BP reduction is greatest after peak levels of amlodipine are achieved 6-9 h following oral doses. Atorvastatin is an inhibitor of reductase 3hydroxy-3-methylglutaryl coenzyme a (rmgcoa) is a calcium channel blocking agent that selectively blocks calcium ion reflux across cell membranes of cardiac and vascular smooth muscle without changing serum calcium concentrations.
BP reduction is greatest after peak levels of amlodipine are achieved 6-9 h following oral doses. Atorvastatin is an inhibitor of reductase 3hydroxy-3-methylglutaryl coenzyme a (rmgcoa) is a calcium channel blocking agent that selectively blocks calcium ion reflux across cell membranes of cardiac and vascular smooth muscle without changing serum calcium concentrations.
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BP reduction is greatest after peak levels of amlodipine are achieved 6-9 h following oral doses. Atorvastatin is an inhibitor of reductase 3hydroxy-3-methylglutaryl coenzyme a (rmgcoa) is a calcium channel blocking agent that selectively blocks calcium ion reflux across cell membranes of cardiac and vascular smooth muscle without changing serum calcium concentrations.
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DRUG NAME ROUTE OF INDICATION SIDE EFFECTS CONTRAINDICAT SPECIAL CONSIDERATION MECHANISM OF
AND ADMINISTRA ION ACTION
CLASSIFICATI TION AND ON FREQUENCY Amlodipine PO 10 mg once • Treatment of mild to CNS: Light-headedness, Hypersensitivity to • Monitor BP for therapeutic Is a calcium channel (Norvasc) daily moderate hypertension fatigue, headache. amlodipine effectiveness. BP reduction is blocking agent that and angina. GI: Abdominal pain, greatest after peak levels of selectively blocks nausea, flatulence. amlodipine are achieved 6–9 h calcium ion reflux following oral doses. across cell • Monitor for S&S of dose- membranes of cardiac related peripheral or facial and vascular smooth edema that may not be muscle without accompanied by weight gain; changing serum rarely, severe edema may calcium cause discontinuation of drug. concentrations. It • Monitor BP with postural predominantly acts on changes. Report postural the peripheral hypotension. Monitor more circulation, frequently when additional decreasing peripheral antihypertensives or diuretics vascular resistance, are added. and increases cardiac • Monitor heart rate; dose- output. related palpitations (more common in women) may occur. DRUG NAME AND ROUTE OF INDICATION SIDE EFFECTS CONTRAINDICATION SPECIAL MECHANISM OF CLASSIFICATION ADMINISTRATION CONSIDERATION ACTION AND FREQUENCY Atorvastatin PO 20 mg q.d. • Adjunct to diet GI: Abdominal pain, Hypersensitivity to • Monitor for therapeutic Atorvastatin is an (Lipitor) for the reduction constipation, flatulence. atorvastatin, myopathy, effectiveness which is inhibitor of of LDL active liver disease, indicated by reduction in reductase 3- Classifications: cholesterol and unexplained persistent the level of LDL-C. hydroxy-3-methyl- CARDIOVASCULAR triglycerides in transaminase elevations • Lab tests: Monitor lipid glutaryl coenzyme AGENT; LIPID- patients with levels within 2–4 wk A (HMG-CoA), LOWERING AGENT; primary after initiation of therapy which is essential to HMG-COA or upon change in hepatic production hypercholesterole REDUCTASE INHIBITOR (STATIN) mia and mixed dosage; monitor liver of cholesterol. dyslipidemia. functions at 6 and 12 wk Lipitor increases the after initiation or number of hepatic elevation of dose, and low-density-lipid periodically thereafter. (LDL) receptors, • Assess for muscle pain, thus increasing tenderness, or weakness; LDL uptake and and, if present, monitor catabolism of LDL. CPK level (discontinue drug with marked elevations of CPK or if myopathy is suspected). DRUG NAME ROUTE OF INDICATION SIDE EFFECTS CONTRAINDICAT SPECIAL CONSIDERATION MECHANISM OF AND ADMINISTRA ION ACTION CLASSIFICATI TION AND ON FREQUENCY Metoprolol PO 50–100 Management of mild to CNS: Dizziness, fatigue Cardiogenic shock, • Take apical pulse and BP Beta-adrenergic tartrate mg/d in 1–2 severe hypertension GI: Nausea, constipation, sinus bradycardia, before administering drug. blocking agent with (Betaloc) divided doses (monotherapy or in flatulence heart block greater Report to physician significant preferential effect on combination with a than first degree, changes in rate, rhythm, or beta1 adrenoreceptors Classifications: thiazide or vasodilator or overt cardiac failure, quality of pulse or variations located primarily on AUTONOMIC both) right ventricular in BP prior to administration. cardiac muscle. At NERVOUS SYSTEM failure secondary to higher doses, AGENT • Monitor BP, HR, and ECG (SYMPATHOMIMET pulmonary carefully during IV metoprolol also IC); BETA- hypertension. administration. inhibits beta2 ADRENERGIC • Expect maximal effect on BP receptors located ANTAGONIST after 1 wk of therapy. chiefly on bronchial (SYMPATHOLYTIC) • Take several BP readings and vascular ; musculature. ANTIHYPERTENSIV close to the end of a 12 h dosing interval to evaluate Antihypertensive E AGENT adequacy of dosage for action may be due to patients with hypertension, competitive particularly in patients on antagonism of twice daily doses. Some catecholamines at patients require doses 3 times cardiac adrenergic a day to maintain satisfactory neuron sites, drug- control. induced reduction of • Observe hypertensive patients sympathetic outflow with CHF closely for to the periphery, and impending heart failure: to suppression of Dyspnea on exertion, renin activity. orthopnea, night cough, edema, distended neck veins. • Lab tests: Obtain baseline and periodic evaluations of blood cell counts, blood glucose, liver and kidney function. • Monitor I&O, daily weight; auscultate daily for pulmonary rales. • Withdraw drug if patient presents symptoms of mental depression because it can progress to catatonia. Possible symptoms of depression: