lecture 1 - intro to pharm Flashcards

pharmacokinetics, pharmacodynamics, bioequivalence, OTC, Prescription drugs, therapeutic index, common routes, drug delivery

1
Q

areas of study within pharmacology

What is the study of therapuetic effects of drugs called?

A

pharmacotherapeutics

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2
Q

areas of study within pharmacology

what is the study of harmful effects of drugs called?

A

toxicology

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3
Q

areas of study within pharmacology

what is the study of how the body absorbs, distributes, and elimates the drugs called?

A

pharmacokinetics

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4
Q

areas of study within pharmacology

analysis of what the drug does to the body, including the mechanism by which the drug exerts its effect called?

A

pharmacodynamics

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5
Q

drug nomeclature

referes to the specific compounds structure.

Usually fairly long and cumbersome

A

chemical name (example: benzodiazepin)

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6
Q

drug nomeclature

nonproprietary name

A

generic name (example: diazepam)

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7
Q

drug nomenclature

brand name assigned by the pharmaceutical company

A

trad name (example:valilum)

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8
Q

same type and amount of active ingredients, same administration route, same pharmacokinetic profile, same therapeutic effects

A

generic vs name brand drugs

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9
Q

Bioequivalent does not guarantee what 2 things?

A
  1. that patients will not experience different effect from brand name drug
  2. lower overall health care expenses (if adverse effects persent)
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10
Q
A
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11
Q

non-prescription vs perscription

what are the 5 benefits of OTC medications?

A
  1. can be purchased directly by consumer
  2. improved access
  3. relatively nimor problems
  4. lower risk of toxicity
  5. may have lower therapeutic effect and cause a delay in a more appropriate prescription medication
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12
Q

drug safety

waht is the therapeutic index (TI) equation?

A

median toxic dose / median effective does = TI

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13
Q

drug safety

is a higher or lower TI considered safer? why?

A

A higher TI is safer.
This is because it takes more for the medication to be considered toxic

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14
Q

pharmacokinetics - administration

waht are the two primary routes for pharmacokinetic administration?

A
  1. enteral (alimentary canal/the whole passage along which food passes through body)
  2. parenteral (nonalimentary routes)
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15
Q

administration - enteral

what are the 3 advantages of oral administrtion?

A

easy
safe
convenient

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16
Q

administration - enteral

what are the 2 disadvantages of oral administration?

A

limited/erratic absorption
change offirst pass inactivation in liver

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17
Q

administration - enteral

what are the 2 advantages of sublingual/buccal administration?

A

rapid onset
not subject to first pass inactivation

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18
Q

administration - enteral

What is the distadvantage of sublinual/buccal administration?

A

must be easily absorbed from oral mucosa

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19
Q

administration - enteral

what are the 2 advantages to rectal administration?

A

alternative to local rout
local effect on rectal tissues

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20
Q

administration - enteral

What are the 2 disadvantages of rectal administation?

A
  • poor/incomplete absorption
  • chance of rectal irritation
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21
Q

administration - parenteral

what are the 3 advantages of inhalation administration?

A
  • rapid onset
  • direction application to respiratory disorders
  • large surface area for systemic absorption
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22
Q

administration - parenteral

what are the 2 disadvantages of inhalation administration?

A
  • chance of tissue irritation
  • lower compliance
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23
Q

administration - parenteral

what are the 2 advantages of injection administration?

A
  • direct administration to target tissue
  • rapid onset
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24
Q

administration - parenteral

what are the 2 disadvantages of injection administration?

A
  • higer risk of infection
  • injection done incorrectly (for example: nerve root irritation)
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25
Q

administration - parenteral - injection

What are the 5 types of parenteral inejctions?

A
  • intramuscular (IM)
  • intrathecal
  • IV
  • intra-arterial
  • subcutaneous
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26
Q

administration - parenteral - injection

what type of injection can treat the problem located directy in the inected muscle? can provide realtively steady, prolonged release of drug into systemic circuation?

A

intramuscular (IM)

27
Q

administration - parenteral - injection

What is one downside to IM injection?

A
  • one down side is significant local pain and prolonged soreness, limited use for repeated administration
28
Q

administration - parenteral - injection

What type of injection delivers medication within a sheath? gain better access to spinal cord by injecting into subarachnoid space?

A

intrathecal

29
Q

administration - parenteral - injection

what type of injection allows drug to bypass the BBB to reach CNS?

A

intrathecal

30
Q

administration - parenteral - injection

what type of injection has increased bioavailabililty? accurate/known quantity into blood stream over short period of time? is helpful whe nemds needed in emergency situations to exerct immediate effect?

