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Advanced Pharmacology Exam 1 questions with verified answers

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This exam tests knowledge on pharmacology topics

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Advanced Pharmacology Exam 1 Test With d d d d d d




Verified Solutions d




Once you graduate from an NP program, in order to prescribe you'll need: -
d d d d d d d d d d d d d d




d d d d d d d d d d d -Advanced nurse prescriber license d d d




-DEA # d




What is the purpose of a DEA #? -
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d d d d d d d d d d d Needed to prescribed scheduled drugs
d d d d




Rules for prescribing Schedule II drugs: -
d d d d d d d




d d d d d d d d d d d -Written script needed d d




-1 month supply only
d d d d




-No refills d




What is the PDMP? - d d d d d




d d d d d d d d d d d Prescription Drug Monitoring Program d d d




Used to effectively track patient's controlled substance uses across different health facilities (in the
d d d d d d d d d d d d d d



same state) d




What are clinical practice guidelines? -
d d d d d d




Recommendations that are intended to optimize patient care that are informed by a
d d d d d d d d d d d d d d d d d d d d d d d d



systematic review of the evidence and an assessment of the benefits/harms of alternative care
d d d d d d d d d d d d d d



practices



Ex: sepsis, CAP
d d




Common causes of medication errors: -
d d d d d d




d d d d d d d d d d d -Illegible writing d




-Drug names that sound alike
d d d d




1|Page

,-Medications that look alike d d d




-Administering a drug with the wrong route d d d d d d




What is pharmacokinetics? What are its 4 categories? -
d d d d d d d d d




d d d d d d d d d d d What the body does to the drug
d d d d d d




1. Absorption
d




2. Metabolism
d




3. Distribution
d




4. Excretion
d




Quickest route of absorption? Slowest? -
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d d d d d d d d d d d IV = quickest
d d d




IM = slowest
d d




What is the most common way drugs pass through cell membranes? -
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d d d d d d d d d d d Passive diffusion d




What characteristics of a drug allow it to pass most quickly through cell membranes (usually
d d d d d d d d d d d d d d d



through passive diffusion)? -d d d d




d d d d d d d d d d d Small, uncharged (unionized), lipid soluble--pass through membrane without any energy
d d d d d d d d d




What does it mean when a drug is ionized? -
d d d d d d d d d d




It means that the drug is stuck in the compartment it was ionized in and has to be moved to
d d d d d d d d d d d d d d d d d d d d d d d d d d d d d d



d the next compartment (cannot be absorbed into the bloodstream)
d d d d d d d d




Where do weak acids absorb? -
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d d d d d d d d d d d Stomach



Where do weak bases absorb? -
d d d d d d




d d d d d d d d d d d Small intestine d




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,pH of stomach: -
d d d d




d d d d d d d d d d d 2-4



pH of small intestine: -
d d d d d




d d d d d d d d d d d 6-7



pH of large intestine: -
d d d d d




d d d d d d d d d d d 6-7



pH of bloodstream: -
d d d d




d d d d d d d d d d d 7.35-7.45



pH of bladder: -
d d d d




d d d d d d d d d d d 5-8



pH of breastmilk: -
d d d d




d d d d d d d d d d d 7.1



Where will a drug absorb if it is a weak base that ionizes at a pH of 4 and lower? -
d d d d d d d d d d d d d d d d d d d d d




In the small intestine (since the stomach has a pH of 2-4, so the drug will become ionized
d d d d d d d d d d d d d d d d d d d d d d d d d d d d d



and move to the small intestine where it will be able to absorb into the bloodstream)
d d d d d d d d d d d d d d d




How can we manipulate the urine pH in cases of overdose? -
d d d d d d d d d d d d




d d d d d d d d d d d Drugs that are weak acids (aspirin) can be trapped and excreted through the urine.
d d d d d d d d d d d d d d




We raise pH of the urine (with sodium bicarb) to force the drug to ionize and allow it to be
d d d d d d d d d d d d d d d d d d d d



excreted, not reabsorbed through the bloodstream.
d d d d d




What is distribution? - d d d d




d d d d d d d d d d d How a drug will be transported to the tissues it needs to go to in order for it to exert its
d d d d d d d d d d d d d d d d d d d d d



effects




3|Page

, Drug factors related to distribution: -
d d d d d d




d d d d d d d d d d d -Lipid solubility d d




-Molecular size d




-Degree of ionization d d d




-Duration of action d d




-Cellular binding d




-Therapeutic effects d d




-Toxic effects d




(lipid soluble, small, and non-ionized drugs will distribute more quickly)
d d d d d d d d d




Body factors related to distribution: -
d d d d d d




d d d d d d d d d d d -Vascularity (poor perfusion, disruption of blood flow due to trauma--difficulty distributing)
d d d d d d d d d d




-Blood barriers (blood-brain-barrier can be problematic if we need to get drugs to the brain--will
d d d d d d d d d d d d d d d



need very high dosing since only a small amount of the drug will get through)
d d d d d d d d d d d d d d




-Transport mechanisms d d




-Plasma binding proteins d d d




-Disease states d




-Volume of distribution d d




-Drug interactions d




What is the key plasma protein involved with protein binding for medications? -
d d d d d d d d d d d d d




d d d d d d d d d d d Albumin



Why do we monitor albumin? -
d d d d d d




Indicative of nutritional status and how well protein-bound drugs will be transported to their
d d d d d d d d d d d d d d d d d d d d d d d d



d target locations d




What happens to the therapeutic effect of a drug when the patient is elderly and has very low
d d d d d d d d d d d d d d d d d d



levels of albumin? - d d d d




The drug does not bind to the protein (albumin) as much as expected, so there is a lot of
d d d d d d d d d d d d d d d d d d d d d d d d d d d d d d



free drug floating in the plasma; high risk for drug toxicity
d d d d d d d d d d




4|Page
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