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Questions and Answers
Which drug is a prodrug and inhibits T-cell proliferation?
Which targeted synthetic DMARD is administered orally and indicated for rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, polyarticular juvenile idiopathic arthritis, and ulcerative colitis?
Which drug is a folate antagonist and is considered first-line for rheumatoid arthritis?
Which drug should be reserved for severe, progressive rheumatoid arthritis that has not responded to safer DMARDs?
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Which drug carries a black box warning for fatal toxicities of the bone marrow, liver, lungs, and kidneys?
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Which drug is indicated for IV therapy of adults with moderate to severe RA who have not responded to one or more TNF inhibitors?
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Which targeted synthetic DMARD carries a black box warning for serious or fatal infection risk, heart-related events, cancer, and blood clots?
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Which conventional DMARD has side effects including nausea, hair loss, mouth ulcers, and hepatoxicity?
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Which drug is considered a last choice and is used for rejection of transplanted organs?
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Which drug is associated with the need for G6PD testing, baseline eye exam, and routine eye screens due to potential toxic retinopathy?
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Which type of drugs are biologic DMARDs?
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What is the risk associated with all biologic DMARDs?
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How are biologic DMARDs manufactured?
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What is a type of biologic DMARD?
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What is the MOA of adalimumab (Humira)?
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What is the MOA of rituximab (Rituxan)?
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What is the MOA of abatacept (Orencia)?
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For which condition is adalimumab (Humira) indicated?
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What is the target of rituximab (Rituxan)?
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What is the common risk associated with all biologic DMARDs?
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Biologic DMARDs are not immunosuppressive drugs.
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Biologic DMARDs are usually combined with methotrexate.
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MAbs are proteins derived only from human sources.
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Adalimumab is indicated for mild rheumatoid arthritis.
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Rituximab binds to and neutralizes tumor necrosis factor (TNF).
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Rituximab is indicated for moderate to severe rheumatoid arthritis.
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Abatacept is a T-cell activation inhibitor.
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Interleukin antagonists are used in the treatment of moderate to severe RA.
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All biologic DMARDs pose a risk for serious infections and perhaps cancer.
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Abatacept is the only drug in its class.
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Rheumatoid arthritis is not listed as an indication for tofacitinib (Xeljanz).
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Sulfasalazine (Azulfidine) is a first-line drug for rheumatoid arthritis.
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Leflunomide (Arava) is not indicated for systemic lupus erythematosus (SLE) or malaria.
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Cyclosporine (Gengraf) does not require G6PD testing.
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Tofacitinib (Xeljanz) carries a black box warning for serious or fatal infection risk, heart-related events, cancer, and blood clots.
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Biologic DMARDs tend to have a delayed onset of 3-6 months for full therapeutic effect.
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Methotrexate (Rheumatrex, Trexall) is indicated for the treatment of rheumatoid arthritis, psoriasis, juvenile idiopathic arthritis (JIA), and oncology.
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Rituximab + methotrexate is indicated for subcutaneous therapy of adults with moderate to severe rheumatoid arthritis who have not responded to one or more TNF inhibitors.
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Baricitinib (Olumiant) has a 16% risk of patients developing infection.
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NSAIDs such as aspirin and celecoxib are not used in the management of gout.
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