Cardiovascular
47 source-linked study cards in this body system.
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Drug classes in this body system
ACE inhibitors
Lisinopril · Lisinopril / Hydrochlorothiazide · Amlodipine / Benazepril · Benazepril · Enalapril · Ramipril
Angiotensin II receptor blockers
Losartan · Losartan / Hydrochlorothiazide · Valsartan · Olmesartan / Amlodipine / Hydrochlorothiazide · Irbesartan · Telmisartan · Sacubitril / Valsartan
Beta-adrenergic blockers
Metoprolol · Carvedilol · Atenolol · Propranolol · Nebivolol · Bisoprolol · Labetalol
Dihydropyridine calcium channel blockers
Amlodipine · Olmesartan / Amlodipine / Hydrochlorothiazide · Amlodipine / Benazepril
Non-dihydropyridine calcium channel blockers
Verapamil
HMG-CoA reductase inhibitors
Atorvastatin · Rosuvastatin · Simvastatin · Pravastatin · Lovastatin
Loop diuretics
Furosemide · Torsemide · Bumetanide
Thiazide and thiazide-like diuretics
Hydrochlorothiazide · Lisinopril / Hydrochlorothiazide · Losartan / Hydrochlorothiazide · Olmesartan / Amlodipine / Hydrochlorothiazide · Triamterene / Hydrochlorothiazide · Chlorthalidone
Alpha-1 adrenergic blockers
Carvedilol · Labetalol
P2Y12 platelet inhibitors
Ticagrelor
How each medicine works
Medicines in this body system: 47 · in a drug class: 34 · drug classes: 10
| Atorvastatin — Selectively and competitively inhibits HMG-CoA reductase, a key enzyme in cholesterol synthesis. In animal models, increased hepatic LDL receptors also contribute to LDL uptake and breakdown. |
| Lisinopril — Inhibits angiotensin-converting enzyme, blocking conversion of angiotensin I to angiotensin II and suppressing the renin-angiotensin-aldosterone system. |
| Amlodipine — Dihydropyridine calcium antagonist that inhibits transmembrane influx of calcium ions into vascular smooth muscle and cardiac muscle. |
| Metoprolol — Beta-1 selective (cardioselective) adrenergic receptor blocker without intrinsic sympathomimetic activity; blocks beta-2 at higher levels. |
| Losartan — Losartan and its active metabolite block the vasoconstrictor and aldosterone-secreting effects of angiotensin II at its receptor. |
| Rosuvastatin — Inhibits HMG-CoA reductase, the rate-limiting enzyme converting HMG-CoA to mevalonate, a precursor of cholesterol. |
| Hydrochlorothiazide — Affects distal renal tubular electrolyte reabsorption and increases sodium and chloride excretion. The selected label describes the mechanism of its antihypertensive effect as unknown. |
| Simvastatin — Prodrug hydrolyzed to simvastatin acid, which inhibits HMG-CoA reductase, the rate-limiting enzyme of cholesterol synthesis. |
| Furosemide — Inhibits sodium and chloride reabsorption in the loop of Henle and the proximal and distal tubules. |
| Carvedilol — Racemic mixture: nonselective beta-blockade from the S(-) enantiomer and alpha-1 blockade from both enantiomers; no intrinsic sympathomimetic activity. |
| Spironolactone — Competitively blocks aldosterone receptors in the distal tubule: more sodium and water excreted, potassium retained. |
| Pravastatin — Reversibly inhibits HMG-CoA reductase, the rate-limiting enzyme converting HMG-CoA to mevalonate, a cholesterol precursor. |
| Ezetimibe — Blocks the NPC1L1 sterol transporter at the intestinal brush border, reducing cholesterol absorption and hepatic delivery. |
| Atenolol — Beta-1 selective adrenergic blocker without membrane stabilizing or intrinsic sympathomimetic activity; selectivity lost at higher doses. |
| Propranolol — Nonselective beta blockade generally reduces myocardial oxygen demand in angina. Its antihypertensive mechanism is not established; reduced cardiac output, renin release and sympathetic outflow may contribute. |
| Lisinopril / Hydrochlorothiazide — Lisinopril inhibits ACE, lowering angiotensin II and aldosterone; hydrochlorothiazide is a thiazide diuretic. |
| Losartan / Hydrochlorothiazide — Losartan selectively blocks angiotensin II binding at AT1 receptors; hydrochlorothiazide increases renal sodium and chloride excretion. |
| Valsartan — Selectively blocks angiotensin II binding to AT1 receptors, inhibiting its vasoconstrictor and aldosterone-secreting effects. |
| Olmesartan / Amlodipine / Hydrochlorothiazide — Olmesartan blocks angiotensin II effects, amlodipine blocks calcium entry into vascular smooth muscle, and HCTZ promotes sodium and chloride excretion. |
| Fenofibrate — Fenofibric acid activates PPAR-alpha, increasing lipoprotein lipase activity and lowering apo C-III, which reduces triglyceride-rich particles. |
| Diltiazem — Therapeutic effects are believed to relate to inhibition of calcium influx in cardiac and vascular smooth muscle; vascular relaxation lowers peripheral resistance and blood pressure. |
| Hydralazine — The precise mechanism is incompletely understood; hydralazine apparently lowers blood pressure through direct vascular smooth-muscle relaxation and altered cellular calcium handling, preferentially dilating arterioles. |
| Clonidine — Stimulates alpha-adrenoreceptors in the brain stem, reducing sympathetic outflow, peripheral resistance, heart rate and blood pressure. |
| Triamterene / Hydrochlorothiazide — HCTZ blocks renal tubular sodium and chloride reabsorption; triamterene inhibits distal sodium reabsorption, reducing potassium loss. |
| Chlorthalidone — A long-acting oral diuretic that increases sodium and chloride excretion. Its site of action appears to be the cortical diluting segment of the ascending limb of Henle’s loop; the antihypertensive mechanism is not wholly clear. |
| Isosorbide Mononitrate — Relaxes vascular smooth muscle, dilating peripheral arteries and especially veins. |
| Nifedipine — Inhibits calcium influx, dilating coronary arteries and arterioles and inhibiting coronary artery spasm. |
| Lovastatin — Lactone prodrug hydrolyzed to its beta-hydroxyacid, which inhibits HMG-CoA reductase, an early step in cholesterol synthesis. |
| Nitroglycerin (sublingual) — Releases nitric oxide, activating guanylate cyclase; rising cGMP dephosphorylates myosin light chains, relaxing vascular smooth muscle. |
| Irbesartan — Blocks the vasoconstrictor and aldosterone-secreting effects of angiotensin II at its receptor. |
| Nebivolol — Antihypertensive mechanism not definitively established; may involve lower heart rate and contractility, less renin, vasodilation. |
| Amlodipine / Benazepril — Benazepril inhibits ACE, lowering angiotensin II and aldosterone; amlodipine is a dihydropyridine calcium channel blocker. |
| Benazepril — Benazeprilat inhibits ACE, blocking conversion of angiotensin I to angiotensin II and lowering aldosterone. |
| Torsemide — Animal micropuncture studies show inhibition of the Na+/K+/2Cl− carrier from the lumen of the thick ascending loop of Henle, producing diuresis. |
| Amiodarone — Class III antiarrhythmic with properties of all four Vaughan Williams classes; blocks Na+ channels, antisympathetic. |
| Telmisartan — Blocks angiotensin II at the AT1 receptor, reducing vasoconstriction and aldosterone release. |
| Sacubitril / Valsartan — Sacubitril (via LBQ657) inhibits neprilysin; valsartan blocks the AT1 receptor. |
| Verapamil — Lowers blood pressure by decreasing systemic vascular resistance, usually without reflex tachycardia. |
| Enalapril — Hydrolyzed to enalaprilat, which inhibits ACE, blocking angiotensin II formation and aldosterone secretion. |
| Ramipril — Ramiprilat inhibits ACE, blocking conversion of angiotensin I to angiotensin II and reducing aldosterone. |
| Bisoprolol — Beta-1-selective adrenoceptor blocker without significant membrane-stabilizing or intrinsic sympathomimetic activity at therapeutic doses. |
| Ticagrelor — Reversibly binds the platelet P2Y12 ADP receptor, preventing signal transduction and platelet activation. |
| Labetalol — Combines selective competitive alpha1 blockade with nonselective competitive beta blockade. |
| Flecainide — Class IC membrane-stabilizing agent with local anesthetic activity; slows intracardiac conduction, most in the His-Purkinje system. |
| Evolocumab — Human IgG2 antibody against PCSK9; blocks PCSK9 binding to LDL receptors, leaving more receptors to clear LDL-C. |
| Icosapent Ethyl — EPA ethyl ester; thought to reduce hepatic VLDL-TG synthesis and/or secretion and to enhance TG clearance from VLDL. |
| Bumetanide — Loop diuretic; inhibits sodium and chloride reabsorption in the ascending limb of the loop of Henle. |
Each summary is the mechanism line from the medicine’s study card.
