Medical Physiology and Pharmacology
2025 EXAM QUESTIONS AND VERIFIED
ANSWERS (100% CORRECT ANSWERS)
A+ GRADED | ALREADY PASSED!!
which definition best describes a lead compound - Correct Ans-the first compound
discovered to have the desired activity
which method of discovering a drug is generally the least expensive - Correct Ans-
molecular docking
what is the name of the process that involves step-wise alteration of a drug to improve
its properties - Correct Ans-structure activity relationship
what was the estimated research and development expenses of pharma in 2016 -
Correct Ans-60 billion
which branch of pharmacology studies the effect of the body on drugs - Correct Ans-
pharmacokinetics
which branch of pharmacology studies how patients respond differently to drugs -
Correct Ans-pharmacogenetics
which branch of pharmacology studies the desired effect of drugs on the body, usually
at the molecular level - Correct Ans-pharmacodynamics
which branch of pharmacology studies adverse effects of drugs on the body - Correct
Ans-toxicology
which branch of pharmacology does excretion fall under - Correct Ans-
pharmacokinetics
which is the chemical name for a popular OTC pain killer - Correct Ans-N-acetyl-para-
aminophenol
which stage of translational research is the first to utilize a FDA approved drug - Correct
Ans-T3
the transition between which two phases of translational research involves switching
from controlled settings real-world setting - Correct Ans-T2-T3
PHYSIOLOGY
,PHYSIOLOGY
which type of drug is most likely to be given orally - Correct Ans-small molecule
overnight contact lenses are considered ? medical devices - Correct Ans-class III
which term describes the process of taking a piece of humor tumor from a patient and
placing it under the skin of a mouse in order to do pre-clinical testing - Correct Ans-
patient-derived xenograft
in order to do a clinical trial in humans, IRB approval must be obtained. From which
regulatory body must approval be obtained in order to carry out a similar study in rats? -
Correct Ans-IACUC
gaining information on which of the following is the primary purpose of a Phase I clinical
trial - Correct Ans-treatment safety
which of the following requires direct action by a patient (or their guardian) before they
can be enrolled in a phase I clinical trial - Correct Ans-informed consent
in which type of clinical trial is a MTD most likely to be determined - Correct Ans-phase
1
what government agency regulates phase I clinical trials in the US - Correct Ans-FDA
a clinical trial for the use of a new pain killer in terminal cancer patients who have been
admitted to hospice would be considered what type of clinical trial - Correct Ans-quality
of life trial
how many groups of patients would be required for a placebo-controlled factorial trial to
test combinations of three drugs - Correct Ans-8
in which type of clinical trial is every patient guaranteed to receive active drug - Correct
Ans-cross-over trial
exclusion criteria for a clinical trial for a new therapy for pediatric leukemia - Correct
Ans-patient is greater than 12 years old
the most common target of drugs is - Correct Ans-receptors
Gleevac targets - Correct Ans-enzymes
a diabetic receives an injection of insulin. Once the insulin reaches the pancreas, how
long do you expect it to take before a response can be measured - Correct Ans-minutes
a dose of agonist occupies 30% of receptors and gives an effect of 50. According to the
occupancy theory, what effect would you expect from a dose that occupies 90% of
receptors - Correct Ans-150
PHYSIOLOGY
,PHYSIOLOGY
most drugs bind in such a way that it is reversible without a chemical reaction. These
drugs must therefore lack which type of bond with their targets - Correct Ans-covalent
drug A requires 15 micromolar to reach 50% of its maximum response while drug B
requires 50 micromolar to reach 50% of its maximum response, which drug is more
potent - Correct Ans-drug A
drug A requires 15 micromolar to reach 50% of its maximum response while drug B
requires 50 micromolar to reach 50% of its maximum response, which drug is more
effective - Correct Ans-cannot tell
which term describes a molecule that produces an effect when binding a receptor but is
incapable of inducing 100% effect - Correct Ans-partial agonist
the addition of a competitive antagonist will affect the apparent ? of an agonist - Correct
Ans-potency
the addition of a non-competitive antagonist will affect the apparent ? of an agonist -
Correct Ans-efficacy
when drug A, an agonist, is given chronically, larger and larger concentrations are
needed in order to achieve the same effect. which phenomenon is likely occurring -
Correct Ans-desensitization
which type of response curve would you look at if you wanted to know the exact
response predicted in a controlled system at a specified drug concentration - Correct
Ans-graded concentration response
when developing a new drug, do you generally want a high or low therapeutic index -
Correct Ans-high
aspirin has an ED50=5mg/dl and a TD50=100mg/dl what is the therapeutic index of
aspirin - Correct Ans-20
through which routes of administration will at least some first-pass metabolism occur -
Correct Ans-oral, rectal
would you expect aspirin to be absorbed better at high or low pH - Correct Ans-low pH
would you expect a more polar or nonpolar drug to have more bioavailability - Correct
Ans-nonpolar
assuming the same lipophilicity and that all are neutrally charged which drug would you
expect to have the best membrane permeability - Correct Ans-tylenol
PHYSIOLOGY
, PHYSIOLOGY
which family of enzymes catalyzes the majority of phase I drug metabolism - Correct
Ans-CYPs
codeine undergoes which type of phase I metabolism reaction - Correct Ans-
dealkylation
tylenol undergoes which type of phase II metabolism reaction - Correct Ans-sulfation
the majority of drug excretion occurs in which organ - Correct Ans-kidney
biliary excretion occurs in which organ - Correct Ans-liver
imagine a drug with kEL=1.2 hr, clearance=14.4 L/hr, and Vd=12L/kg what loading dose
would be required to achieve a 2mg/L concentration in a 30kg patient - Correct Ans-720
after a single dose, a drugs concentration in the plasma is measured to be 10mg/L.
After one hour the plasma concentration is measured to be 5mg/L. How many hours will
it take for the plasma concentration to reach 0.02mg/L assuming first-order metabolism
- Correct Ans-9
imagine a drug with kEL=1.2 hr, clearance=14.4L/hr and Vd=12L/kg. Assuming constant
infusion of drug, roughly how long would it take for the drug concentration to reach
steady-state - Correct Ans-3 hr
imagine a drug with kEL=1.2 hr, clearance=14.4L/hr and Vd=12L/kg. In order to achieve
a steady-state plasma concentration of 2mg/L, how large should each maintenance
dose be if a 30kg patient is going to take an oral dose every 12 hours. - Correct Ans-
346 mg
a physician walks into a patient room and can immediately draw conclusions regarding
which one of the following sources of individuality in terms of drug response - Correct
Ans-condition or state of being
at which age would you expect a patient have the highest levels of P450 activity -
Correct Ans-50 years
prilosec is a substrate for P450 enzymes. Ingesting which of the following would likely
increase its metabolism - Correct Ans-grilled hotdog
genetics can influence which branch of pharmacology - Correct Ans-kinetics and
dynamics
which drug has an adverse interaction with Xanax - Correct Ans-indinavir
PHYSIOLOGY