drugs week 1 Flashcards

(45 cards)

1
Q

define anatomy

A

the study of structure

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2
Q

define physiology

A

the study of function

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3
Q

define pathophysiology

A

the study of disease processes

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4
Q

Australian drug authority ?

A

TGA - therapeutic drugs administration

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5
Q

define adverse drug reaction

A

undesirable response to drug

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6
Q

side effect

A

desirable or undesirable response to drug

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7
Q

indication?

A

illness or disorder for which the drug is used

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8
Q

approved name of drug

A

generic

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9
Q

drug-company name of drug

A

brand/trade name

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10
Q

drug classification - what is S2

A

pharmacy medicine

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11
Q

drug classification - what is S3

A

pharmacist only

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12
Q

drug classification - what is S4

A

prescription only

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13
Q

drug classification - what is S8

A

controlled drugs

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14
Q

drug classification - what is S9

A

prohibited drugs

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15
Q

define pharmacodynamics

A

how the drug affects the body

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16
Q

define pharmacokinetics

A

how the body affects the drug

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17
Q

define agonist

A

binds with receptor to cause an effect in the cell

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18
Q

define antagonist

A

binds with receptor to block any effect in the cell(occupies but does not activate the drug receptor)

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19
Q

receptor upregulation is…

A

chronic absence of agonist

20
Q

receptor down regulation is…

A

chronic excess of agonist

21
Q

ADME

A

absorption, distribution, metabolism, excretion

22
Q

blood vessels from the intestine transport substances first via the BLANK to the BLANK

A

hepatic portal vein to the liver

23
Q

the amount of drug metabolised by the liver is called…

A

hepatic first pass metabolism

24
Q

which routes avoid hepatic first pass

A

buccal, sublingal, some rectal (50%)

25
which is the fastest of the parenteral routes
IV
26
which is faster subcut or IM
IM - better blood supply
27
what protein can bind to drugs in the blood and slow down their distribution ?
albumin
28
define enterohepatic circulation
drugs are cycled from liver to bile(gallbladder) to small intestine via hepatic portal vein back to liver
29
main site of metabolism
liver
30
name a liver enzyme
CYP (cytochrome P450)
31
what are prodrugs
drugs that are metabolised into their more active form
32
after metabolism are drugs more or less active
less
33
site of most excretion
kidneys(but also the liver through bile, faeces)
34
site of filtration in the nephron
glomerulus
35
define therapeutic range
drug concentration in blood which produces clinical benefit
36
define half life
time for the amount of drug in plasma to half - longer half life, longer in the effective range
37
define regular dosing
when drug is given repetitively in a fixed dose at fixed intervals it accumulates in body, reaching a plateau in the therapeutic window
38
define receptor
Protein structure on or within a cell or membrane that is capable of binding to a specific substance (such as a transmitter, hormone or drug), initiating chemical signalling and causing altered function in the cell
39
define selectivity
the narrowness of a drug's range of actions - which depends what particular receptors it binds to
40
define specificity
refers to the relationship between the chemical structure of a drug and its pharmacological actions - this affects what organ/tissues it will act upon
41
name any of the sources of drugs
micro-organisms(fungi, bacteria, yeasts etc),minerals, plants ,animals, synthesised in laboratory
42
what is a proscribed drug
a prohibited drug
43
what is bioavailability
the proportion of the dose that reaches the systemic circulation
44
Whats a prototype drug
the most important drug in its class - to which other drugs can be compared ie.insulin is prototype diabetes agent
45
define contra-indications
the medical conditions in which a drug should NOT be prescribed