CV pharm Flashcards
amlodipine moa
block voltage-dependent L-type calcium channels of cardiac and smooth muscle, thereby reduce muscle contractility
dihydropyridine CCBs (drugs)
amlodipine, nifedipine, nimodipine
non-dihydropyridine CCBs (drugs)
diltiazem and verapamil
CCBs for vascular smooth muscle
amlodipine=nifedipine>diltiazem>verapamil
CCBs for the heart
verapamil>diltiazem>amlodipine=nifedipine
hydralazine MOA
increases cGMP, causing smooth muscle relaxation, vasodilates arterioles > veins; reduces afterload
clinical use for dihydropyridines
hypertension, angina (including Prinzmetal), Raynaud phenomenon
clinical use for non-dihydropyridine CCBs
hypertension, angina, atrial fibrillation/flutter
clinical use for nimodipine
subarachnoid hemorrhage; prevents cerebral vasospasm
clinical use for hydralazine
severe hypertension, CHF, first line therapy for HTN in pregnancy, with methyldopa; frequently coadministered with a beta-blocker to prevent reflex tachycardia
hydralazine adverse effects
compensatory tachycardia (contraindicated in angina/CAD), fluid retention, nausea, headache, angina, lupus-like syndrome
statin adverse effect
hepatotoxicity, rhabdomyolysis, esp when used with fibrates
can cause cyanide toxicity
nitroprusside
fenoldopam
D1 agonist; causes vasodilation; decreases BP and increases natriruesis
statin moa
inhibits HGM-CoA reductase, blocking conversion of HMG-CoA to mevalonate, a cholesterol precursor
Niacin moa
inhibits lipolysis in adipose tissue; reduces hepatic VLDL synthesis
niacin adverse effects
flushing, decreased by aspirin or long term use
hyperglycemia + acanthosis nigricans
hyperuricemia - exacerbates gout
bile acid resins adverse effects
decrease absorption of fat soluble vitamins, increase incidence of cholesterol gallstones
ezetimibe moa
prevents cholesterol absorption in the brush border
ezetimibe adverse effects
diarrhea; increase in LFTs
fibrates moa
upregulate LPL, increasing TG clearance; activates PPAR-alpha to induce HDL synthesis
fibrates adverse effects
myositis; increased risk with concurrent statin use, hepatotoxicity, increase in LFTs, cholesterol gallstones (esp. when used with bile resins)