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12 Cards in this Set

  • Front
  • Back
Arava (Leflunomide)

MOA
Indication
Dose
Side effects
Black box warning
Immunosuppresion
Skin rxn
Drug elimination recommended?
MOA: leflunomide is an immunodulatory agent that inhibits pyrimidine synthesis, resulting in antiproliferative and anti-inflammatory effects. Leflunomide is a prodrug. For CMV it may interfere w virion assembly

Indication - rheumatoid arthritis; indicated to reduce signs and symptoms, and to inhibit structural damage and IMPROVE PHYSICAL FUNCTION

Dose - 100mg q d x 3 days; then 20 mg thereafter

Side effects:
Hepatotoxicity - initial monthly LFTs; d/c if AST 3x ULN

BBW: not for women of child bearing age

Immunosuppresion: check wbc, platelet, Hb, hematocrit monthly

Skin rxn; SJS is a posibility

Drug elimination recs. Use chlolestyramine 8 grams tid x 11 days to help increase leflunomide excretion
Rheumatrex, Trexall (Methotrexate)

MOA
Indication
Dose
Side effects
Black Box Warning
Monitoring
Therapeutic response
Any supplements?
Overdose
MOA: folate antimetabolit that inhibits DNA synthesis, Methotrexate irreversibly binds to DIHYDROFOLATE REDUCTASE, and THYMIDYLATE SYNTHASE, resulting in inhibition of purine and thymidylic acid synthesis.

*Methotrexate is cell cycle specific for S PHASE

Indication
DOC for psoriatic arthritis
rheumatoid arthritis

Dose: 10-25 mg q wk

Side effects: ulcerative stomatitis, leukopenia, nausea, abdominal distress, malaise, fatigue, chills, fever, dizziness, alopecia

Black Box Warning
Can be fatal - monitor for bone marrow, liver, lung and kidney toxicities. Hepatotoiicity, fibrosis and cirrhosis after prolonged use

Monitor hematology monthly, LFTs and renal fnx q 1-2 months.

Therapeutic Response
3-6 weeks

Overdose
Use leucovorin

Can Supplement with Folic acid
Cuprimine (Penicillamine)

MOA
Indication
Dose
Side effects
MOA: chelates with lead, copper, mercury and other heavy metals to form stable, soluble complexes that are excreted in urine; depresses circulating IgM rheumatoid factor, depresses Tcell but not Bcell activity, combines with cystine to form a compound which is more soluble, thus systine calculi are prevented

Dose 125 or 250 mg/day; increase at 1-3 months

*MAX 1.5 gm/day

Indication
Wilson's Disease - copper tox
ACTIVE RA
Cystinuria

Cystinuria - inherited autosomal recessive disorder, characterized by formation of cystine stones in kidneys, ureter, and bladder

Rheumatoid Arthritis - may take 2-3 months before therapeutic activity - sort of last line - restrict to pts with sever, active disease and failed to respond to conventional therapy

Side effects
Hematological - can be severe - CBC wtih Diff, HB, platelet counts q 2 wks

Hematuria up to 15%
Plaquenil (hydroxychloroquine)

MOA
Indication
Not for use in...
Dose
Side effects
Who are incredible sensitive to plaquenil?
MOA: interferes with digestive vacuole fxn within sensitive malarial parasites by increasing the pH and interfering with lysosomal degradation of hemoglobin; inhibits locomotion of neutrophils and chemotaxis of eosinophils; impairs comlement-dependent antigen-antibody rxns

Indication:
Suppression and treatment of acute attacks of malaria; treatment of systemic lupus erythematosus (SLE) and RHEUMATOID ARTHRITIS

NOT for use in Psoriatic Arthritis - can cause rash

Dose - 400-600mg q d (good response after 4-12 wks)

Side effects - Retinopathy

**CHILDREN are extremely sensitive to plaquenil...DO NOT GIVE TO CHILDREN
Aralen (Chloroquine)

Indication
Used off label for RA

Indicated for malaria and extraintestinal amebiasis
Solganal (Aurothioglucose)

MOA
Dose/Adminstration
GOLD SALT

MOA: gold inhibits the release of HMGB1 by interfering with interferon beta and nitric oxide. HMGB1 (high mobility group box 1) is an abundant chromatin protein that acts as a cytokine

Dose: 50 mg deep IM weekly; START with 10mg first week; 25mg second week; 50 mg first week
Ridaura (Auranofin)

