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PHM 520 Final Exam Practice Questions With Verified Answers

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PHM 520 Final Exam Practice Questions With Verified Answers What type of reactions are the most common cause of drug incompatibility and why? - answeracid-base reactions because precipitation of nonionized drug forms approximately how many commonly used drugs are incompatible or unstable when a...

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  • October 2, 2024
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  • 2024/2025
  • Exam (elaborations)
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  • PHM 520
  • PHM 520
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PHM 520 Final Exam Practice Questions
With Verified Answers


What type of reactions are the most common cause of drug incompatibility and why? -
answer✔acid-base reactions because precipitation of nonionized drug forms
approximately how many commonly used drugs are incompatible or unstable when added or
combined with usual fluids or agents?


a. 10%
b. 30%
c. 50%

d. 70% - answer✔b. 30%
an undesirable reaction occurring between a drug and a container, solution, or another drug is
called? - answer✔incompatibility

alteration of drug effect due to the influence of another substance is called? - answer✔drug
interactions

where do interactions occur? - answer✔inside the body

where does incompatibility occur? - answer✔in a fluid contianer or infusion line

are interactions or are incompatibilities visible? - answer✔incompatibilities
what type of incompatibility results from the modification of pharmacological effect from prior
concomitant administration of other drugs? - answer✔therapeutic incompatibilty
what mechanism of therapeutic incompatibility involves the effect of a drug on another from the
point of view of absorption, distribution, metabolism, and excretion? - answer✔pharmacokinetic
what mechanism of therapeutic incompatibility is related to pharmacological activity of the
interacting drugs such as synergism/antagonism? - answer✔pharmacodynamic

, ©BRAINBARTER 2024/2025


pharmacodynamic is what the _______ does to the _______ - answer✔drug, body

pharmacokinetic is what the _______ does to the ________ - answer✔body, drug
an interaction that results in change in color, odor, taste, viscosity, and morphology is what type
of incompatibility? - answer✔physical incompatibility

physical incompatibilities usually refer to? - answer✔precipitation or phase separation

what are factors responsible for physical incompatibility? - answer✔pH value and buffer
capacity, solubility and precipitation, complex formation, adsorption
what effect will ingestion of antacids over a period of 24 hours have on urinary pH? -
answer✔increase pH

are acidic drugs excreted faster or slower when urinary pH is alkaline? - answer✔faster
acidic drugs will diffuse back into the blood from the urine when the urine is acidic or alkaline? -
answer✔acidic
interactions between ionized drugs will form _______ with _______ charges -
answer✔complexes, reduced

cation-anion interactions result in? - answer✔formation of relatively insoluble precipitate

ion pair formation results in? - answer✔burying of charges
what is the interaction between a metal atom or ion and another species called? -
answer✔chelation

the attachment of a molecule to a surface is called? - answer✔adsorption
what type of incompatibility results in change in chemical properties of pharmaceutical dosage
form? - answer✔chemical incompatibility
hydrolysis, oxidation, reduction, racemization are types of what incompatibility? -
answer✔chemical
which types of solubilization methods use a means of entrapment?


a) complexation
b) micellar
c) hydrotrophy

, ©BRAINBARTER 2024/2025


d) a and b

e) all of the above - answer✔*d) a and b
which of the following expresses the number of moles of solute in 1 kg of solvent?


a) molarity (M)
b) molality (m)
c) normality (N)

d) mole fraction - answer✔*b) molality (m)


a is incorrect because molarity expresses the number of moles of solute in 1 liter of SOLUTION


c is wrong because it expresses the number of equivalents of solute in 1 liter of solution


d is wrong because it expresses the ratio of moles of constituent to total moles
driving force in drug movement in aqueous diffusion model:


a) active transport
b) facilitated transport
c) concentration gradient

d) all of the above - answer✔*c) concentration gradient
which are most likely to diffuse across membranes:


a) charged drugs
b) ionized drugs
c) polar drugs

d) non-ionized drugs - answer✔*d) non-ionized drugs

, ©BRAINBARTER 2024/2025


a, b, and c are all hydrophilic and are not as likely to cross the membrane since membrane
permeability favors more lipophilic drugs
which equation describes change in concentration with time at a specific location by taking into
account the cross sectional area and partition coefficient?


a) Fick's first law
b) Fick's second law
c) Noyes-Whitney law

d) angle of repose - answer✔*b) Fick's second law


a is incorrect because Fick's first law describes the amount of drug flowing through a unit area of
barrier in unit time, and doesn't take into account cross sectional area or partition coefficient


c is incorrect because it describes dissolution rate


d is incorrect because it describes flow properties of a powder
which solubilization process involves the use of cyclodextrin, which is an oligosaccharide with a
hydrophobic cavity?


a) complexation
b) hydrotrophy
c) pH adjustment

d) crystal modification - answer✔*a) complexation


b involves adding a large amount of a second solute to increase solubility


c is used to prevent precipitation of drug

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