A) Acidic drugs
B) Neutral drugs
C) Basic drugs
D) pH has no affect on absorption
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Multiple Choice
A) Urinary pH does not affect renal excretion of drugs.
B) Urinary pH can be manipulated to facilitate drug excretion.
C) In alkaline urine,acidic drugs are more readily ionized.
D) Ionized substances are more soluble in water and thus they are easily excreted in urine.Chapter 2.An Introduction to Pharmacodynamics and Pharmacokinetics
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Multiple Choice
A) Chemical name.
B) Generic name.
C) Trade name.
D) Clinical name.
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Multiple Choice
A) Ionic bonding.
B) Van der Waals bonding.
C) Hydrogen bonding.
D) Compound bonding.
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Multiple Choice
A) Extraction ratio
B) First pass
C) Bioavailability
D) Solubility
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Multiple Choice
A) Tubular secretion is the way in which most drugs are removed by the kidneys.
B) Renal blood flow does not affect excretion of drugs.
C) Large-molecular-weight drugs,such as heparin,are easily filtered by the glomeruli.
D) Drugs that are tightly bound to plasma protein are readily filtered by the glomeruli.
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Multiple Choice
A) Poor metabolizers of clopidogrel do not efficiently convert it to its active form and thus may not receive its benefits.
B) Poor metabolizers may not metabolize clopidogrel and may instead develop toxic effects at therapeutic dosages.
C) The effects of clopidogrel are not changed in poor metabolizers.
D) Poor metabolizers require lower doses of clopidogrel in order to avoid toxic effects.
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Multiple Choice
A) Ability of a drug to permeate capillaries
B) First-pass effect
C) A drugs ability to bind to plasma proteins
D) Fat- or water-soluble characteristics
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Multiple Choice
A) salmeterol (Serevent)
B) norepinephrine
C) propanolol
D) albuterol (Proventil)
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Multiple Choice
A) Is not bound to its specific receptors.
B) Is not bound to plasma proteins.
C) Cannot exert a pharmacologic effect.
D) Has been dissolved from its tablet state.
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Multiple Choice
A) Chemical name.
B) Generic name.
C) Trade name.
D) Brand name.
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Multiple Choice
A) Ion channel
B) Nuclear receptors
C) G-protein receptor complex
D) Second messenger systems
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Multiple Choice
A) pH has no affect on drug absorption.
B) Increased blood flow to the gastrointestinal tract decreases absorption of orally administered drugs.
C) The solubility of drugs affects their absorption.
D) Absorption is not proportional to the surface area available.
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Multiple Choice
A) Absorption
B) Distribution
C) Tachyphylaxis
D) Metabolism
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Multiple Choice
A) Liver.
B) Small intestine.
C) Skin.
D) Kidney.
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Multiple Choice
A) Lower doses are needed to keep the active compounds working.
B) Higher doses are needed to keep the active compounds working.
C) No dosing changes need to be made for this medication.
D) Clearance rate has nothing to do with dosing medications.
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Multiple Choice
A) Metabolic induction effect.
B) Enzyme saturation effect.
C) Steady state effect.
D) First-pass effect.
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Multiple Choice
A) Antagonists produce their effect by changing the receptor.
B) Antagonists bind and block the effect of an endogenous agonist.
C) Antagonists have an affinity for activating cell receptors.
D) Antagonists induce the same response produced by the endogenous substance.
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