Term
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Definition
Prednisone (Deltasone®)
Triamcinolone (Kenacort®)
Methylprednisolone (Solu-Medrol®)
MOA: Inhibits prastaglandin and leukotriene synthesis, inhibits neutrophil and monocyte superoxide radical generation
AE: Osteoporosis, myopathies, hypertension, gastritis, glucose intolerance, increased susceptibility to infections, skin atrophy, weight gain
Often used as bridge therapy for patients on DMARDS |
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Term
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Definition
Deltasone®
Oral Corticosteroids |
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Term
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Definition
Kenacort®
Intra-articular Corticosteroids |
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Term
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Definition
Solu-Medrol®
Intra-articular Corticosteroids |
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Term
NSAIDS
(Non-steroidal Anti-inflammatory Drugs) |
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Definition
Aspirin
Diclofenac (Voltaren®)
Etodolac (Lodine®)
Ibuprofen (Motrin®, Advil®)
Naproxen (Naprosyn®, Aleve®)
Nabumetone (Relafen®)
Sulindac (Clinoril®)
Tolmentin (Tolectin®) |
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Term
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Definition
MOA: Inhibition of COX-1 and COX-2, inhibition of COX 2 is responsible for the anti-inflammatory effects of NSAIDS
AE: Gastrointestinal effects (dyspepsia, gastric and duodenal ulcers) |
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Term
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Definition
Several Brand Names Available
Dose: 650 mg every 4 hours, Max= 6000 mg
NSAIDS |
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Term
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Definition
Voltaren®
Dose: 75 mg BID, Max= 200 mg
NSAIDS |
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Term
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Definition
Lodine®
Dose: 300 mg BID, Max= 1200 mg
NSAIDS |
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Term
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Definition
Advil®, Motrin®
Dose: 400 mg TID, Max= 3200 mg
NSAIDS |
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Term
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Definition
Naprosyn®, Aleve®
Dose: 500 mg BID, Max= 1250 mg
NSAIDS |
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Term
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Definition
Relafen®
Dose: 500 mg BID, Max= 2000 mg
NSAIDS |
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Term
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Definition
Clinoril®
Dose: 150 mg BID, Max= 400 mg
NSAIDS |
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Term
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Definition
Tolectin®
Dose: 400 mg TID, Max= 1800 mg
NSAIDS |
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Term
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Definition
Celebrex®
MOA: Inhibits COX-2
Dose: 100 mg BID, Max= 400 mg
COX-2 Inhibitor
**The other two have been taken off the market** |
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Term
Non-Biological Disease Modifying Anti-Rheumatic Drugs (DMARDS) |
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Definition
Methotrexate (Rheumatrex®)
Hydroxychloroquine (Plaquenil®)
Sulfsalazine (Azulfidine®)
Leflunomide (Arava®)
Gold Salts (Aurolate®)
Azathioprine (Imuran®)
Cyclophosphamide (Cytoxan®)
Cyclosporine (Neoral®)
Auranofin (Ridaura®)
D-penicillamine (Cupirimine®) |
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Term
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Definition
Rheumatrex®
MOA: Immunosupressant, folate antimetabolite/antineoplastic agent, interferes with cell reproduction and induces a suppressive effect on rapidly proliferating cells and secretion of cytokines
Onset: 4-6 weeks
Dose: 7.5-15 mg weekly; increase by 2.5 mg increments every 2-4 weeks until a response is evident
Non-biological DMARD |
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Term
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Definition
Plaquenil®
MOA: Antimalarial, inhibits prostaglandin synthesis
Dose: 200-300 mg BID
Onset: Delayed up to 6 weeks
Therapeutic failure if no response after 6 weeks
Important AE: Blurred vision (Retinopathy)
Non-biological DMARD |
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Term
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Definition
Azulfidine®
MOA: Anti-inflammatory, immunomodulator
Dose: 500 mg BID, may increase to 1 gram BID
Onset: 2-3 months
AE: Lupus-like syndrome
Non-biological DMARD |
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Term
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Definition
Arava®
MOA: Inhibits pyrimidine synthesis, causing a decrease in lymphocyte proliferation, and modulation of inflammation
Dose: After loading dose of 100 mg daily for 3 days, maintenance is 20 mg daily
AE: Hepatotoxicity
Pregnancy: X
Non-biological DMARD |
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Term
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Definition
Aurolate®
Not used frequently
Dose: 6 mg daily or 3 mg BID, if response inadequate after 6 months increase to 9 mg, if response inadequate after 3 months, discontinue
AE: Gold toxicity
Not recommended for use during pregnancy
Non-biological DMARD |
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Term
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Definition
Imuran®
MOA: Immunosupressant
Dose: 50-150 mg daily
Onset: 2-3 months
Used for refractory RA or systemic involvement such as rheumatoid vasculitis
Non-biological DMARD |
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Term
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Definition
Cytoxan®
MOA: Immunosuppressant, suppresses T-cell function
Limited for most severe cases of RA
Long-term use can increase risk of malignancy and infection
Non-biological DMARD |
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Term
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Definition
Neoral®
MOA: Inhibits T-cell activation, inhibits interleukin-2 and interferon gamma
Dose: 2.5 mg/kg/day and may increase to 5 mg/kg/day at 2-4 week intervals
Substrate of 3A4
AE: Nephrotoxicity, excessive hair growth, gingival hyperplasia
Non-biological DMARD |
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Term
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Definition
Ridaura®
Dose: 3-6 mg daily, may increase to 9 mg daily
Onset: 4-6 months
Non-biological DMARD |
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Term
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Definition
Cupirimine®
Dose: 250-750 mg daily
Onset: 3-6 months
Non-biological DMARD |
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Term
Tumor Necrosis Factor-alpha (TNFα) Inhibitors |
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Definition
Etanercept (Enbrel®)
Infliximab (Remicade®)
Adalimumab (Humira®)
Golimumab (Simponi®)
Certolizumab (Cimzia®) |
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Term
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Definition
MOA: TNFα antibodies decrease synovitis and joint erosions in collagen-induced arthritis and when administered after disease onset it allows eroded joints to heal.
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Term
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Definition
Enbrel®
Dose: 25 mg Sub-Q twice a week
For patients that have not adequately responded to Non-biological DMARDS
TNFα Inhibitors (Biological DMARDS) |
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Term
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Definition
Remicade®
Dose: 3 mg/kg IV at weeks 0, 2, and 6 weeks, then every 8 weeks
Chimeric Monoclonal Antibody
TNFα Inhibitors (Biological DMARDS) |
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Term
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Definition
Humira®
Human monoclonal antibody
TNFα Inhibitors (Biological DMARDS) |
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Term
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Definition
Simponi®
Human monoclonal antibody
TNFα Inhibitor (Biological DMARDS)
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Term
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Definition
Cimzia®
Humanized Monoclonal Antibody
TNFα Inhibitor (Biological DMARDS) |
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Term
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Definition
Kineret®
Dose: 100 mg daily Sub-Q
Interleukin (IL)-1 Receptor Antagonist (Biological DMARDS) |
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Term
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Definition
Orencia®
T-Cell Activator Inhibitor (Biological DMARDS) |
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Term
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Definition
Rituxan®
Chimeric Monoclonal Antibody
Anti-CD20 Monoclonal Antibody (Biological DMARDS) |
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Term
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Definition
Actemra®
Humanized Monoclonal Antibody
Interleukin (IL)-6 Inhibitor |
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