31
Q

administration - parenteral - injection

what injection type has peak levels of the drug achieved almost instantaneously in peripheral circulation?

32
Q

administration - parenteral - injection

what type of injeciton has increased bioavailability? is difficult, dangerous and often used in chemotherapy?

A

intra-arterial

33
Q

administration - parenteral - injection

Intra arterial injection may be used to administer what?

A

radiopaque dye for diagnostic procedures

34
Q

administration - parenteral - injection

what type of injection can permit slower/prolonged release of medication into systemic circulation (like insulin)

A

subcutaneous

35
Q

bioavailability

what is bioavailabilty of a drug?

A

percentage of the drug administered taht reached the bloodstream

36
Q

bioavailability

if 100mg of medication is taken orally, what is its bioavailability?

A

50% (50 mg eventually make it into the bloodstream)

37
Q

bioavailability

if 100mg of medicatioin is inected via IV, what is its bioavailability?

38
Q

pharmacokinetics - absorption

T/F drugs MUST move across cell membranes and tisue barriers?

39
Q

pharmacokinetics - absoprtion

what are cell membranes rimarily composed of?

A

lipids and proteins

40
Q

pharmacokinetics - absorption

how do drugs usually pass through the memebrane?

A

by dissolving in the lipid bilayer

41
Q

pharmacokinetics-absorption

substances such as _________ pass through small pores

A

water

depends on size, shape, electrical charge of the molecule

42
Q

pharmacokinetics - distribution

what are the 4 factors that affect distribution?

A
  1. tissue permeability
  2. blood flow (disease that would cause decrease in blood flow)
  3. binding to plasma proteins
  4. binding to subcellular components
43
Q

pharmacokinetics - distribution

where is the primary site for drug storage?

A

adipose tissue

stays for a long time

44
Q

pharmacokinetics - distribution

acts as storage for several toxic agents (heavy metals and lead)

45
Q

pharmacokinetics - distribution

often stored within certain organs namely _______ and ________

A

liver and kidneys

46
Q

T/F liver and kidneys are often subjected to local damage when these organs must deal with higher concentration of therapeutic agents?

47
Q

how is the drug prevented from reaching target site?

A

reservoir “soaks up” the drug and prevents it

48
Q

what can happen to the storage sites of drugs in the body?

A

storage sites can leak the drug for redistribuiton for prolonged effect

49
Q

what are the 3 newer delivery techniques for drugs?

A
  1. controlled release
  2. implanted
  3. trageted delivery
50
Q

what delivery technique permits slower/prolonged absorption, decreases number of doses needed each day and preverts large fluctuations in drug concentratioin?

A

controlled relase (example: anti parkinsons drugs)

51
Q

what type of drug delivery technique releases a small, measured dose of drug on pre-programmed schedule and can be manually controlled for greater patient control of dosage?

52
Q

what type of delvery technique focuses the drug effects on specific tissues and reduces side effects?

A

targeted delivery

53
Q

pharmacokinetics - elimination

what are the 4 biotransformation reactions?

A
  1. oxidation
  2. reduction
  3. hydrolysis
  4. conjugation
54
Q

pharmacokinetics - elimination

oxygen is added or hydrogen is removed?

A

oxidation reaction for elimination

55
Q

pharmacokinetics - elimination

oxygen is removed or hydrogen is added?

A

reduction reaction for elimination

56
Q

pharmacokinetics - elimination

broken into separate parts?

A

hydrolysis reaction for elimination

57
Q

pharmacokinetics - elimination

coupled to an endogenous substance

A

conjugation reaction for elimination

58
Q

pharmacokinetics - elimination

what is the primary location for drug metabolism?

59
Q

pharmacokinetics - elimination

Where is the primary sites for drug excretion?

A

the kidneys

60
Q

What is clearance refer to with drug concentration?

A

refers to an organ ortissue’s ability to eliminate the drug

61
Q

what is a half-life?

A

amount of time required for 50% of the drug remaining in the body to be eliminated

disease states can affect clearance and will alter drugs half life

62
Q

drugs are generally _____ metabolized as quickly in the elderly

63
Q

diet is shown to affect what 3 things?

A
  1. absorption
  2. metabolism
  3. response to drugs
64
Q

variation in drug response and metabolism

what 13 things affect drug response?

A
  1. genetics
  2. disease
  3. drug interaction (2 or more drugs)
  4. age
  5. diet
  6. sex
  7. environment
  8. occupation
  9. cigarette smoking
  10. alcohol consumption
  11. obesity
  12. spinal cord injries
  13. extensive burn injuries