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TEST BANK FOR PHARMACOTHERAPY ACTUAL EXAM 2025 WITH COMPLETE QUESTIONS AND ANSWERS RATED A+

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TEST BANK FOR PHARMACOTHERAPY ACTUAL EXAM 2025 WITH COMPLETE QUESTIONS AND ANSWERS RATED A+

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TEST BANK FOR PHARMACOTHERAPY
ACTUAL EXAM 2025 WITH COMPLETE
QUESTIONS AND ANSWERS RATED A+

The PH (for the COOH group) of each of the three drugs is as follows: thyroxine = 3.0,mesothyroxine =
4.0,neothyroxine = 5.0. Of these, which will be absorbed to the greatest extent from the stomach (pH =
1.0)
ANSWER-Neothyroxine




The multi drug resistance proteins (or p-glycoproteins) can protect liver and kidney cells by exporting
harmful chemicals against a concentration gradient in an energy-dependent manner. What is this
called?

ANSWER-active transport




Phase II conjugates typically have the following property/properties

ANSWER-rapidly excreted in the urine




A drug with a half-life of 2 hours is administered by continuous intravenous infusion. How long will it
take for the drug to reach 50% of its steady state concentration?

ANSWER-2 hours

,We have an expert-written solution to this problem!

Caffeine is eliminated primarily by metabolism and with first order kinetics. The half-life of caffeine
varies significantly with individuals, but is on average 5.0 hours. The volume of distribution is 0.60 L/kg.
Joe has a mass of 70 kg and is an average subject with regard to caffeine pharmacokinetics. He has a
regular habit of consuming a cup of coffee (85 mg of caffeine) at 8 am.

What is the clearance value (CL) of caffeine in a normal individual?

ANSWER-0.083 L/hr/kg




Which of the following routes is most likely to be affected by the first-pass effect?

ANSWER-oral




A drug, given as a 150 mg single dose, results in a peak plasma concentration of 10 ug/mL. The apparent
volume of distribution is (rapid distribution and negligible elimination prior to measuring the peak
plasma level):

ANSWER-15 L




Which of the following are routes of drug clearance?

-renal

-sweat

-intestines

ANSWER-all of the above

,What factor(s) may reduce drug bioavailability?

-gastric acid instability

-first-pass affect

-exposure to digestive enzymes

ANSWER-all of the above




What type of receptor is the muscarinic receptor?

ANSWER-G-protein coupled receptor




For a cholinesterase modified by an organophosphate compound (e.g. soman), what is the time-
dependent dealkylation process called yielding an enzyme refractory toward reactivation?

ANSWER-aging




Muscarinic receptors bind

ANSWER-acetylcholine




Which of the following is a clinical use for a muscarinic agonist?

ANSWER-"switching on" the urinary tract after surgery

, Indirect cholinergic agonists cause

ANSWER-inhibition of acetylcholinesterase and a corresponding increase in the synaptic acetylcholine
levels




Which of the following is characteristic of the sympathetic nervous system?

ANSWER-responded predominate during physical activity or when experiencing fright




A patient with an acute attack of glaucoma is treated with pilocarpine. The primary reason for its
effectiveness in this condition is its:

ANSWER-ability to lower intraocular pressure




Put the following steps in the correct order for neurotransmission at the cholinergic neuron

ANSWER-1. acetylcholine is synthesized from choline and acetyl-CoA

2. acetylcholine is released from storage vesicles into the synaptic cleft

3. acetylcholine is synthesized from choline and acetyl-CoA

4. acetylcholine is degraded by acetylcholinesterase




The autonomic nervous system innervates all of these except

ANSWER-skeletal muscle

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