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dc.contributor.authorBilgici A.
dc.contributor.authorKuru Ö.
dc.date.accessioned2020-06-21T09:14:44Z
dc.date.available2020-06-21T09:14:44Z
dc.date.issued2003
dc.identifier.issn1300-0691
dc.identifier.urihttps://hdl.handle.net/20.500.12712/2497
dc.description.abstractArresting and preventing structural damage is a primary goal of therapy in rheumatoid arthritis(RA). The current trent in the treatment of RA is to intervene early, before the development of irreversible joint damage. The majority of patients with newly diagnosed RA should be started on disease-modifying antirheumatic drug (DMARD) therapy within 3 months of diagnosis. Each DMARD has specific toxicity that requires careful monitoring. Therefore, physician who care for these patients need to be aware of the potential adverse effects of these medications. The physician should also assess many factors such as compliance of patient, the severity and prognosis of the disease, and the physician's own confidence in administering the drug for the decision regarding the initiation and selection of a DMARD.en_US
dc.language.isoturen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDrug therapyen_US
dc.subjectDrug toxicityen_US
dc.subjectEarly rheumatoid artritisen_US
dc.subjectRheumatoid artritisen_US
dc.titleEarly therapy in active rheumatoid arthritisen_US
dc.title.alternativeAkti?f romatoi?d artri?tte erken tedavi?en_US
dc.typereviewen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume14en_US
dc.identifier.issue1en_US
dc.identifier.startpage37en_US
dc.identifier.endpage47en_US
dc.relation.journalJournal of Rheumatology and Medical Rehabilitationen_US
dc.relation.publicationcategoryDiğeren_US


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