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nonselective adrenergic agonist (protype)
epinephrine (Adrenalin)
epinephrine (onset)
immediate to 5 min
epinephrine (duration)
1 - 4 hours
epinephrine (indications)
CPR, anaphylaxis, local vasoconstriction, mydriasis
epinephrine (mechanism of action)
stimulates alpha and beta receptors
epinephrine (routes)
sub-q, IV, IM, inhalation, topical, ophthalmic
epinephrine (adverse effects)
nervousness, tremors, tachycardia, HTN, dysrhythmias, pulmonary edema, CNS stimulation, local necrosis
epinephrine (contraindications)
hypersensitivity, closed angle glaucoma, CAD
epinephrine (pregnancy)
category C
alpha 1 adrenergic agonists (protype)
phenylephrine (neo-synephrine)
phenylephrine (onset)
immediate to 1-2 hours
phenylephrine (duration of action)
15 min - 3 hours
phenylephrine (indications)
nasal congestion, hypotension
phenylephrine (mechanism of action)
activates alpha-1 receptors in the peripheral nervous system
phenylephrine (routes)
PO, sub-q, IM, IV, intranasal, ophthalmic
phenylephrine (adverse effects)
reflex tachycardia, decreased peripheral blood flow, CNS stimulation
phenylephrine (contraindications)
severe HTN, preexisting bradycardia, CAD, narrow angle glaucoma
phenylephrine (pregnancy)
category C
beta adrenergic agonist (protype)
isoproterenol (Isuprel)
isoproterenol (onset)
immediate to varies
isoproterenol (duration of action)
less than 1 hour to 12 hours
isoproterenol (indications)
increased myocardial contraction, transient heart block
isoproterenol (mechanism of action)
activates beta-1 and beta-2 receptors
isoproterenol (routes)
IV, PO, inhalation
isoproterenol (adverse effects)
dysrhythmias, CNS stimulation, headache, nausea, vomitting
isoproterenol (contraindications)
CAD, HTN, dysrhythmias, hyperthyroidism, diabetes
isoproterenol (pregnancy)
category C
thiazide diuretic (protype)
hydrochlorothiazide (Microzide)
hydrochlorothiazide (routes)
PO
hydrochlorothiazide (onset)
2 hrs; peak 4 hrs
hydrochlorothiazide (duration of action)
6-12 hours; half life 45-120 min
hydrochlorothiazide (indications)
HTN, ascites related to edema, heart failure, nephrotic syndrome
hydrochlorothiazide (mechanism of action)
acts on distal tubule to decrease reabsorption of sodium
hydrochlorothiazide (adverse effects)
hypotension, dizziness, headache, electrolyte imbalances, gout, blood dyscrasias
hydrochlorothiazide (contraindications)
hypersensitivity, anuria, jaundiced neonates
hydrochlorothiazide (pregnancy)
category B
loop diuretic (protype)
furosemide (Lasix)
furosemide (route)
PO, IV, IM
furosemide (onset)
PO: 30-60 min IV: 2 hrs IM: 4-8 hrs
furosemide (duration)
PO: 6-8 hrs IV: 2 hrs IM: 4-8 hrs
furosemide (indications)
acute edema, hypertension
furosemide (mechanism of action)
prevents reabsorption of sodium and chloride in loop of henle
furosemide (adverse effects)
orthostatic hypotension, syncope, tachycardia, dysrhythmias, nausea and vomiting, ototoxicity, gout, metabolic alkalosis, electrolyte abnormalities
furosemide (contraindications)
hypersensitivity, anuria
furosemide (pregnancy)
category C
potassium sparing diuretic (protype)
spironolactone (Aldactone)
spironolactone (route)
PO
spironolactone (onset)
2-3 days, up to 2 weeks for max effect
spironolactone (duration)
2-3 days, half life up to 24 hrs
spironolactone (indications)
mild hypertension, heart failure, nephrotic syndrome, liver disease
spironolactone (mechanism of action)
inhibits action of aldosterone in distal tubule and collecting ducts
spironolactone (adverse effects)
hyperkalemia
spironolactone (contraindications)
hyperkalemia, anuria
spironolactone (pregnancy)
category D
alpha 1 adrenergic antagonist (protype)
prazosin (Minipress)
prazosin (routes)
PO, IV, SQ
prazosin (onset)
2 hrs, varies
prazosin (duration)
less than 24 hours
prazosin (indications)
hypertension, BPH, reynaud’s, pheochromocytoma
prazosin (mechanism of action)
competes with norepinephrine at alpha 1 receptors on vascular smooth muscle
prazosin (adverse effects)
orthostatic hypotension, dizziness, drowsiness, fatigue, 1st dose phenomenon, erectile dysfunction
prazosin (contraindications)
sensitivity
caution: older, renal impairment, CAD
prazosin (pregnancy)
category C
beta adrenergic antagonist (protype)
propranolol (Inderal)
propranolol (route)
PO, IV
propranolol (onset)
PO: 1-2 hrs IV: immediate
propranolol (duration)
3-5 hrs
propranolol (indications)
hypertension, angina, dysrhythmias, migraine, prophylaxis, essential tremor (off label)
propranolol (mechanism of action)
block beta-1 receptors in heart and beta-2 receptors in lungs
propranolol (adverse effects)
bronchospasm, agranulocytosis, stevens-johnson syndrome, bradycardia, fatigue, impotence [rebound tachycardia, myocardial ischemia if abrupt withdrawal]
propranolol (contraindications)
cardiogenic shock, severe heart failure, bradycardia, COPD/asthma, diabetes
propranolol (pregnancy)
category C
beta 1 antagonist (protype)
metoprolol (Lopressor, Toprol)
metoprolol (route)
PO, IV
metoprolol (onset)
PO: 15 min IV: immediate
metoprolol (duration)
13-19 hrs
metoprolol (indications)
hypertension (not 1st line), chronic stable angina, stable heart failure, migraine prophylaxis, essential tremor, atrial dysrhythmias, acute MI
metoprolol (mechanism of action)
selective beta-1 antagonist at receptors in cardiac muscle
metoprolol (adverse effects)
complete heart block, dizziness, fatigue, bradycardia, agranulocytosis, rebound cardiac excitation
metoprolol (contraindications)
cardiac shock, severe bradycardia, heart block
metoprolol (pregnancy)
category C
calcium channel blocker types
dihydropyridines and nondihydropyridines
dihydropyridines (protype)
nifedipine (Adalat, Procardia)
nifedipine (route)
PO
nifedipine (onset)
30-60 min, 6 hr (extended release)
nifedipine (duration)
4-8 hrs, 24 hrs (extended release)
nifedipine (indications)
hypertension, chronic stable angina
nifedipine (mechanism of action)
blocks calcium channels in vascular smooth muscle, including coronary arteries
nifedipine (adverse effects)
hypotension, dizziness, headache, flushing, peripheral edema
nifedipine (contraindications)
hypersensitivity
nifedipine (pregnancy)
category C
nondihydropyridines (protype)
verapamil (Calan, Isoptin, Verelan)
verapamil (route)
PO, IV
verapamil (onset)
PO: 1-2 hrs IV: 1-5 min
verapamil (duration)
PO: 3-7 hrs, 24 hrs (extended release) IV: 2 hrs
verapamil (indications)
antidysrhythmic, hypertension, angina
verapamil (mechanism of action)
inhibits flow of calcium into cardiac muscle and vascular smooth muscle cells
verapamil (adverse effects)
worsening heart failure, bradycardia, reflex tachycardia, AV block, peripheral edema
verapamil (contraindications)
AV block, severe hypotension, SSS
verapamil (pregnancy)
category C