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Merck

Update 2011: leflunomide in rheumatoid arthritis - strengths and weaknesses.

Current opinion in rheumatology (2011-03-24)
Frank Behrens, Michaela Koehm, Harald Burkhardt
ABSTRAKT

Leflunomide is often used as a first choice disease-modifying antirheumatic drug after methotrexate. New data are available for efficacy and safety in both, monotherapy and combination with biologicals. New data on efficacy demonstrate comparable effect sizes for leflunomide and methotrexate in the treatment of signs and symptoms in combination with tumour necrosis factor-blocking agents and rituximab. Equipotency has also been demonstrated by a recent radiographic outcome study on methotrexate and leflunomide monotherapy. Pharmacogenetic studies indicate an impact of polymorphisms on the variability in serum levels of the compound with potential relevance to effectiveness and tolerability in individual patients. Genetic factors are also likely to contribute to the significantly increased risk for leflunomide-induced pulmonary disease reported in Asia. Because pre-existing interstitial lung disease as well as methotrexate-induced pneumonitis have been identified as risk factors for leflunomide-induced pulmonary disease, the use of leflunomide as an alternative to methotrexate is limited under these conditions. Effectiveness of leflunomide renders it a potent treatment option in rheumatoid arthritis. The known tolerability issues resulting in a less favourable adherence to therapy constitutes a weakness. However, documented data from large registries indicate that leflunomide is safe as far as the contraindications and recommendations for monitoring are regarded.

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Leflunomide, European Pharmacopoeia (EP) Reference Standard
Leflunomide for peak identification, European Pharmacopoeia (EP) Reference Standard
USP
Leflunomide, United States Pharmacopeia (USP) Reference Standard
Sigma-Aldrich
Leflunomide, Immunosuppressant
Supelco
Leflunomide, Pharmaceutical Secondary Standard; Certified Reference Material