Facts Flashcards

1
Q

3 most important properties of drugs

A

effectiveness - has to do what it is supposed to do
safety - there is no completely safe drug
selectivity - one that elicits only desired effects - there is no such thing (all have side effects)

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2
Q

other desired properties

A

reversibility
predictability
ease of administration
freedom from drug interactions
low cost
chemical stability
possession of a simple generic name

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3
Q

reversibility

A

drug actions to subside within an appropriate time (aside from things like antibiotics)

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4
Q

predictability

A

knowing how someone will respond - not guaranteed because everyone is different

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5
Q

ease of administration

A

has two benefits
1 it can enhance patient adherence
2 it can decrease risk. patient more likely to stick to dosing schedule (1 dose per day rather than multiple)

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6
Q

freedom from drug interactions

A

not have bad interactions when taken with other drugs

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7
Q

low cost

A

drugs can be very expensive

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8
Q

chemical stability

A

an ideal drug would retain its activity indefinitely instead of expiring after time

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9
Q

possession of a simple generic name

A

generic names are complex. an ideal drug would have one that is easy to remember

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10
Q

factors that determine the intensity of a drug response

A

administration - dosage, route, timing, adherence, errors
pharmacokinetics - absorption, distribution, metabolism, excretion
pharmacodynamics - drug-receptor interaction, patient’s functional state, placebo effects

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11
Q

5 rights

A

right..
1 drug
2 patient
3 dose
4 route
5 time

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12
Q

drug absorption affecting factors

A

rate of dissolution
absorbing surface
blood flow - high blood flow = high absorption
lipid solubility of drug - high solubility = faster absorption
pH partitioning - acidic drugs - alkaline side of membrane, basic drugs - acidic side of membrane

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13
Q

parenteral meds benefits and problems

A

benefits:
no barriers
rapid onset
can give large amounts of fluids
circulated quickly

problems:
cost, convenience
not reversible
infection, embolism
must be water soluble to be injected

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14
Q

intramuscular (IM) absorption rate

A

10-30 minutes

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15
Q

subcutaneous (SQ) absorption rate

A

blood flow not as good as IM so may be slower

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16
Q

enteral (by mouth via GI) barriers to absorption

A

1 epithelial cells of GI tract lining (biggest barrier)
2 endothelial cells of capillary wall

17
Q

factors affecting enteral (by mouth) absorption

A

solubility
GI pH
gastric emptying
stomach contents
other drugs
drug coating

18
Q

disadvantages of enteral (by mouth)

A

variable absorption
inactivation by food, other drugs, gastric acidity, liver (first pass)
patient must be awake, alert
GI upset

19
Q

other routes of administration

A

topical - skin, eyes, ears, nose, mouth, rectum, vagina
inhaled
rectal suppositories
vaginal suppositories
direct injection - joints, heart, CNS

20
Q

distribution of drug affected by

A

1 blood flow
2 ability to exit the vascular system
3 ability to enter cells

21
Q

drugs that are/have _______ can cross the blood brain barrier

A

lipid soluble
have a transport system

22
Q

an important consequence of drug-protein binding

A

restriction of drug distribution

albumin (most important binding protein) is too large to get through capillary wall, so it stays in the blood stream
drugs that bind albumin cannot leave blood stream either until bond is broken

23
Q

most drug metabolism takes place in

A

the liver

24
Q

results of drug metabolism

A

accelerated renal excretion of drugs
drug inactivation
increased therapeutic action
activation of prodrugs - inactive as administered and is converted into active form via metabolism
increased toxicity
decreased toxicity

25
Q

factors that affect metabolism rate

A

age - infants and elderly are slower
genetic polymorphism - varies by race, geographic location

26
Q

drugs can exit the body in

A

urine, bile, sweat, saliva, breast milk, and expired air

27
Q

the most important organ for excretion is

A

the kidney

28
Q

steps in drug elimination

A

1 filtration
2 reabsorption (lipid soluble drugs undergo passive reabsorption from tubule back into blood)
3 secretion (pumps move drugs from blood into urine)

29
Q

factors affecting secretion

A

pH (manipulating pH can hasten the drugs elimination - for poisoning and toxic doses of meds)
competition for active tubular transport (can only transport so much at a time - competition might prolong the effects of drugs)
age (newborn’s have limited capacity to excrete drugs because of undeveloped kidneys - old age causes renal function decline which decreases excretion of drugs)

30
Q

plasma drug level used to predict therapeutic or toxic affects because

A

it is hard to measure drug concentration at sites of action. easier to calculate therapeutic or toxic affects based on blood plasma

31
Q

drug-receptor interactions

A

1 drugs most often act as the body’s own receptor sites for hormones, neurotransmitters, etc.
2 drug can only mimic or block actions of substance that normally interact with that receptor
3 drugs can not give cells new function
4 drug interaction with a receptor is like a lock and key (very specific)

32
Q

variability in drug responses

A

amount of drug required for therapeutic response can vary
not always easy to predict
ED50 - standard dose, fine tuned for each patient