the safety of biologic and targeted synthetic disease-modifying antirheumatic drugs in rheumatoid arthritis. Collaborative data from the European biologics registries show no evidence for an overall increased risk of malignancy with TNF inhibitors. Venous thromboembolism occurs less frequently under TNF inhibitors than under conventional synthetic DMARDs. Regarding interleukin-6 inhibitors, the incidence of lower intestinal tract perforations is increased with tocilizumab and presents with atypical symptoms. There is no evidence of increased facial paresis with tocilizumab. Janus kinase inhibitors increase the risk for the occurrence of herpes zoster. New data on biosimilars suggest that they can be used with a comparable safety profile to originator drugs.
SEEK ID: https://ldh.drfz.imise.uni-leipzig.de/publications/83
DOI: 10.1055/a-1334-7609
Projects: RABBIT (Rheumatoid Arthritis - Observation of Biologic Therapies)
Publication type: Journal
Journal: Dtsch Med Wochenschr
Citation: Dtsch Med Wochenschr 146(15):998-1002
Date Published: 2021
URL: https://www.ncbi.nlm.nih.gov/pubmed/34344036
Registered Mode: imported from a bibtex file
SubmitterViews: 43
Created: 15th Jul 2025 at 09:46
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https://orcid.org/0000-0002-3372-2021