Frequency of real-world reported adverse drug reactions in rheumatoid arthritis patients

Author:

Giraud Eline L.1ORCID,Jessurun Naomi T.1ORCID,van Hunsel Florence P.A.M.1ORCID,van Puijenbroek Eugene P.1ORCID,van Tubergen Astrid2ORCID,Ten Klooster Peter M.34ORCID,Vonkeman Harald E.45ORCID

Affiliation:

1. Netherlands Pharmacovigilance Centre Lareb, ‘s-Hertogenbosch, The Netherlands

2. Department of Medicine, Division of Rheumatology, Maastricht University Medical Center, Maastricht, the Netherlands and Care and Public Health Research Institute (CAPHRI), Maastricht University, Maastricht, The Netherlands

3. Transparency in Healthcare B.v., Hengelo, The Netherlands

4. Department of Psychology, Health & Technology, University of Twente, Enschede, The Netherlands

5. Department of Rheumatology and Clinical Immunology, Medisch Spectrum Twente, Enschede, The Netherlands

Funder

No sources of funding

Publisher

Informa UK Limited

Subject

Pharmacology (medical),General Medicine

Reference39 articles.

1. Rheumatoid arthritis: pathological mechanisms and modern pharmacologic therapies

2. EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2013 update

3. Managing the drug treatment of rheumatoid arthritis

4. Guideline A. On Summary Of Product Characteristics (SmPC). 2009. (Directorate-General ECEAI, editor). p. 29.

5. DREAM-RA registry. 2020. [cited 2020 May 1]. Available from: https://www.dreamregistry.nl

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