Action: inhibits hepatic glucose production and increases
Sensitivity to peripheral tissue to insulin Indication: Management of type 2 diabetes mellitus; may be used with diet, insulin, or sulfonylurea oral hypoglycemics. Adverse Effect: heart failure, lactic acidosis, thrombocytopenia Nursing Implications: monitor for hypoglycemic reactions: hyperglycemic reactions after meals, CBC and other labs (A1c) Lisinopril (Prinivil, Zestril) Indication: Alone or with other agents in the management of hypertension. Adverse effect: CNS: dizziness, fatigue, headache, weakness. Resp: cough. CV: hypotension, chest pain.GI: abdominal pain, diarrhea, nausea, vomiting. GU: erectile dysfunction, impaired renal function. Derm: rashes. F and E hyperkalemia. Misc: ANGIOEDEMA. Nursing Implication: Hypertension: Monitor BP and pulse frequently during initial dosage adjustment and periodically during therapy. Notify health care professional of significant changes. Monitor frequency of prescription refills to determine compliance. Assess patient for signs of angioedema (dyspnea, facial swelling). Heart Failure: Monitor weight and assess patient routinely for resolution of fluid overload (peripheral edema, rales/crackles, dyspnea, weight gain, jugular venous distention). Simvastatin (Zocor) Indication: Adjunctive management of primary hypercholesterolemia and mixed dyslipidemias. Secondary prevention of myocardial infarction, coronary revascularization, stroke, and cardiovascular mortality in patients with clinically evident coronary heart disease. Adverse effect: CNS: dizziness, headache, insomnia, weakness. GI: abdominal cramps, constipation,diarrhea, flatus, heartburn, altered taste, drug-induced hepatitis, dyspepsia, liver enzymes, nausea, pancreatitis. GU: erectile dysfunction. Derm: rashes, pruritus.MS: RHABDOMYOLYSIS, arthralgia, myalgia, myopathy ( risk with 80 mg dose).Misc: hypersensitivity reactions. Nursing Implication: Obtain a diet history, especially with regard to fat consumption. Evaluate serum cholesterol and triglyceride levels before initiating, after 46 wk. of therapy, and periodically thereafter. Avoid grapefruit and grapefruit juice during therapy; may increase risk of toxicity.