Pharmacology Flashcards

1
Q

Loop diuretics

-ex, site of action, MOA

A

Ex: furosemide, ethacrynic acide, bumetanide, torsemide
Site of action: Loop of Henle
MOA: inhibits the Na/K/2Cl transporter, decreasing urine concentration and increasing calcium excretion
Loops lose calcium

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2
Q

Loop diuretics side effects

A
Ototoxicity
Hypokalemia
Hypocalcemia
Dehydration
Gout
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3
Q

Thiazide diuretics

-examples, site of action, MOA

A

Ex: HCTZ, chlorthalidone
Site of action: early distal tubule
MOA: Decreases NaCl reabsorption leading to decreased diluting capacity of nephron; decreases calcium excretion

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4
Q

Thiazide diuretics side effects

A
Hypokalemic metabolic alkalosis
Hyponatremia
HyperGLUC
-hyperglycemia
-hyperlipidemia
-hyperuricemia
-hypercalcemia
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5
Q

Potassium sparing diuretics

-Ex, Site of action, MOA

A

Ex: spironolactone, triamterene, amiloride
Site of action: cortical collecting tubule
MOA: spironolactone is an aldosterone inhibitor; the others block Na channels

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6
Q

Potassium sparing diuretics side effects

A

Hyperkalemia
Gynecomastia
Sexual dysfunction

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7
Q

Carbonic anhydrase inhibitors

-ex, site of action, MOA

A

Ex: acetazolamide
Site: proximal convoluted tubule
MOA: inhibits carbonic anhydrase; decreases total body HCO3

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8
Q

Carbonic anhydrase inhibitor side effects

A

Hyperchloremic metabolic acidosis
neuropathy
NH3 toxicity
Sulfa allergy

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9
Q

Osmotic agents

-ex, site of action, MOA

A

Ex: mannitol
Site: proximal tubule
MOA: increases tubular fluid osmolarity leading to increased urine flow

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10
Q

Mannitol side effects

A

Pulmonary edema
Dehydration
Contraindicated in anuria and CHF

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11
Q

HMG-CoA reductase inhibitors

-MOA, effect on lipids, side effects

A

aka statins
MOA: inhibits rate limiting step in cholesterol synthesis

Effect on lipids: decrease LDL and TG

SE: myositis, increase LFTs, warfarin potentiation

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12
Q

Fibrates

-MOA, effects, SE

A

ie gemfibrozil
MOA: increase lipoprotein lipase which increases VLDL and TG catabolism

Effects: decreases TG, increases HDL

Side effects: GI upset, cholelithiasis, myositis, increases LFTs

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13
Q

Cholesterol absorption inhibitors

-MOA, effects, SE

A

ie ezetimibe
MOA: decreases absorption of cholesterol and the small intestine brush border

Effects: decreases LDL

SE: diarrhea, abdominal pain, can cause angioedema

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14
Q

Niacin

-MOA, effects, SE

A

MOA: decreases fatty acid release from adipose tissue; decreases hepatic synthesis of LDL

Effects: increases HDL, decreases LDL

AE: skin flushing (prevented w/ ASA because its prostaglandin mediated), paresthesias, pruritis, GI upset, increased LFTs

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15
Q

Bile acid resins

-MOA, effects, SE

A

ex: cholestyramine

MOA: binds intestinal bile acids leading to decreased bile acid stores and increased catabolism of LDL from plasma

Effects: decreased LDL

SE: constipation, GI upset, LF abnormalities, myalgias; can decrease absorption of other drugs from the small intestine

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16
Q

SE of B-blockers

A

Impotence, fatigue, depression, CHF exacerbation, bradycardia, bronchospasm

17
Q

CCBs

A

Dihydropyridines: nifedipine, felodipine, amlodipine
Nondihydropyridines: verapamil, diltiazem

They vasodilate

18
Q

CCB SE

A

Dihydropyridines: peripheral edema, flushing, HA

Nondihydropyridines: orthostasis, hirsutism

19
Q

Hydralazine

A

Vasodilator that decreases peripheral resistance of the arteries/arterioles

SE: headache, SLE-like syndrome

20
Q

Methyldopa, clonidine

A

inhibitis SANS through a2 receptors

SE: somnolence, orthostatic hypotension, impotence, rebound HTN