extra pharma questions Flashcards
again, these aren't from past exams. (169 cards)
A patient comes into the ER who has been poisoned. What is the first course of action?
a. find out what the poison is so you know how to treat it
b. stabilize the patient
c. take a history
b. stabilize the patient
he may die by the time you think of the right poison
The lethal dose of Nicotine is 1mg/kg. How much Nicotine does it take to kill a 70kg person?
70mg
this question was done in class
Drugs that end with -lol are
a. alpha receptor antagonists
b. beta receptor antagonists
c. anesthetics
b. beta receptor antagonists
Drugs that end with -zosin are
a. alpha receptor antagonists
b. beta receptor antagonists
c. anesthetics
a. alpha receptor antagonists
Drugs that end with -caine are
a. alpha receptor antagonists
b. beta receptor antagonists
c. anesthetics
c. anesthetics
What are chelating agents?
an agent that binds to other substances to eliminate them from the body
For what type of drug can we use the dose-response curve?
a. graded response drugs
b. quantal response drugs
c. both
c. both
What is true about tachyphylaxis?
a. its a slow and gradual drug tolerance
b. increasing the dose will not help in reversing it
b. increasing the dose will not help in reversing it
What’s the difference between side effect and adverse effect?
side effects occur through the same pharmacological action of the drug, while an adverse effect occurs via different mechanisms
Which of the following is true?
a. ionized drugs can diffuse across cell membranes
b. acidic drugs are better absorbed in the intestine
c. basic drugs are better absorbed in the intestine
c. basic drugs are better absorbed in the intestine
What is true about absorption?
a. the faster the gastric emptying, the more is absorbed
b. the more P-glycoprotein expression, the less the absorbtion
c. surface area is inversely proportional to absorption
b. the more P-glycoprotein expression, the less the absorption
What would happen to a patient that has hypoalbuminemia when he takes the average recommended amount of a drug?
a. no effect
b. he needs more of the drug to compensate
c. toxicity
c. toxicity
Which of the following is true about renal drug excretion?
a. only ionized, water soluble drugs can be excreted
b. only nonionized, fat soluble drugs can be excreted
c. large, protein bound drugs are excreted
a. only ionized, water soluble drugs can be excreted
what occurs to drug metabolism when P450 enzyme degradation is reduced?
a. metabolism is inhibited
b. metabolism is induced
b. metabolism is enduced
Phase 1 of drug metabolism is done by
microsomal oxidases and cytochrome P450 enzyme system (CYP450)
Which of these doesn’t occur in phase 1?
a. oxidation
b. sulfication
c. reduction
d. hydrolysis
b. sulfication
occurs in phase 2
Which of the following is a has bidirectional filtration?
a. glomerulus
b. proximal convoluted tubule
c. distal convoluted tubule
b. proximal convoluted tubule
What occurs when the urine pH becomes lower (more acidic)?
a. more acidic stuff excreted
b. more basic stuff excreted
b. more basic stuff excreted
the basic drugs react to the acid, become ionized and can go out in urine form because it is water soluble
Which of the following is NOT saturable?
a. glomerulus
b. proximal convoluted tubule
c. distal convoluted tubule
a. glomerulus
Which is FALSE about hepatic excretion?
a. it works most efficiently when the molar weight is low
b. glucuronide is added to make things more excretable
c. drugs with a high extraction ratio are the most affected by the first pass effect
a. it works most efficiently when the molar weight is low
Which of the following reduce the half-life of a drug?
a. heart failure
b. C-P450 induction
c. C-P450 inhibition
b. C-P450 induction
Give an example of a substance that follows zero order kinetics
Alcohol
True/False: T1/2 (half-life) is inversely correlated to concentration
False; T1/2 is not affected by concentration
Which of the following is a false statement about steady-state concentration?
a. it takes four to five half-lives to reach
b. at steady state, the dosing rate and elimination rate are equal
c. you can reach steady state concentration faster if you increase infusion rate
c. when you increase infusion rate you can reach steady state concentration faster
(higher infusion rate just makes the steady state concentration higher)