RISE registry reveals potential gaps in medication safety for new users of biologics and targeted synthetic DMARDs

Author:

Schmajuk GabrielaORCID,Li Jing,Evans Michael,Anastasiou ChristineORCID,Izadi Zara,Kay Julia L.,Hammam Nevin,Yazdany Jinoos

Funder

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Agency for Healthcare Research and Quality

Publisher

Elsevier BV

Subject

Anesthesiology and Pain Medicine,Rheumatology

Reference23 articles.

1. 2012 update of the 2008 American college of rheumatology recommendations for the use of disease modifying antirheumatic drugs and biologic agents in the treatment of rheumatoid arthritis;Singh;Arthritis Care Res,2012

2. Preventing hepatitis b reactivation due to immunosuppressive drug treatments;Perrillo;JAMA,2015

3. Tuberculosis associated with blocking agents against tumor necrosis factor-alpha–California, 2002-2003;MMWR Morb Mortal Wkly Rep,2004

4. Gaps in ambulatory patient safety for immunosuppressive specialty medications;Patterson;Jt Comm J Qual Patient Saf,2019

5. Using health-system-wide data to understand hepatitis B virus prophylaxis and reactivation outcomes in patients receiving rituximab;Schmajuk;Medicine (Baltimore),2017

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