pharmacology Flashcards

1
Q

site of action of osmotic diuretics

A

PT, loop of henle and collecting duct

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2
Q

MOA of osmotic diuretics

A

inhibition of water and Na+ reabsorption

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3
Q

site of action of carbonic anhydrase inhibitors

A

proximal tubules

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4
Q

MOA of carbonic anhydrase inhibitors

A

proximal tubules

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5
Q

MOA of carbonic anhydrase inhibitors

A

inhibition of bicarbonate reabsorption

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6
Q

site of action of loop diuretics

A

thick ascending limb of the loop of henle

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7
Q

MOA of loop diuretic

A

inhibition of Na+, K+ and Cl-

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8
Q

site of action of thiazide diuretics

A

early distal convoluted tubule

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9
Q

MOA of thiazide diuretics

A

inhibition of Na+ Cl- co-transport

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10
Q

site of action of K+ sparing diuretics

A

late DCT and collecting duct

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11
Q

MOA of K+ sparing diuretics

A

inhibition of Na+ reabsorption and K+ secretion

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12
Q

what is the role of the tubules in the nephron

A

reabsorption and secretion of substances and the formation of urine

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13
Q

what is the role of the collecting duct

A

transfers urine to the medullary collecting duct

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14
Q

where does the medullary collecting duct empty into

A

renal papillae in the renal pelvis

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15
Q

what are the components of urinary excretion

A

filtration - reabsorption + secretion

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16
Q

where is blood filtered in the nephron and how is this achieved

A

the glomerulus
passive transport of substances under pressure (due to blood pressure)

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17
Q

what happens in reabsorption in the nephron

A

solutes and water are removed from tubular fluid and transported into the blood

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18
Q

what happens in secretion in the nephron

A

solutes and water are removed from tubular fluid and transported into the blood

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19
Q

how does secretion occur in the nephron

A

active transport

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20
Q

what is natriuresis

A

the process of excretion of sodium in the urine

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21
Q

what 3 substances promote natriuresis

A

VNP and ANP, calcitonin

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22
Q

what substance inhibits natriuresis

A

aldosterone

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23
Q

what is an important drug interaction to remember for loop diuretics

A

greater risk of digoxin toxicity due to hypokalaemia

24
Q

name a type of drug that reduces the efficacy of thiazides

25
Q

name one type of drug that needs to be used with caution with potassium-sparing diuretics

A

ACE inhibitors

26
Q

name an osmotic diuretic

27
Q

how do osmotic diuretics need to be given

A

IV infusion

28
Q

clinical indications for osmotic diuretics

A

prevention of AKI in conditions of reduced renal perfusion
urgent treatment of intracranial and intraocular pressure

29
Q

name a condition that can cause reduced renal perfusion

A

rhabdomyolysis

30
Q

name 3 adverse effects of osmotic diuretics

A

transient expansion of blood volume
hyponatraemia
pulmonary oedema

31
Q

name a carbonic anhydrase inhibitor

A

acetazolamide

32
Q

what is the ending of a CA-I

33
Q

where to carbonic anhydrase inhibitors act

A

proximal convoluted tubule of the nephron

34
Q

what is the MOA of CA-Is

A

reduces HCO3- reabsorption

35
Q

name an adverse effect of CAI’s

A

metabolic acidosis

36
Q

name 2 loop diuretics

A

furosemide and bumetanide

37
Q

name some indications for thiazide diuretics

A

hypertension, heart failure, oedema, nephrotic syndrome

38
Q

name some contraindications for thiazide diuretics

A

hypotension, gout, renal failure, hypokalaemia

39
Q

what are the 2 main types of K+ sparing diuretics and give examples

A

aldosterone antagonists: spironolactone
Na+ channel inhibitors: amiloride

40
Q

what makes adverse drug reactions more likely

A

polypharm, drugs with narrow therapeutic index, multimorbidity, frailty

41
Q

name some drugs with a narrow (<2) therapeutic index

A

warfarin, lithium, digoxin, carbamazepine, levothyroxine

42
Q

what classification is used for ADRs

43
Q

what is a type A adverse drug reaction

A

augmented pharmacological effects - dose dependent and predictable

44
Q

which type of adverse drug reaction has the highest mortality/morbidity

A

type B - bizarre

45
Q

what are type C adverse drug reactions

A

chronic effects which result from prolonged therapy

46
Q

type B ADR from chloramphenicol

A

bone marrow aplasia

47
Q

type B ADR from halothane

A

hepatic necrosis

48
Q

how can we prevent type C ADRs

A

drug therapy monitoring

49
Q

name 3 examples of type C ADRs

A
  • Cushing’s disease from steroid therapy
  • Diabetes from beta blockers
  • hypertension from NSAIDs
50
Q

what are type D ADRs

A

delayed effects, often many years after stopping the drug

51
Q

give an example of a type D ADR

A

secondary malignancy post chemotherapy

52
Q

what are type E ADRs

A

end of treatment effects, can be due to abrupt withdrawal or rebound effects

53
Q

what are type F ADRs

A

failure of therapy

54
Q

what does it mean if a medication has a black triangle

A

still on a list of medicines subject to additional monitoring

55
Q

how often to black triangle medications get reviewed

A

every 2 years

56
Q

what is used to report adverse drug reactions

A

yellow card scheme