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Drugs & Lipoproteins, Heart, Blood, Vascular System 1 & 2
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atorvastatin [class]
Statin
simvastatin [class]
Statin
rosuvastatin [class]
Statin
bezafibrate [class]
Fibrate
cholestyramine [class]
Bile Acid Binding Resin
metoprolol [class]
Beta Antagonist (Beta Blocker)
carvedilol [class]
Non-Selective Beta Antagonist & Alpha-1 Antagonist
amiodarone [class]
Potassium Channel Blocker (Class III Antidysrhythmic)
verapamil [class]
Calcium channel blocker (cardioselective)
diltiazem [class]
Calcium channel blocker (intermediate selectivity)
isoprenaline [class]
Beta Agonist; Positive Inotrope
dobutamine [class]
Beta Agonist; Positive Inotrope
milrinone [class]
Phosphodiesterase Inhibitor
digoxin [class]
Na+/K+ ATPase Inhibitor; Positive Inotrope
heparin / LMW heparin [class]
Anticoagulant
warfarin [class]
Anticoagulant
dabigatrin [class]
Direct Oral Anticoagulant (DOAC); Unilvant Direct thrombin inhibitor
rivaroxaban [class]
Direct Oral Anticoagulant (DOAC)
tissue plasminogen activator (tPa) [class]
Fibrinolytic agent
streptokinase [class]
Fibrinolytic agent
aspirin [class]
Platelet Modifier
clopidogrel [class]
Platelet Modifier
nifedipine [class]
Calcium Channel Blocker
isosorbide mononitrate [class]
Nitrate (oral)
glyceryl trinitrate/nitroglycerin [class]
Nitrate (sublingual)
sodium nitroprusside (SNP) [class]
Nitrate (IV)
captopril [class]
ACE Inhibitor
losartan [class]
Angiotensin Receptor Antagonist/Blocker
prazosin [class]
Alpha-1 antagonist
atorvastatin [MoA]
Inhibits HMG CoA Reductase, decraeses synthesis of cholesterol which promotes uptake of LDL from bloodstream
simvastatin [MoA]
Inhibits HMG CoA Reductase, decraeses synthesis of cholesterol which promotes uptake of LDL from bloodstream
rosuvastatin [MoA]
Inhibits HMG CoA Reductase, decraeses synthesis of cholesterol which promotes uptake of LDL from bloodstream
bezafibrate [MoA]
Agonist at PPAR-alpha receptor, increases LPL activity, increases chylomicron/VLDL catabolism
cholestyramine [MoA]
Absorbs bile acids in intestine and traps there for excretion in faeces, body uses cholesterol to make more bile acids
metoprolol [MoA]
Antagonist at beta-1 adrenoceptors, decreasing cAMP production and calcium entry to cardiac cells
carvedilol [MoA]
Antagonist at beta adrenoceptors (see metoprolol); decreases vasoconstriction via alpha-1 antagonism
amiodarone [MoA]
Slows potassium influx (Phase 3) of cardiac action potential, delays repolarisation phase, slows HR
verapamil [MoA]
Block L-type calcium channels, inhibits cardiac contraction
diltiazem [MoA]
Block L-type calcium channels, inhibits cardiac contraction and vasoconstriction
isoprenaline [MoA]
Agonist at beta-1 and beta-2 receptors, increases cAMP and therefore contractile force
dobutamine [MoA]
Agonist at beta-1 and beta-2 receptors, increases cAMP and therefore contractile force; causes vasoconstriction via alpha-1 to raise blood pressure
milrinone [MoA]
Inhibits PDE 3 to reduce breakdown of cAMP, promotes cardiac contractility and vasodilation
digoxin [MoA]
Inhibits Na+/K+ ATPase, increases intracellular Na which decreases driving force of NCX, results in reduced calcium extrusion
heparin / LMW heparin [MoA]
Activates AT-III-induced inhibition of Factors II and X (LMW heparin mostly via Factor X)
warfarin [MoA]
Inhibits Vitamin K Reductase, preventing redox cycling of warfarin and therefore production of clotting factors
dabigatrin [MoA]
Inhibits activated-thrombin ability to bind to fibrinogen and form fibrin
rivaroxaban [MoA]
Directly inhibits Factor Xa, preventing conversion of prothrombin to thrombin
tissue plasminogen activator (tPa) [MoA]
Binds to fibrin on the clot, activates fibrin-bound plasminogen, plasmin is cleaved, fibrin broken down, clot dissolves
streptokinase [MoA]
Binds to fibrin (on the clot or circulating), activates plasminogen, plasmin is cleaved, fibrin broken down, clot dissolves
aspirin [MoA]
COX1 inhibitor
clopidogrel [MoA]
Inhibits binding of ADP to its platelet receptor
nifedipine [MoA]
Blocks L-type calcium channels, inhibiting vascular smooth muscle contraction
isosorbide mononitrate [MoA]
Breaks down to release NO
glyceryl trinitrate/nitroglycerin [MoA]
Breaks down to release NO
sodium nitroprusside (SNP) [MoA]
Breaks down to release NO
captopril [MoA]
Inhibits ACE, preventing conversion of Ang I to Ang II
losartan [MoA]
Antagonises AT1 receptors to inhibit the actions of Ang II
prazosin [MoA]
Antagonises alpha-1 receptors to block SNS-mediated vasoconstriction