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Therapeutic Drug Markers

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Total cards: 24•Content version: v3•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

The mechanism of action is defined as the biochemical or physical process that occurs at the ___ to produce the pharmacological effect.

Back (Answer)

site of action.

#2
Front (Question)

For drug administration, the parenteral route is defined as…

Back (Answer)

Outside the intestine (i.e., IV, IM, SQ, etc.).

#3
Front (Question)

Drug action is ___ mediated at the cellular membrane.

Back (Answer)

receptor.

#4
Front (Question)

For drug administration, GI absorption can include…

Back (Answer)

Rectal/suppository.

#5
Front (Question)

The rate of absorbance is classified by which two biochemical methods?

Back (Answer)

Passive diffusion and dietary transport mechanism.

#6
Front (Question)

Which GI changes can affect drug absorption?

Back (Answer)

GI motility, pH, inflammation, food, and other drugs.

#7
Front (Question)

Define first pass metabolism.

Back (Answer)

a drug gets metabolized at a specific location in the body that results in a reduced concentration of the active drug upon reaching its site of action or the systemic circulation.

#8
Front (Question)

Which drug type correlates with therapeutic and toxic physiological effects? (Bound or Free)

Back (Answer)

Free drug.

#9
Front (Question)

Which two factors effect the amount of free drug available?

Back (Answer)

(1) Serum protein level; (2) Competitive binding for the receptor on the transport protein.

#10
Front (Question)

What is the major site of metabolic clearance and biotransformation?

Back (Answer)

Liver.

#11
Front (Question)

Unmetabolized drugs are termed the ___ compound; metabolized products are termed ___.

Back (Answer)

parent; metabolites.

#12
Front (Question)

Define xenobiotic.

Back (Answer)

Exogenous substances (drugs) that are capable of entering the metabolic pathway.

#13
Front (Question)

Describe Phase I enzyme reactions.

Back (Answer)

Chemical structure modification produces reactive intermediates.

#14
Front (Question)

What is the enzyme responsible for Phase I Enzyme reactions?

Back (Answer)

Cytochrome P450.

#15
Front (Question)

Describe Phase II Enzyme reactions.

Back (Answer)

The drug becomes water soluble because of the conjugation of the functional group.

#16
Front (Question)

How does the depletion of conjugate groups effect Phase I & II enzyme reactions?

Back (Answer)

Can create a backup of Phase I reactive intermediates which may become toxic.

#17
Front (Question)

How are free form drugs and metabolites eliminated by renal clearance?

Back (Answer)

Glomerular filtration - renal secretion through the tubules.

#18
Front (Question)

The rate of drug clearance correlates with ___ clearance.

Back (Answer)

creatinine.

#19
Front (Question)

How will a decreased GFR effect serum half life and concentration?

Back (Answer)

It will cause it to increase.

#20
Front (Question)

An IV bolus of a drug is what type of elimination?

Back (Answer)

First-order.

#21
Front (Question)

Define half life.

Back (Answer)

Time required for the concentration to be decreased by one half.

#22
Front (Question)

Define the drug distribution rate.

Back (Answer)

How long it takes the drug to distribute throughout the body.

#23
Front (Question)

Define minimum effective concentration (MEC).

Back (Answer)

Lowest concentration of the drug in the blood that will produce the desired result.

#24
Front (Question)

Define minimum toxic concentration (MTC).

Back (Answer)

The lowest concentration of the drug in the body that will produce an adverse response.