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Cardio 1 Drugs 3
| Generic | Brand | Indication | Class | MOA | Dose | Boxed Warning |
|---|---|---|---|---|---|---|
| amiodarone | Pacerone, Nexterone | Atrial fibrillation | Antiarrythmic Agent, Class III | primarily inhibits K+ channels, thus increasing action potential duration, leading to a prolonged effective refractory period in cardiac myocytes and reducing myocyte excitability | 100 - 200 mg PO once daily | Life- threatening arrythmias (tablet), Pulmonary toxicity (tablet), Hepatotoxicity (tablet), Worsened arrhythmia (tablet) |
| apixaban | Eliquis | Atrial fibrillation (stroke prevention), Venous Thromboembolism (VTE) prophylaxis and treatment | Anticoagulant, Factor Xa inhibitor | inhibits Factor Xa, thus interrupting the conversion of prothrombin to thrombin, thus preventing thrombin converting fibrinogen to fibrin,and ultimately preventing blood clot formation | A Fib: 5 mg PO BID VTE treatment: 10 mg PO BID for 7 days followed by 5 mg PO BID VTE prophyalxis: 2.5 mg PO BID | Spinal/Epidural hematomas; Premature discontinuation increases the risk of thrombotic events |
| aspirin | N/A | Antiplatelet | Antiplatelet agent, Nonsteroidal Anti-Inflammatory Drugs (NSAID) Salicylate | inhibits COX-1 in platelets, preventing thromboxane A2 formation, thus ultimately preventing platelet aggregation and clot formation | 81 mg PO once daily | None |
| atorvastatin | Lipitor | Hypercholesterolemia | Antilipemic agent, HMG-CoA reductase inhibitor | inhibits the enzyme HMG-CoA reductase, thus inhibiting cholesterol synthesis | 10 - 80 mg PO once daily | None |
| clopidogrel | Plavix | Acute coronary syndrome, Ischemic stroke | Antiplatelet, P2Y12 Inhibitor | inhibits the P2Y12 receptor, preventing ADP binding to it, ultimately inhibiting platelet aggregation | 75 mg PO once daily | Diminished antiplatelet effect in patients with two loss-of-function alleles of the CYP2C19 gene |
| dabigatran | Pradaxa | Atrial fibrillation (stroke prevention), Venous Thromboembolism (VTE) prophylaxis and treatment | Anticoagulant, Direct thrombin inhibitor | inhibits thrombin, thus preventing conversion of fibrinogen to fibrin, and ultimately preventing blood clot formation | A Fib: 150 mg PO BID VTE treatment: 150 mg PO BID | Thrombotic events, Spinal/Epidural hematoma |
| digoxin | Lanoxin | Atrial fibrillation, Heart failure with reduced ejection fraction | Antiarrhythmic agent, Cardiac Glycoside | inhibits myocardial Na+/K+ ATPase, thus raising Na+ levels, leading to Ca2+ influx into myocardial cells. Extra Ca2+ increases force of contraction. | 0.0625 - 0.25 mg PO once daily | None |
| enoxaparin | Lovenox | Venous Thromboembolism (VTE) prophylaxis and treatment | Anticoagulant, Low Molecular Weight Heparin | binds to and potentiates antithrombin III, thus forming a complex that inactivates Factor Xa, ultimately preventing thormbin, fibrin and clot formation. Inhibits thrombin to a lesser degree than heparin | VTE Prophylaxis: 40 mg subcutaneously once daily VTE Treatment: 1 mg/kg subcutaneously Q12H | Spinal/Epidural hematoma |
| ezetimibe | Zetia | Hypercholesterolemia | Antilipemic agent, Cholesterol Absorption Inhibitor | inhibits intestinal NPC1L1, thus preventing intestinal cholesterol absorption, ultimately loweing hepatic cholesterol and leading to the liver clesaring more LDL from the blood | 10 mg PO once daily | None |
| fenofibrate | Tricor | Hypertriglyceridemia | Antilipemic agent, Fibric Acid | activates PPAR-alpha receptors, leading to increases lipolysis and HDL, and a decrease in triglyceride synthesis and LDL | 48 - 145 mg PO once daily | None |
| heparin | N/A | Atrial fibrillation (stroke prevention), Venous Thromboembolism (VTE) prophylaxis and treatment | Anticoagulant | binds to and potentiates antithrombin III, thus forming a complex that inactivates Factor Xa, ultimately preventing thormbin, fibrin and clot formation. Also inhibits thrombin | VTE Prophylaxis: 5000 units subcutaneously Q8-12H VTE Treatment: 80 units/kg bolus followed by a continuous infusion of 18 units/kg/hour | None |
| omega-3-acid ethyl esters | Lovaza | Hypertriglyceridemia | Antilipemic agent, Omega-3 Fatty Acids | lower circualting triglycerides by reducing hepatic VLDL synthesis & accelerating triglyceride clearance | 4 g PO once daily | None |
| pravastatin | Pravachol | Hypercholesterolemia | Antilipemic agent, HMG-CoA reductase inhibitor | inhibits the enzyme HMG-CoA reductase, thus inhibiting cholesterol synthesis | 40 - 80 mg PO once daily | None |
| rivaroxaban | Xarelto | Atrial fibrillation (stroke prevention), Venous Thromboembolism (VTE) prophylaxis and treatment | Anticoagulant, Factor Xa inhibitor | inhibits Factor Xa, thus interrupting the conversion of prothrombin to thrombin, thus preventing thrombin converting fibrinogen to fibrin,and ultimately preventing blood clot formation | A Fib: 20 mg PO once daily VTE treatment: 15 mg PO BID for 21 days followed by 20 mg PO once daily VTE prophylaxis: 10 mg PO once daily | Spinal/Epidural hematomas; Premature discontinuation increases the risk of thrombotic events |
| rosuvastatin | Crestor | Hypercholesterolemia | Antilipemic agent, HMG-CoA reductase inhibitor | inhibits the enzyme HMG-CoA reductase, thus inhibiting cholesterol synthesisinhibits the enzyme HMG-CoA reductase, thus inhibiting cholesterol synthesis | 5 - 40 mg PO once daily | None |
| simvastatin | Zocor | Hypercholesterolemia | Antilipemic agent, HMG-CoA reductase inhibitor | inhibits the enzyme HMG-CoA reductase, thus inhibiting cholesterol synthesis | 10 - 40 mg PO once daily | None |
| ticagrelor | Brilinta | Acute coronary syndrome | Antiplatelet, P2Y12 Inhibitor | inhibits the P2Y12 receptor, preventing ADP binding to it, ultimately inhibiting platelet aggregation | 90 mg PO BID | Bleeding Risk; Diminshed antiplatelet effect when given in combination with aspirin doses > 100 mg daily |
| warfarin | Coumadin | Atrial fibrillation (stroke prevention), Venous Thromboembolism (VTE) treatment | Anticoagulant, Vitamin K Antagonist | inhibits vitamin K epoxide reductase, thus depleting endogenous vitamin K, which is essential in the synthesis of of clotting factors | 1-10 mg PO once daily - Individualized dosing | Bleeding Risk |