| Term 
 | Definition 
 
        | GABA enhancer, intermediate time to sedation if given IV |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | GABA enhancer, extremely fast time to sedation if given IV |  | 
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        | Term 
 | Definition 
 
        | GABA enhancer, slow acting, but long lasting, sedation if given IV |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Acetylcholinesterase inhibitor, can enter the brain, but it is not used for brain disorders |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Acetylcholinesterase inhibitor, can't enter the brain |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Muscarinic and nicotinic receptor agonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Acetylcholinesterase inhibitor, short duration of action, reverses muscle paralysis in anesthesia |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Irreversible acetylcholinesterase inhibitor, can be used for glaucoma |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Irreversible acetylcholinesterase inhibitor, no medical use |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Muscarinic agonist, for GI motility |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Muscarinic agonist, glaucoma treatment |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Muscarinic agonist, from mushrooms |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Increases heart rate and blood pressure, nicotinic agonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Muscarinic antagonist, increases heart rate, causes dry mouth |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Nicotinic antagonist at the neuromuscular junction |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Nicotinic antagonist at the ganglia |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Nucleophile to break sarin bond to acetylcholinesterase |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Acetylcholinesterase inhibitor, site of action is the brain |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Alpha 1, Alpha 2, Beta 1, Beta 2 agonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Alpha 1, Alpha 2, Beta 1 agonist |  | 
        |  | 
        
        | Term 
 | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | Alpha 1 agonist, leading to increase in blood pressure and reflexive decrease in heart rate |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Competitive alpha 1 and alpha 2 antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Tyrosine hydroxylase inhibitor, blocks all catecholamine synthesis in CNS and periphery |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Increases dopamine production, used to treat Parkinson's Disease |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Alpha 2 agonist used to decrease blood pressure in an oral formulation |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Increaes the release of norepinephrine, but is normally metabolized quickly by MAO. Only significant if MAO is inhibited |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Catecholamine reuptake inhibitor, increases norepinephrine release by reversing the reuptake pump |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Increases release of norepinephrine, weak agonist of alpha 1, beta 1, beta 2. Used as a decongestant |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Catecholamine reuptake inhibitor, local anesthetic properties |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Selectively inhibits norepinephrine reuptake |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Non-selective MAO inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Selective MAO-B inhibitor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Phosphodiesterase inhibitor that can increase cardiac stimulation leading to arrhythmias, and can increase CNS excitation leading to convulsions. Used to treat apnea in infants. |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Phosphodiesterase inhibitor that increases cyclic GMP to relax vascular smooth muscle |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Low dose dilates renal vasculature, higher dose causes cardiac stimulation, highest dose causes overall vasoconstriction. Used to increase cardiac output while preserving renal function. |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Beta 1>beta 2 with some alpha 1 agonist activity. Beta 1 allows selective increase in force of cardiac contraction, inotropic effect>chronotropic effect |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Beta 2 agonist for bronchodilation |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Beta 2 agonist to prevent premature labor |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Noncompetitive alpha 1 and alpha 2 antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Alpha 1 antagonist, side effect of orthostatic hypertension on first dose |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Alpha 1A antagonist, for BPH treatment |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Competitive alpha 2 antagonist, produces CNS effects, also used as an aphrodisiac |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Beta 1 and beta 2 antagonist |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Beta 1 antagonist, provide exercise tolerance, better recovery from hypoglycemic episodes |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Beta  blocker with intrinsic sympathomimetic activity, blocks increase in heat rate and cardiac output |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Beta and alpha antagonist with anti-oxidant and antiproliferative activity. Reduces morbidity and mortality in patients with moderate heart failure |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Beta and alpha antagonist used for hypertension in pregnancy |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | prevents vesicular storage of catecholamines to lower blood pressure, but causes depression as a side effect |  | 
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