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18 Cards in this Set
- Front
- Back
What does somatostatin (octreotide) do?
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blocks histamine release from ECL cell - preventing acid release from parietal cell
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what do muscarinic antagonists do to the gastric parietal cell?
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ex. atropine - inhibits the signaling (via Ach) to the parietal cell to release H+ - inhibits M3 receptor
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Bismuth, sucralfate MOA and use
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binds to ulcer base, providing physical protection, and allow HCO3- secretion to reestablish pH gradient in mucous layer
use: increase ulcer healing, traveler's diarrhea |
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what is triple therapy for?
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H.pylori ulcers
Metronidaozole, amoxicillin (or tetracycline), bismuth or could use PPI (-prazole) |
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Misoprostol MOA, use, toxicity
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A PGE1 analog. increased production and secretion of gastric mucous barrier, decreased acid production
use: prevention of NSAID induced peptic ulcers; maintenace of a PDA. used to induce labor toxicity: diarrhea, don't use in women that are pregnant (can cause abortion) |
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what do you use to keep open a PDA
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misoprostol
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What do muscarinic antagonists do in the gut? MOA, uses, toxicites
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Pirenzepine, propantheline
blocks M1 receptors on ECL cells (decrease histmaine secretion) and blocks M3 receptors on parietal cells (decreased H+ secretion) uses: peptic ulcer (rarely used) toxicity: tachycardia, dry mouth, difficulty focusing eyes |
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antacid use
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can affect absorption, bioavailability, or urinary excretion of other drugs by altering gastric and urinary pH or by delaying gastric emptying
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what are the problems associated with overuse of antacids? What do they all cause?
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All cause hypokalemia!
aluminum hydroxide overdose: constipation and hypophosphatemia; proximal muscle weakness, osteodystrophy, seizures (aluMINIMUM amount of feces) Magnesium hydroxide - diarrhea, hyporeflexia, hypotension, cardiac arrest (Mg = Must go to the bathroom) calcium carbonate - hypercalcemia, rebound acid increase (can chelate and decrease effectivenss of other drugs (tetracycline) |
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infliximab MOA, uses, toxicity
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monoclonal antibody against TNF, proinflammatory cytokine
use: crohn's disease, RA toxicity: respiratory infection (can reactivate latent TB), fever, hypotension |
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sulfasalazine MOA, use, toxicity
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MOA - combination of sulfapyridine (antibacerial) and 5-aminosalicylic acid (anti-inflammatory). activated by colonic bacteria
use: UC and crohn's disease toxicity: malaise, nausea, sulfonamide toxicity, reversible oligospermia |
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what drug causes reversible oligospermia?
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sulfasalzine - used for UC and crohn's disease
mix of antibacterial and antinflammatory |
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Ondansetron MOA, use, toxicity
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5-HT3 antatognist. powerful central acting antiemetic
use: control vomiting postop and in patients undergoing chemo toxicity: headache, constipation 'can go on dancing' |
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5-HT3 antagonist is what drug?
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odansetron - antiemetic
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Metoclopramide MOA, use, toxicity
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D2 receptor antagonist. increased resting tone, contractility, LES tone, motility. Does not influence colon transport time
use: diabetic and post surgery gastoparesis toxicity: increase parkinsonian effects. restlessnes, drowsiness, fatigue, depression, nausea, diarrhea. drug interaction with digoxin and diabetic agents. contraindicated in patients with small bowel obstruction |
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what patients can you not give metoclopramide to?
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patients with small bowel obstructions
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H2 blockers
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-tidine (cimentidine, ranitidine, famotidine, nizatidine)
reversibly block H2 receptors - decreased H+ release by parietal cells for gastric ulcers, gastritis, and mild GERD toxicity: inhibitor of P-450 has antiandrogenic effects (prolactin release, gynecomastia, impotence, decreased libido in males) |
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PPI's
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-prazole (omeprazole, lansoprazole)
irreversibly inhibit H+/K+ pump on parietal cells - inhibit H+ release use for peptic ulcers, gastritis, GERD, zollinger-ellison syndrome |