Pharmacology: Acid, pro-kinetics, anti-emetics Flashcards

1
Q

metoclopramide moa

A

inhibit D2 receptor, releases brake on ACh, more is released causes increased contraction and motility

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2
Q

meto toxicities

A

short term: acute dystonia
long term: tardive dyskinesia
(involuntary repetitive movements, known as extrapyramidal Sx)

hyperprolactinemia

anxiety and depression

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3
Q

cause of meto hyperprolactinemia

A

inhibition of central dopa pathway- tuberoinfundibular pathway and affect pituitary

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4
Q

cause of meto EPS

A

inhibition of dopa nigrostriatal pathway, substantia nigra, dorsal striatum

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5
Q

cause of meto anxiety/ depression

A

affects dopa, serotonin, NE pathways in brain

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6
Q

erythromycin moa

A

motilin receptor agonist

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7
Q

PK issues w/ erythromycin

A

tachyphylaxis after 10-14 days

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8
Q

bethanechol moa

A

cholinergic agonist for motility, parasympathetic side effects when non selective

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9
Q

neostigmine moa

A

inhibits AChEsterase, more ACh and contraction/ motility

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10
Q

neostigmine toxicities

A

significant for cardiac- low CO, brady, AV block, cardiac arrest

need to keep atropine ready

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11
Q

sucralfate indications

A

GERD during pregnancy

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12
Q

moa of sucralfate

A

polymerizes at low pH, coats and protects mucosal layer

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13
Q

antacid moa

A

carbonates and hydroxides can neutralize stomach acid

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14
Q

antacid toxicities

A

met alkalosis, mostly w/ NaHCO3

diarrhea (Mg) or constipation (Al), can be combined to offset

hypophosphatemia, can form phosphate salts that prevent absorption and create gradient to pull phosphate into gut

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15
Q

4 antihistamine examples and moa for GERD

A

cimetidine, ranitidine, famotidine, nizatidine

inhibit histamine induced acid secretion by inhibiting H2 receptor on parietal cell

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16
Q

PK/PD issues for antihistamines

A

do not cross BBB

tolerance develops due to compensation by other pathways (gastrin, ACh)

17
Q

antihistamine drug interaction

A

inhibits multiple CYPs- increases effecive dose of warfarin, OCPs, theophylline (easily becomes toxic w/ CYP interaction)

reduces dose of clopiogrel

18
Q

PPIs moa

A

irreversible antagonist of K/H pump in parietal cells- absorbed in blood stream then released thru cells rather than direct effect via lumen

19
Q

PPI toxicities

A

C diff

hypomagnesia

B12 malabsorption

AIN

20
Q

PPI PK issues

A

pH trapping drives PPIs into cell and out

lower pH from blood to cytosol to secretory canaliculus (lumen of stomach)

21
Q

misoprostol indications

A

NSAID induced ulcers

22
Q

misoprostol moa

A

PGE2 analogue, inhibits gastric acid secretion

23
Q

misoprostol toxicities

A

category X for pregnancy, used in tandem w/ mifepristone to induce abortion

24
Q

odansetron moa

A

antagonize serotonin 5HT receptor, anti emetic

25
Q

odansetron toxicities

A

headache, dizzy, constipated, prolonged QT

26
Q

prochlorperazine, promethazine moa

A

D2 receptor antagonist, anti emetic

27
Q

prochlorperazine/ promethazine toxicities

A

EPS syndromes

prolonged QT