Pharmacology Flashcards

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1
Q

Stool softeners

A

Docusate

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2
Q

Bulk-forming laxatives

A

Psyllium, methylcellulose

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3
Q

Irritant (stimulant) laxatives

A

Castor oil, bisacodyl, senna

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4
Q

Lubricating laxatives

A

Mineral oil, glycerin

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5
Q

Osmotic agents (laxatives)

A

magnesium hydroxide, magnesium citrate, sorbitol, lactulose, polyethylene glycol

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6
Q

Ocreotide- MOA and uses

A

Somatostatin analog that inhibits the release of vasodilatory hormones, causing splanchnic vasoconstriction; used for variceal bleeding, acromegaly, diarrhea (in endocrine disorders)

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7
Q

Dobutamine- MOA and uses

A

Inotrope that agonizes beta-1 receptors; used for maintenance of cardiac output

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8
Q

Metoclopramide- MOA, uses, major ADR

A

Primarily D2 antagonist, with some 5-HT3 antagonism and 5-HT4 agonism; antiemetic, promotes motility. May cause tardive dyskinesia.

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9
Q

Misoprostol- MOA, uses

A

Prostaglandin E1 derivative; used to prevent peptic ulcers and to induce uterine contractions in pregnant women

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10
Q

Omeprazole- MOA, uses

A

PPi; stomach ulcers

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11
Q

Tranexamic acid- MOA, uses

A

Inhibits multiple plasminogen binding sites; used for dental bleeding prophylaxis in hemophilia patients

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12
Q

Phytonadione- MOA, uses

A

Vitamin K; hypoprothrombinemia and warfarin stabilization

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13
Q

Digoxin- MOA, uses

A

Cardiac glycoside that directly inhibits Na+/K+ ATPase, indirectly inhibiting the Na+/Ca2+ exchanger to cause increased intracellular calcium and positive inotropy; used for heart failure and Afib (slows heart rate and increases vagal activity)

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14
Q

Digoxin- ADRs

A

Nausea/vomiting, diarrhea, yellow/green visual distortion, xanthopsia, hyperkalemia

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15
Q

Digoxin- risk factors for toxicity and treatment

A

Renal failure, drug interactions (verapamil, quinidine, amiodarone), and hypokalemia (increases digoxin binding); give anti-digoxin Fab frgaments

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16
Q

Milrinone- MOA, uses

A

Phosphodiesterase inhibitor, increasing cAMP and PKA and Ca2+ influx into cardiac cell, causing inotropy; short term IV treatment for acute decompensated heart failure

17
Q

Diltiazem- MOA, uses

A

L-type calcium channel blocker affecting smooth muscle to decrease peripheral vascular resistance, dilate coronary arteries, and prolong the AV node refractory period; used for hypertension, chronic stable angina, and supraventricular tachycardia

18
Q

Pilocarpine- MOA, uses

A

Cholinomimetic that slows heart rate by decreasing AV conduction velocity

19
Q

Procainamide- MOA, uses

A

Class 1A sodium channel blocker that decreases the slope of phase 0 of the action potential; antiarrhythmic

20
Q

Sucralfate- MOA, uses

A

Sulfated polysaccharide complexed to aluminum hydroxide, its strong negative charge binds to positively-charged proteins at base of ulcer, where it polymerizes to form a barrier, also stimulates angiogenesis; used for stomach/duodenal ulcers

21
Q

H2 antagonists

A

Cimetidine, rainitidine, nizatidine, famotidine

22
Q

Perchlorperazine- MOA, uses, ADRs

A

D2R agonist; antiemetic and anxiolytic (nonpsychotic); may cause neuroleptic malignant syndrome or extrapyramidal symptoms

23
Q

Dronabinol- MOA, uses

A

Cannadbinoid agonist; antiemetic and appetite stimulant for cancer patients

24
Q

Meclizine- MOA, uses

A

H1 agonist; motion sickness, vertigo

25
Q

Megestrol- MOA, uses, ADRs

A

Progestational agent; appetite-stimulant for cachexia, may cause thromboembolism, thrombophlabitis, adrenal suppression, cardiomyopathy