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USMLE
Comprehensive Pharm 3
Question | Answer |
---|---|
what are the symptoms of organophosphate poisoning | DUMBBELSS Diarrhea Urination Miosis Bradycardia Bronchospasm Excitation of skel muscle Lacrimation Sweating Salivation |
antidote to organophosphate poisoning | atropine + pralidoxime |
what is pralidoxime | antagonist used to regenerate active cholinesterase |
MOA of epi in tx of glaucoma | increases outflow of aqueous humor |
MOA brimonidine in tx of glaucoma | (alpha agonist) decreases aqueous humor synth |
MOA beta blockers in tx of glaucoma | decreases aqueous humor secretion |
MOA acetazolamide in tx of glaucoma | decreas aqueous humor secretion d/t decreaed HCO3 |
MAO cholinomimetics in tx of glaucoma | increased outflow of aqueous humor |
which drug should be used in a glaucoma emergency | pilocarpine (direct ACh mimetic) |
MOA latanoprost in tx of glaucoma | PGF-alpha, increases outflow of aqueous humor |
which glaucoma drugs decrease the synth of aqueous humor? | beta-blockers brimonidine acetazolamide |
which glaucoma drugs increase outflow of aqueous humor? | epi cholinomimetics PGF2alpa (latanoprost) |
MOA atropine | muscarinic antagonist |
toxicity of atropine | dry as a bone hot as a hare mad as a hatter red as a beet blind as a bat |
Effects Nitrates have on: EDV BP Contractility HR Ejection time MV O2 | down down up (reflex) up (reflex) down down |
Effects B-blockers have on: EDV BP Contractility HR Ejection time MV O2 | up down down down up down |
effects b-blockers + nitrates have on: EDV BP Contractility HR Ejection time MV O2 | no effect, or down down little, no effect down little/no effect down a lot! |
MOA CCBs | block voltage dependent ca channels of cardiac and smooth muscle, reducing muscle contractility |
In decreasing effect, which CCBs have most effect on vascular smooth muscle? | nifedipine > diltiazem > verapemil |
in decreasign effeect, which CCBs have most effect on heart? | verapamil > diltiazem > nifedipine |
which CCB can't be used for arrhythmias? | nifedipine |
toxicity of CCBs | cardiac depression flushing peripheral edema dizziness constipation |
which CCB is most similar to nitrates in effect? | nifedipine (makes sense... nifedipine works most strongly on vascular smooth muscle) |
which CCB is most similar to b-blockers in effect? | verapamil (makes sense... verapamil works most strongly on heart) |
MOA statins? | HMG-CoA reductase inhibitors blocks formation of cholesterol from HMG-CoA |
MOA niacin | blocks the export of cholesterol from the hepatocyte to the blood |
MOA bile resins | binds cholesterol in the gut so they can't get to the hepatocytes |
MOA ezetimibe | cholesterol absorption blocker so, prevents cholesterol from entering hepatocytes from gut |
MOA fibrates | increases action of lipoprotein lipase, encouraging the breakdown of VLDL --> LDL also decreases hepatic synthesis and secretion of VLDL increases HDL by decreasing TG (results from decreased VLDL) --> decresaed exchange of cholestreryl esters from HDL |
which cholesterol agents affect endogenous production of cholesterol? | fibrates niacin lovastatin |
which cholesterol agents affect absorption of exogenous cholesterol | ezetimibe bise acid resins |
effects of statins on: LDL HDL TGs | down A LOT up down |
effects of niacin on LDL HDL TGs | down a lot (not as much as statins) up A LOT down |
effects of bile acid resins on LDL HDL TGs | down a lot (not as much as statins) none slightly UP |
effects of ezetimibe on LDL HDL TGs | down a lot (not as much as statins) none none |
effects of fibrates on: LDL HDL TGs | down a little up DOWN A FRIGGIN TON! |
what 2 cholesterol drugs, if taken concurrently, will cause rhabdomyolysis | statins and fibrates |
which cholesterol drugs increase LFTs? | your lft's are not SEF (safe) statins ezetimibe fibrates |
which cholesterol drug --> GI discomfort | bile acid resins |
antidote to dig toxicity | anti-dig Fab fragment s slowly normalize K lidocaine cardiac pacer |
MOA of class I anti-arrhythmics class II? class III? class Iv? | Na channel blockers B-blockers K channel blockers CCBs |
which drugs are in class Ia anti-arrythmics? | Quinidine Amiodarone Procainamide Disopyramide |
which drugs are in the class Ib anti-arrhythmics? | I Be with my Lid To Mex(ico) lidocaine tocainide mexiletine |
which drugs are in the class Ic anti-arrythmics? | See (C)! And Can't (EnCain) We FLEe if we PROP up PHENOMS? encainide flecainide propafenone |
MOA class IA anti-arrhythmics? | increased AP duration increased ERP increased QT interval |
uses for class IA anti-arrhythmics | atrial and ventricular arrhythmias (esp reentrant and ectopic) SVT and VT |
MOA for class IB anti-arrhythmics | decreases AP duration |
use for class IB anti-arrhythmics | acute ventricular arrhythmias, esp post MI |
MOA for class IC anti-arrhythmics | no effect on AP |
uses for class IC anti-arrhythmics | VT --> FV inretractable SVT LAST resort |
toxicity of quinidine | cinchonism (HA, tinnitus, thrombocytopenia, torsades de pointes from increased QT interval) |
toxiciyt of procainamide | SLE-like syndrome (reversible) |
toxicity of IB anti-arrhythmics? | local anesthetic CNS stimulation/depression CV depression |
toxicity of IC anti-arrhythmics | pro-arrhythmic (esp post-MI) prolongs refractory period |
receptor selectivity for epi? | all are equal |
receptor selectivity for NorE | a1 = a2 > b1 |
receptor selectivity for isoproteronol | B1=b2 |
receptor selectivity for DA | d1 = d2 > B > a |
receptor selectivity for dobutamine | b1 > b2 |
receptor selectivity for phenylephrine | a1 > a2 |
receptor selectivity for albuterol | b2 > b1 |
receptor selectivity for terbutaline | b2 > b1 |