| 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 |