Class 3 - Principles of Pharmacology Flashcards

1
Q

pharmacokinetics

A

the process of a drug movement through the body. all drugs go through the 4 stages

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2
Q

pharmacodynamics

A

the study of the effect of a drug on cells, and the drugs mechanism of action

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3
Q

what are the 4 stages of pharmacokinetics

A

absorption, distribution, metabolism, excretion

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4
Q

absorption

A

process of moving a substance from its site of administration, across the body membranes to the bloodstream.
depends on size, lipid solubility, degree of ionization, and interaction with food and other drugs
the more rapid the absorption, the faster the onset of drug action
acids will absorb in acids, bases will absorb in bases

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5
Q

first past effect

A

drug goes to liver after taking orally

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6
Q

bioavailability

A

the amount of drug that reaches the target.

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7
Q

what are factors that could affect drug absorption?

A

taking other drugs, what’s in your gut, certain acidic and non-acidic environments

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8
Q

distribution

A

describes how drugs are transported through the body to receptor sites. how a drug becomes available to body fluids and body tissues.

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9
Q

what influences distribution?

A

blood flow, the drugs solubility, the drugs affinity to the tissue, protein binding effect, dehydration, blood viscosity, placental barriers

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10
Q

what is the protein binding effect?

A

some drugs bind to a protein so they need to be taken with a meal

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11
Q

metabolism

A

also known as biotransformation. process of chemically converting a drug to a form that is usually removed from the body more easily. makes it more likely to be excreted.

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12
Q

what is the primary site of metabolism?

A

the liver, kidneys are secondary

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13
Q

what factors might affect metabolism?

A

hepatitis, diseases that attack or damage the liver, cirrhosis (liver scaring)

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14
Q

excretion

A

remove drug metabolites from the body and only sometimes the actual drug itself

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15
Q

where are drugs excreted?

A

usually the kidneys but may also be excreted by the lungs or glands, or into bile (sweat, feces, urine, breast milk)

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16
Q

half life

A

length of time for 50% of a drug to be absorbed. by knowing the half life we can determine dosing schedules

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17
Q

what can affect the half life?

A

metabolism and elimination.

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18
Q

therapeutic range

A

drug concentration between the minimal effective concentration and toxic concentration

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19
Q

agonist

A

drugs that produces a response the same as the endogenous substances

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20
Q

antagonist

A

drug that prevents a response from endogenous chemical

21
Q

idiosyncratic effect

A

individualized, unpredictable and unexplained drug reactions

22
Q

adverse effect

A

undesirable and potentially harmful action caused by the administration of a medication

23
Q

partial agonist

A

medication that produces a weaker, or less effective response than an agonist

24
Q

polypharmacy

A

the taking of multiple drugs

25
Q

synergistic effect

A

the combined effect of two different drugs is greater than the sum of the effect of each drug taken alone

26
Q

tolerance

A

adapting to a drug over a period of time and subsequently requiring higher doses to achieve the same effect

27
Q

physical dependance

A

experiencing unpleasant withdrawal symptoms when a substance is discontinued

28
Q

allergic reaction

A

acquired, immune system response to a foreign substance

29
Q

anaphylaxis

A

extreme hypersensitivity to an antigen and may lead to life threatening shock if untreated

30
Q

dissolution

A

the first phase of drug action for oral medication. the drug goes into solution so that it can cross the biological membrane. when the drug is administered by injection or topically, there is no pharmaceutic phase

31
Q

what are the stages of dissolution?

A

tablets-disintegration-dissolution

32
Q

onset of action

A

the time it takes to reach the minimum effective concentration after drug administration

33
Q

what is peak action

A

when the drug reaches its highest blood or plasma concentration

34
Q

duration of action

A

the length of time the drug has a pharmacologic effect

35
Q

trough

A

lowest level of drug before administering another dose

36
Q

drug receptor theory

A

the activity of many drugs is determined by the availability of the drug to bind to a specific receptor. the better the drug fits at the receptor store, the more biologically active it is. most receptors are found on cell membranes

37
Q

cumulative effect

A

when the effects of a drug increase due to retention of the drug in the body

38
Q

additive effect

A

two of the same drugs with similar action are taken for a doubled effect

39
Q

side effect

A

predictable, less serious drug effect

40
Q

enteric-coated

A

a tablet is coated with a substance that prevents the medication from being released until it reaches the small intestine, where it can then be absorbed

41
Q

parenteral administration

A

injection or infusion. common types of injection are intravenous (into a vein), subcutaneous (under the skin), and intramuscular. the most common infusion is intravenous

42
Q

what is cirrhosis

A

liver scarring

43
Q

therapeutic response

A

onset of action, peak action, duration of action, therapeutic range

44
Q

what is another name for metabolism

A

biotransformation

45
Q

what determines the route of administration?

A

the form the medication is in

46
Q

topical

A

hormones that influence the activities of a certain gland

47
Q

nephrotoxicity

A

toxicity of kidneys

48
Q

IM

A

intramuscular