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Methotrexate - Classification
Disease-modifying antirheumatic drug (DMARD)
Methotrexate - Therapeutic use
Decreases joint inflammation and, subsequently, joint damage
Methotrexate - Adverse drug reaction
Hepatic fibrosis, increased risk of infection, liver damage, gastrointestinal ulceration, pulmonary fibrosis, bone marrow suppression
Methotrexate - Nursing intervention
Monitor for decreased platelets, red and white blood cell counts, signs and symptoms of infection, liver function, gastrointestinal bleeding, respiratory distress
Methotrexate - Administration
Give once a week via route prescribed (oral, subcutaneous, or intramuscular); folic acid supplement may be prescribed to decrease risk of toxicity
Methotrexate - Contraindication
Pregnancy, liver insufficiency or hepatitis, renal insufficiency
Methotrexate - Client education
Takes 3-6 weeks to feel effects, can take several months to feel full effect; drink 2-3 L of fluids per day
Raloxifene - Classification
Selective estrogen receptor modulator (SERM)
Raloxifene - Therapeutic use
Postmenopausal osteoporosis
Raloxifene - Adverse drug reaction
Increased risk of deep vein thrombosis (DVT) and pulmonary emboli, hot flashes, stroke
Raloxifene - Nursing intervention
Observe for signs and symptoms of thromboembolism, monitor bone density
Raloxifene - Administration
Give orally daily; may be given with or without food
Raloxifene - Contraindication
Teratogenic, lactation, current and past history of deep vein thrombosis
Raloxifene - Client education
Report pain in the calf or difficulty breathing; warn clients that hot flashes may occur
Colchicine - Classification
Anti-inflammatory agent
Colchicine - Therapeutic use
Abort an acute gout attack in response to precursor findings
Colchicine - Adverse drug reaction
Mild gastrointestinal distress which can progress to gastrointestinal toxicity, bone marrow suppression
Colchicine - Nursing intervention
Monitor uric acid levels, CBC, UA, BUN
Colchicine - Administration
Give orally for gout treatment
Colchicine - Contraindication
Severe renal, cardiac, hepatic, or gastrointestinal dysfunction
Colchicine - Client education
Avoid eating or drinking grapefruit or foods high in purine; if severe gastrointestinal distress occurs, stop this medication; take with food
Alendronate - Classification
Bisphosphonate
Alendronate - Therapeutic use
Prevention and treatment of postmenopausal osteoporosis, age-related osteoporosis in men, Paget's disease
Alendronate - Adverse drug reaction
Esophagitis, gastrointestinal disturbances, muscle and joint pain, eye pain, and vision changes
Alendronate - Nursing intervention
For 30 minutes after taking the drug, have clients remain in upright position and avoid eating or drinking anything other than water
Alendronate - Administration
Give drug 30 minutes before breakfast with a full glass of water; have client sit or stand for 30 minutes after administration
Alendronate - Contraindication
Esophageal strictures/disorders or difficulty swallowing, clients unable to sit up for 30 minutes after administration, renal insufficiency, hypocalcemia
Alendronate - Client education
Take with a full glass of water, sit or stand up, avoid eating or drinking anything other than water, and avoid taking calcium supplements or antacids for 30 minutes after taking the drug.
Prednisone - Classification
Glucocorticoid
Prednisone - Therapeutic use
Symptomatic relief of pain and inflammation for a wide variety of disorders; delay progression of some disorders, such as rheumatoid arthritis
Prednisone - Adverse drug reaction
Suppression of adrenal function, risk of infection, osteoporosis, fluid retention, gastrointestinal discomfort
Prednisone - Nursing intervention
Monitor blood glucose levels (especially for clients who have diabetes mellitus), gastrointestinal bleeding, signs of infection, edema, crackles in the lungs, generalized weakness
Prednisone - Administration
Give PO or as a joint injection
Prednisone - Contraindication
Recent live virus immunization, systemic fungal infection, cataracts
Prednisone - Client education
Avoid taking NSAIDs, take with food or meals, short-term therapy can be used while waiting for peak therapeutic effect of DMARDs
Allopurinol - Classification
Agent for hyperuricemia
Allopurinol - Therapeutic use
Hyperuricemia due to chronic tophaceous gout
Allopurinol - Adverse drug reaction
Hypersensitivity syndrome, gastrointestinal disturbances, kidney or liver damage, hepatitis, may increase gout attacks, metallic taste in the mouth
Allopurinol - Nursing intervention
Monitor for symptoms of hypersensitivity syndrome, CBC, unusual taste sensations; stop drug therapy immediately for signs of hypersensitivity syndrome
Allopurinol - Administration
Give orally or IV; monitor uric acid levels (initially every 1 to 2 weeks to establish the appropriate dosage)
Allopurinol - Contraindication
Hypersensitivity to the medication, idiopathic hemochromatosis
Allopurinol - Client education
Report fever, rash, abdominal pain, swelling, or low urine output immediately and stop taking the drug; take with food
Calcium Citrate - Classification
Calcium supplement
Calcium Citrate - Therapeutic use
Hypocalcemia
Calcium Citrate - Adverse drug reaction
Hypercalcemia, nausea, vomiting, constipation, kidney stones
Calcium Citrate - Nursing intervention
Monitor serum calcium, signs of decreased gastric and intestinal motility, urine output in excess of intake, signs of decreased gastric and intestinal motility, flank pain, and blood in urine
Calcium Citrate - Administration
Give orally or IV; give clients glass of water after swallowing
Calcium Citrate - Contraindication
Hypercalcemia, kidney stones, low phosphate levels, cardiac dysrhythmias
Calcium Citrate - Client education
Instruct clients to take 1-2 hours before or after taking other medications such as glucocorticoids, thyroid supplements, and tetracycline and quinolone antibiotics