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pharmacology of DMARD's

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Answer
methotrexate   mechanism of action probably relates to secondary effects of polymorphonuclear chemotaxis secondary to inhibition of aminoimidazolecarboxamide transformylase and thimidylate synthase inhibition  
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methotrexate   decreases the rate of appearance of new erosions in RA, evidence supports its use in juvenile chronic arthritis, polymyositis, wegner's, SLE, and vasculitits  
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methotrexate   side effects: nausea and mucosal ulcers are the most common side effects. progressive dose related hepatoxicity occurs frequently  
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chlorambucil   cross-links DNA, therby preventing cell replication.  
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chlorambucil   most common toxicity is dose realted bone marrow supression. infertility with azoospermia and amenorrhea also occurs. the risk of neoplasia is increased with the relative risk of leukemia increased about 10 fold after more than 3 years of use  
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cyclophosphamide   cross links DNA to prevent cell replication  
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cyclophosphamide   causes significant dose related inferility in men and women as well as bone marrow suppression, alopecia, hemorrhagic cystitis, and rarely bladder carcinoma  
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cyclosporine   regulates gene transcription to inhibit IL1 and IL@ receptor production and secondarily inhibits macrophage T cell interaction and T cell response  
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cyclosporine   grapefruit juice increaes its bioavailability up to 60%  
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cyclosporine   has significant nephrotoxicity, and its toxicity can be increased by drug interactions with diltiazem, K sparing diuretics, and other drugs inhibiting CYP3A  
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azathioprine   suppresses inosinic acid synthesis, B cell and T cell function, immunoglobulin production, and IL-2 secretion by 6-Thioguanine which is the major merabolite  
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azathioprine   toxicity includes bone marrow suppression, gastrointestinal disturbances and some increase in infection risk  
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mycophenolate mofetil   inhibits cytosine monophosphate dehydrogenase and secondarily inhibits T cell lymophocyte proliferation  
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mycophenolate mofetil   effective for the treatment of renal disease due to systemic lupus erythematosus and may be useful in vasculitis and Wegener's granulomatosis  
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mycophenolate mofetil   side effects similar to azathioprine with a possibly decreased incidence of fungal infections  
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Gold   alters the morphology and functional capabilities of macrophages  
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Gold   IM compounds also alter lysosomal enzyme activity, reduce histamine release from mast cells, inactivates the first componant of complement and suppresses the phagocytic activitys of PMN's  
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Gold   tends to concentrate in synovial membranes, liver, kidney, spleen, lymph nodes and bone marrow after IM administration  
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Gold   adverse effects: pruitic skin rash sometimes associated with eosinophilia. stomatitis and a metallic taste in the mouth are common. hematologic abnormalities may occur  
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sulfasalazine   IgA and IgM rheumatoid factor production are decreased  
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sulfaslazine   adverse effects incluse nausea, vomiting headache, and rash. hemolytic anemia and methemoglobinemia also accur but rarely. reversible infertility occurs in men.  
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adalimumab   anti TNF monoclonal antibody; down regulates macrophage and T cell function  
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adalimumab   has a half life of 9-14 days  
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adalimumab   can reactivate latent TB. anti-dsDNA and anti ANA has been documented  
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inflixamib   adverse reactions: URI, nausea, headache, sinusitis, rash, and cough are common. can reactivate latent TB  
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