Ch. 7 Pharmacological Principles Flashcards
pharmacokinetics:
what the body does to drugs
-absorption
-distribution
-metabolism
-excretion
pharmacodynamics:
what the drug does to the body
-target sites for drug actions include receptors, ion channels, enzymes, and carrier proteins
method and rate at which drugs leave the site of administration:
a. absorption b. distribution c. metabolism d. excretion
a. absorption
for oral medications, absorption normally occurs in ________ and then in the _____
small intestine and then in the liver
occurs after the drug leaves the systemic circulation and enters the interstitium and cells:
a. absorption b. distribution c. metabolism d. excretion
b. distribution
drugs are redistributed in organs according to their ____ and ____ content
fat and protein content
True or False: most psychotropic drugs are lipophilic and highly protein bound
True
True or False: only the bound portion of the drug is active
False, only the unbound (free) portion is active
-those w/ low protein (albumin) levels may experience toxicity
process by which the drug becomes chemically altered in the body:
a. absorption b. distribution c. metabolism d. excretion
c. metabolism
First-pass metabolism= process in which drug is metabolized by:
a. blood brain barrier b. cytochrome P450 enzymes c. kidneys d. adrenal glands
b. cytochrome P450 enzymes
-in the liver and intestines prior to systemic circulation
process by which the drug is removed from the body:
a. absorption b. distribution c. metabolism d. excretion
d. excretion
Half-life (T1/2)= time needed to clear _____% of the drug from the plamsa
50%
-determines dosing interval and length of time to reach stead state
steady state: dose at which amount of drug _____ between doses is approximately equal to dose ______
-eliminated
-administered
True or False: drugs are usually administered one every half-life to achieve a steady state
True
How many half-lives does it take to achieve steady state or to completely eliminate the drug
5 half-lives
Enzyme inducers (increase or decrease?) the serum level of other drugs that are substrates of that enzyme- and cause ______ levels
-decrease
-cause subtherapeutic levels
Enzyme inhibitors (increase or decrease?) the serum level of other drugs that are substrates of that enzyme- and cause ______ levels
-increase
-cause toxic levels
Approx. 10% of Caucasians are poor metabolizers of the P450 ____ enzyme
2D6
Approx. 20% of Asians may have reduced activity of the P450 ____ enzyme
2C19
Which of these medications is considered an inducer of cytochrome P450?
a. Buproprion b. Clomipramine
c. SSRIs d. Carbamazepine
d. Carbamazepine
-the other meds listed are inhibitors
-more inhibitors include: Cimetidine, Clarithromycin, Fluoroquinolones, Grapefruit/ grapefruit juice, Ketoconazole
Which of these medications is an inhibitor of cytochrome P450?
a. Hypericum (St. John’s Wort) b. Phenytoin c. Nefazodone d. Phenobarbital
c. Nefazodone
-the other meds are inducers
-tobacco is also an inducer
liver disease may result in (toxic or subtherapeutic?) drug levels
toxic
True or False: drugs that reduce renal clearance (NSAIDs) may increase serum concentrations of drugs that are excreted by the kidneys (lithium)
True
True or False: older adults tend to have less body fat and more protein
False, they are more likely to have more body fat and less protein, making them more like to develop toxicity d/t accumulation and erratic blood levels of drug