Listed most often on cards in this body system
Used for
Hypertension · 7/47: Amlodipine, Atenolol, Diltiazem, Clonidine, Irbesartan, Nebivolol, Torsemide
Hypertension in adults · 6/47: Metoprolol, Chlorthalidone, Telmisartan, Ramipril, Bisoprolol, Labetalol
Hypertension in adults and children aged 6 years and older · 3/47: Lisinopril, Losartan, Valsartan
Common side effects
Dizziness · 26/47: Lisinopril, Amlodipine, Metoprolol, Losartan, Furosemide, Carvedilol, Spironolactone, Atenolol, Lisinopril / Hydrochlorothiazide, Losartan / Hydrochlorothiazide (+16)
Headache · 22/47: Lisinopril, Rosuvastatin, Simvastatin, Spironolactone, Pravastatin, Lisinopril / Hydrochlorothiazide, Valsartan, Olmesartan / Amlodipine / Hydrochlorothiazide, Hydralazine, Triamterene / Hydrochlorothiazide (+12)
Nausea · 10/47: Rosuvastatin, Hydrochlorothiazide, Simvastatin, Furosemide, Hydralazine, Triamterene / Hydrochlorothiazide, Chlorthalidone, Verapamil, Labetalol, Bumetanide
Fatigue · 10/47: Carvedilol, Ezetimibe, Lisinopril / Hydrochlorothiazide, Valsartan, Olmesartan / Amlodipine / Hydrochlorothiazide, Triamterene / Hydrochlorothiazide, Nebivolol, Enalapril, Ramipril, Labetalol
Cough · 9/47: Lisinopril, Lisinopril / Hydrochlorothiazide, Losartan / Hydrochlorothiazide, Amlodipine / Benazepril, Benazepril, Sacubitril / Valsartan, Enalapril, Ramipril, Bisoprolol
Hypotension · 7/47: Lisinopril, Carvedilol, Valsartan, Torsemide, Sacubitril / Valsartan, Verapamil, Bumetanide
Constipation · 7/47: Rosuvastatin, Simvastatin, Diltiazem, Clonidine, Lovastatin, Verapamil, Icosapent Ethyl
Diarrhea · 5/47: Atorvastatin, Pravastatin, Ezetimibe, Telmisartan, Bisoprolol
Warnings
Myopathy / rhabdomyolysis · 5/47: Atorvastatin, Rosuvastatin, Simvastatin, Pravastatin, Ezetimibe
Immune-mediated necrotizing myopathy · 4/47: Atorvastatin, Rosuvastatin, Simvastatin, Pravastatin
Angioedema · 4/47: Lisinopril, Benazepril, Sacubitril / Valsartan, Ramipril
Hyperkalemia · 4/47: Lisinopril, Losartan, Spironolactone, Benazepril
Acute liver failure or decompensated cirrhosis · 3/47: Atorvastatin, Rosuvastatin, Simvastatin
Renal impairment · 3/47: Lisinopril, Benazepril, Ramipril
Hypotension in volume-depleted patients · 3/47: Losartan, Losartan / Hydrochlorothiazide, Olmesartan / Amlodipine / Hydrochlorothiazide
Hypotension · 3/47: Valsartan, Telmisartan, Sacubitril / Valsartan
Interactions
Lithium · 14/47: Lisinopril, Losartan, Furosemide, Spironolactone, Losartan / Hydrochlorothiazide, Valsartan, Olmesartan / Amlodipine / Hydrochlorothiazide, Triamterene / Hydrochlorothiazide, Chlorthalidone, Irbesartan (+4)
NSAIDs · 10/47: Lisinopril, Losartan, Spironolactone, Losartan / Hydrochlorothiazide, Valsartan, Olmesartan / Amlodipine / Hydrochlorothiazide, Amlodipine / Benazepril, Benazepril, Torsemide, Ramipril
Digoxin · 3/47: Atorvastatin, Amiodarone, Telmisartan
Boxed warning
19/47: Lisinopril, Losartan, Atenolol, Lisinopril / Hydrochlorothiazide, Losartan / Hydrochlorothiazide, Valsartan, Olmesartan / Amlodipine / Hydrochlorothiazide, Triamterene / Hydrochlorothiazide, Irbesartan, Amlodipine / Benazepril (+9)
Same boxed-warning wording on: Lisinopril, Losartan
Same boxed-warning wording on: Lisinopril / Hydrochlorothiazide, Losartan / Hydrochlorothiazide, Valsartan
Same boxed-warning wording on: Olmesartan / Amlodipine / Hydrochlorothiazide, Irbesartan
Same boxed-warning wording on: Benazepril, Telmisartan, Sacubitril / Valsartan, Enalapril, Ramipril
An item counts as shared only when both cards use the same wording. If a card does not list an item, that is not a statement that the effect never occurs.