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Chapter_07:_Medicines_and_Pharmocology
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Published
07/07/2024
Drugs administered sublingually and rectally have higher bioavailability because they bypass the {{c1::liver}}
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Drug absorption through the skin is based on lipid solubility through the {{c1::epidermis}}
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Drugs absorbed through the CSF are {{c1::lipid}}-soluble
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Sulfonamides in newborns can displace bilirubin from albumin leading to {{c1::kernicterus}}
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Tetracyclines and heavy metals in the body tend to get stored in {{c1::bone}}
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A constant amount of drug being eliminated regardless of the dose present is {{c1::zero}} order kinetics
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Drug being eliminated proportional to the dose is {{c1::first}} order kinetics
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A drug reaches a steady state after {{c1::5}} half-lives
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The amount of drug in the body divided by the amount of drug in blood is known as the {{c1::volume of distribution (Vd)}}
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The fraction of unchanged drug reaching the systemic circulation after administration is known as {{c1::bioavailability}}
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The drug level at which a desired effect occurs in 50% of patients is known as {{c1::ED50}}
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The drug level at which death occurs in 50% of patients is known as {{c1::LD50}}
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The requirement of higher doses of a drug to produce a given response is known as {{c1::tolerance}}
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A rapid decrease in response after administration of a drug is known as {{c1::tachyphylaxis}}
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The maximum effect that a drug can produce is known as {{c1::efficacy}}
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The amount of drug needed to produce a given effect is known as {{c1::potency}}
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Demethylation, oxidation, reduction, and hydrolysis reactions are all a part of phase {{c1::I}} drug metabolism
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Attaching glucuronic acid or sulfates forming water-soluble metabolites is phase {{c1::II}} drug metabolism
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The most important organ for eliminating most drugs is the {{c1::kidney}}
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{{c1::Water}} soluble dugs are more likely to eliminated in an unaltered form
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{{c1::Fat}} soluble dugs are more likely to metabolized prior to elimination
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Gout is caused by the buildup of {{c1::uric acid}} crystals
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Gout affecting the 1st metatarsophalangeal joint is known as {{c1::podagra}}
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A gout drug that blocks inflammation by binding tubulin and inhibiting cell migration is {{c1::colchicine}}
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The NSAIDs of choice for gout are {{c1::naproxen}} and {{c1::indomethacin}}
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A gout drug that works by inhibiting {{c1::xanthine oxidase}} is allopurinol
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A gout drug that works by increasing renal secretion of uric acid is {{c1::probenecid}}
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A bile acid binding resin that works by decreasing the amount of bile acid resorption in the gut is {{c1::cholestyramine}}
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A prokinetic drug used for nausea that inhibits dopamine receptors is {{c1::metoclopramide}}
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Reglan is a brand name for {{c1::metoclopramide}}
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A macrolide antibiotic that can act as a prokinetic via activating the motilin receptor is {{c1::erythromycin}}
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A prokinetic drug that acts as an antagonist to the mu-opioid receptor is {{c1::alvimopan}}
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Entereg is a brand name for {{c1::alvimopan}}
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Loperamide slows gut motility by acting as a mu-opioid receptor {{c1::agonist}}
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Lomotil is a brand name for {{c1::diphenoxylate/atropine}}
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A first generation anti-histamine drug that can be used as an anti-emetic is {{c1::promethazine}}
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Phenergan is a brand name for {{c1::promethazine}}
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An antiemetic drug that works by inhibiting serotonin receptors is {{c1::ondansetron}}
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Digoxin can cause blood flow to the intestines to {{c1::decrease}}(increase or decrease)
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Is digoxin cleared with dialysis?{{c1::No}}
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An anti-arrhythmic drug that can cause pulmonary fibrosis or hyper/hypothyroidism is {{c1::amiodarone}}
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The treatment for torsades de pointes is {{c1::magnesium}}
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The drug class that acts as the best single agent to improve survival in patients with CHF is {{c1::ACE inhibitors}}
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The drug class that acts as the best single agent to improve survival in patients after myocardial infarction is {{c1::beta-b…
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Atropine administration causes the heart rate to {{c1::increase}}(increase or decrease)
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A drug that acts as a GnRH analogue is {{c1::leuprolide}}
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Flomax is a brand name for {{c1::tamsulosin}}
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NSAIDs inhibit prostaglandin synthesis, which leads to {{c1::decreased}} gastric mucus and HCO3- secretion(increased or decreased)
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NSAIDs inhibit prostaglandin synthesis, which leads to {{c1::increased}} acid production(increased or decreased)
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NSAIDs inhibit prostaglandin synthesis, which leads to {{c1::decreased}} renal perfusion(increased or decreased)
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An NSAID that acts as a selective COX-2 inhibitor is {{c1::celecoxib}}
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A PGE1 derivative drug that is used to prevent peptic ulcer disease is {{c1::misoprostol}}
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Haldol is a brand name for {{c1::haloperidol}}
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Lasix is a brand name for {{c1::furosemide}}
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A side effect of loop diuretics is metabolic {{c1::alkalosis}}(acidosis or alkalosis)
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A side effect of potassium sparing diuretics is metabolic {{c1::acidosis}}(acidosis or alkalosis)
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Remicade is a brand name for {{c1::infliximab}}
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The early stages of aspirin poisoning are characterized by {{c1::respiratory alkalosis}}(acid/base imbalance)
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The late stages of aspirin poisoning are characterized by {{c1::metabolic acidosis}}(acid/base imbalance)
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Use of gadolinium should be avoided in patients with {{c1::renal insufficiency}}
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Nephrogenic systemic fibrosis is a severe side effect of {{c1::gadolinium}} exposure in patients with renal insufficiency
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The most common side effect of iodine contrast is {{c1::nausea}}
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The most common side effect of iodine contrast that requires medical treatment is {{c1::dyspnea}}
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07/07/2024
The medical treatment of acetaminophen overdose is {{c1::N-acetylcysteine}}
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