MOA
Dose/Administration
GOLD SALT

MOA: gold inhibits the release of HMGB1 by interfering with interferon beta and nitric oxide. HMGB1 (high mobility group box 1) is an abundant chromatin protein that acts as a cytokine

Dose:
ONLY PO GOLD SALT
3mg bid, increase to tid after 6 months
Sandimmune, Neoral (cyclosporin)

MOA
Indication
Dose
Side effects
Blackbox Warning
Labs before treatment
Do not give what when taking?
MOA: Inhibition of production and release of interleukin II and inhibits interleukin II-induced activation of resting T-lymphocytes

Indication
Sandimmune; prophylaxis of organ rejection in kidney, liver, heart allogeneic transplants. Always used with adrenal corticosteroids

Neoral
RA

Dose:
Neoral for RA - 1.25mg/kg/day BID; may increase to 0.5-0.75 mg/kg/day after 8 wks and again after 12 wks

*MAX 4mg/kg/day - stop if no benefit after 16 wks

Decrease dose 25-50% if SCr 30% above baseline

Onset of action usually 4-8 wks

Side effects - renal dysfunction, HTN, HA, GI disturbances, hirsutism/hypertrichosis

Blackbox - Neoral and Sandimmune are NOT bioequivelant; Neoral has INCREASED bioavailability compared to Sandimmune

Labs before starting: Scr, BP, CBC, LFT

DO NOT TAKE LIVE VACCINES
Azulfindine En-Tabs (Sulfasalazine)

MOA
Indication
Dose
Side effects
Labs
DO NOT USE THIS
MOA: acts locally in the colon to decrease the inflammatory response and systemically interferes with secretion by inhibiting prostaglandin syntesis

Indication:
RA, psoriatic arthritis, Ankylosing spondylitis, ulcerative colitis, chron's disease

Side effects: stomach upset, N/V, diarrhea, reversible oligospermia, may cuase urine to turn ORANGE, reversible when med is stopped

Labs - CBC w diff, LFT before starting, and every 2 weeks for first three months of therapy. Also periodically check renal function

DO NOT USE if allergic to other sulfa medications

Also, use in caution with severe allergy or bronchial asthma

Adequate water must be given to prevent crystalluria and stone formation

*this drug is a combination of a Sulfa and a Salicylate
Enbrel (entanercept)

MOA
Indication
Dose
Drugs used in conjunction
Side effects
Black Box Warning
Drug Interactions
MOA - recombinant DNA-derived protein composed of tumer necrosis factor receptor (TNFR) linked to the Fc portion of human IgG1. Etanercept binds TNF and blocks its interaction with cell surface receptors. TNF plays an important role in the inflammatory processes and the resulting joint pathology of RA, JIA, ankylosing spondlitis, and plaque psoriasis

Indication - RA, JIA, AS, plaque psoriasis

Dose - 50 mg SC inj. once weekly

Drugs used in conjunction - methotrexate and steroids

Side effects - chills, cough, fever, sore throat, cloudy urine, pinkish hematuria

Black Box Warning - test for TB prior to treatment

**FDA has determined that TB is a potential ADR from treatment iwth TNF-alpha antagonists

Drug Interactions:
NO LIVE VACCINES
Anakinra - increased rsk of serious infection
Abatacept - increased rsk of ADR
Cyclophosphamide - DO NOT DO IT
Remicade (infliximab)

MOA
Indication
Dose
Blackbox Warning
MOA - blocks the immune systems overproduction of TNF-alpha (TNF ANTAGONIST)

Indication: RA, psoriatic arthritis, plaque arthritis, ankylosing spondylitis, chrohns disease, ulcerative colitis

Dose -
RA - 3mg/kg IV follo with doses at 2 & 6 wks; then q 9 wks

Chron's - 5mg/kg at 0, 2, 6 wks, then every 8 wks

*if no response by wk 14, D/C

BBW: check for TB; invasive fungal infections, opportunistic infections
Humira (adalimumab)

MOA
Indication
Dose
BBW
MOA - TNF antagonist

Indication - RA, JIA, Psoriatic arthritis, plaque psoriasis, alkylosing spondylitis, chron's

Dose
RA - 40 mg q other wk

May be used with MTX, NSAIDs, other DMARDs, glucocorticoids, salicylates

BBW: check for TB, invasive fungal, opportunistic infections