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