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PHM 520 Final Exam Practice Actual Questions And Verified Detailed Answers

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PHM 520 Final Exam Practice Actual Questions And Verified Detailed Answers...

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PHM 520 Final Exam Practice Actual Questions And
Verified Detailed 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



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

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



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

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