Professional Documents
Culture Documents
Plavix Clopidogrel Tab OD Blocks ADP Reduction of - Hypersensitivity. - Patients who may be at - Assess for symptoms
receptors which atherosclerotic events in - Severe liver risk of increase of stroke, MI during
prevent fibrinogen patients with impairment. bleeding from trauma, treatment.
binding at the site atherosclerosis documented - Active pathological surgery, or other - Monitor signs of
and thereby reduce by recent stoke, myocardial bleeding e.g. peptic pathological conditions. bleeding;
the possibility of infarction, or established ulcer and - Elective surgery. hemoglobin and
platelet adhesion peripheral arterial disease. intracranial - Patients who have hematocrit
and aggregation. hemorrhage. lesions with a periodically.
- Pregnancy and propensity to bleeding. - Monitor liver
lactation. - Patients with moderate function studies:
hepatic disease who AST, ALT, bilirubin,
may have bleeding creatinine if patient
diatheses. is on long term
therapy; thrombo-
cytopenia may occur.
CONTRAINDICATIONS: Hypersensitivity to insulin; during episodes of hypoglycemia in clients sensitive to any component of the product
NURSING CONSIDERATIONS: Assess for S/S of hypoglycemia (drowsiness, chills, confusion, anxiety, cold sweats, cool pale skin, excessive hunger, nausea,
headache, irritability, shakiness, rapid pulse, unusual tiredness or weakness); assess S/S for hyperglycemia (thirst, polydipsia, polyuria, drowsiness, blurred vision,
loss of appetite, fruity odor to breath, flushed dry skin); weigh client to determine amount to be given; monitor glucose levels carefully in elderly and with hepatic or
renal impairment; assess injection sites, monitor VS (many more considerations; too many to list)
CLASSIFICATION: Antifungal
ACTION: Is highly selective inhibitor of fungal cytochrome P450 and sterol C-14 alpha-demethylation; loss of normal sterols correlates with accumulation of 14
alpha-methyl sterols in fungi and may be responsible for the fungistatic activity; decrease in cell wall integrity and extrusion of intracellularmaterial, leading to
death
INDICATIONS: Oropharyngeal and esophageal candidiasis; serious systemic candidal infection (including UTIs, peritonitis, candidemia, disseminated candidiasis,
and pneumonia); cryptococcal meningitis
USUAL DOSAGE: Candidal UTI and peritonitis – 50-200 mg/day: oropharyngeal or esophageal candidiasis – 150 mg as single oral dose
ADVERSE REACTIONS: Following single doses: headache, nausea, abdominal pain, diarrhea, angioedema; following multiple doses: Nausea, headache, skin
rash, vomiting, abdominal pain, serious hepatic reactions, seizures
INTERACTIONS: Benzodiazepines – ↑ and prolonged serum levels → CNS depression and psychomotor impairment; Glyburide – ↑ plasma glyburide levels
related to ↓ liver breakdown; Glipizide – ↑ plasma glipizide levels related to ↓ liver breakdown; oral contraceptives – possible ↑ or ↓ plasma levels of ethinyl
estradiol and levonorgestrel; protease inhibitors – possible ↑ protease inhibitor levels with possible ↑ toxicity; MANY MORE
NURSING CONSIDERATIONS: Daily dose same for either IV or PO; store tablets under 30ºC (86ºF); loading dose of twice daily dose is recommended for first
day to obtain plasma levels close to steady state by second day; due to long half-life, once daily dosing (either IV or PO) is possible; do not use IV solution if
cloudy, precipitated, or seal broken; do not exceed continuous IV infusion rate of 200 mg/hr; check site frequently for extravasation/necrosis; describe clinical
presentation of fungal infection
ACTION: Has both alpha- and beta-adrenergic blocking activities; decreases cardiac output, reduces exercise- or isoproterenol-induced tachycardia, reduces reflex
orthostatic hypotension, causes vasodilation, and reduces peripheral vascular resistance; BP is lowered more in the standing than in the supine position; significantly
lowers plasma resin activity when given for at least 4 weeks
INDICATIONS: Essential hypertension used either alone or in combination with other antihypertensive drugs, especially thiazide diuretics; mild to severe heart
failure of ischemic or cardiomyopathic origin, used with diuretics, ACE inhibitors, and digitalis to increase survival and reduce risk of hospitalization; reduce CV
mortality in clinically stable clients who have survived an acute MI and have a left ventricular ejection fraction of 40% or less
INTERACTIONS: Antidiabetic agents - ↑ hypoglycemic effects R/T beta blockage; Clonidine – potentiation of BP and heart rate lowering effects; Cyclosporine -
↑ cyclosporine blood levels R/T ↓ liver breakdown; Digoxin - ↑ digoxin levels
CONTRAINDICATIONS: Clients with NYHA class IV decompensated cardiac failure, bronchial asthma, or related bronchospastic conditions, second- or third-
degree AV block, SSS (unless pacemaker is in place), cargiogenic shock, severe bradycardia, drug hypersensitivity; hepatic impairment; lactation
NURSING CONSIDERATIONS: Full antihypertensive effect seen within 7-14 days; addition of diuretic can produce additive effects and exaggerate orthostatic
effect; treat fluid retention with increased dose of diuretics, whether or not heart failure symptoms have worsened; reduce dosage if bradycardia (HR less than 55
bpm) occurs; take as prescrivbed with food, slows absorption/decreases orthostatic effects; avoid OTC agents; avoid activities that require mental acuity until drug
effects realized; do not stop abruptly; R/T beta-blocking activity (esp. with ischemic heart disease)