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Pharmacotherapy Options in Rheumatoid Arthritis
Author(s) -
Pradeep Kumar,
Snehashish Banik
Publication year - 2013
Publication title -
clinical medicine insights arthritis and musculoskeletal disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.418
H-Index - 21
ISSN - 1179-5441
DOI - 10.4137/cmamd.s5558
Subject(s) - abatacept , medicine , tofacitinib , tocilizumab , leflunomide , sulfasalazine , rheumatoid arthritis , rituximab , hydroxychloroquine , infliximab , etanercept , methotrexate , pharmacotherapy , antirheumatic agents , intensive care medicine , antirheumatic drugs , adalimumab , pharmacology , disease , covid-19 , lymphoma , ulcerative colitis , infectious disease (medical specialty)
Drugs form the mainstay of therapy in rheumatoid arthritis (RA). Five main classes of drugs are currently used: analgesics, non-steroidal anti-inflammatories (NSAIDs), glucocorticoids, nonbiologic and biologic disease-modifying antirheumatic drugs. Current clinical practice guidelines recommend that clinicians start biologic agents if patients have suboptimal response or intolerant to one or two traditional disease modifying agents (DMARDs). Methotrexate, sulfasalazine, leflunomide and hydroxychloroquine are the commonly used DMARDs. Currently, anti-TNF is the commonly used first line biologic worldwide followed by abatacept and it is usually combined with MTX. There is some evidence that tocilizumab is the most effective biologic as a monotherapy agent. Rituximab is generally not used as a first line biologic therapy due to safety issues but still as effective as anti-TNF. The long term data for the newer oral small molecule biologics such as tofacitinib is not available and hence used only as a last resort.

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