Pharmacology Flashcards

(36 cards)

1
Q

What is pharmacology

A

the study of drugs - their sources, nature, actions, effects and uses

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2
Q

define a drug

A

any substance causing physiological changes, whether legal/illegal, medicinal/recreational, natural/synthetic

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3
Q

what are the 3 types of drug names

A

Trade (brand), generic, chemical

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4
Q

what are the 4 pharmacokinetic processes

A

Absorption, distribution, metabolism, excretion (ADME)

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5
Q

where does metabolism mostly occur

A

in the liver

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6
Q

how are drugs mostly excreted

A

via the kidneys (urine)

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7
Q

what is the first pass-effect

A

metabolism of oral drugs by the liver before systemic circulation

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8
Q

how does asprin relieve pain

A

by inhibiting COX enzymes

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9
Q

define efficacy

A

the maximum effect a drug can produce

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10
Q

define potency

A

the amount of drug needed to produce a given effect

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11
Q

define selectivity

A

how selectivity a drug targets specific receptors / enzymes

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12
Q

define specificity

A

how exclusively a drug binds to its intended target

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13
Q

what are indications and contraindications

A

indications: conditions the drug is used to treat
contraindications: conditions where the drug should not be used

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14
Q

what are adverse drug reactions (ADR’s)

A

harmful or unintended effects at normal doses

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15
Q

what is bioavailability

A

percentage of a a drug that reaches systemic circulation

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16
Q

define half life

A

time for plasma concentration to reduce by 50%

17
Q

how long to reach steady-state concentration

A

about 4-5 half lives

18
Q

what affects absorption

A

absorbing surface, chemical structure, membrane crossing

19
Q

what is distribution

A

movement of drug to tissues via bloodstream

20
Q

what affects drug activity in plasma

A

binding to plasma proteins (only free drug is active)

21
Q

what are the 4 main drug targets

A

receptors, enzymes, carrier molecules, Ion channels

22
Q

what do agonists and antagonists do

A

agonists: activate receptors
antagonists: block receptors

23
Q

what is competitive enzyme inhibition

A

drug competes for the active site, reversible

24
Q

what is non-competitive enzyme inhibition

A

drug binds elsewhere, alters enzyme shape, not reversible by adding substrate

25
what routes are enteral and what is the advantages / disadvantages of these routes
oral, sublingual, rectal +: easy, safe, non-invasive, self administered -: slower onset, first pass metabolism, affected by GI factors
26
why use IV to administer drugs
immediate effect, emergency use
27
why use IM
slower than IV, useful for sustained release
28
why are sublingual routes used
rapid absorption, bypasses the liver
29
why use rectal
when oral route not possibel, partial liver bypass
30
why use topical
local effect, minimal systemic absorption
31
why use inhaler
direct lung delivery, fast local action
32
why use vaginal route
local or systemic delivery, GI bypass
33
what is sustained release
gradual drug release, longer effect, fewer doses
34
what is enteric coated
protects drug from stomach acid, dissolves in intestine
35
advantages of capsules
easier to swallow, taste masking
36
what affects rate of drug action
route of administration and drug formulation