tricyclics, tamoxifen, heparin, lorazepam, haloperidol, ACEi Flashcards

1
Q

sedative tricyclic examples

A
  • amitriptyline
  • clomipramine
  • dosulepin
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2
Q

less sedative tricyclic examples

A
  • imipramine
  • nortriptyline
  • lofepramine
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3
Q

adverse effects of tricyclics

A

blockade of antimuscarinic receptor:

  • dry mouth
  • constipation
  • urinary retention
  • blurred vision

Blockade of H1 and α1 receptors:

  • sedation
  • hypotension
  • prologation of QT + QRS
  • convulsions, hallucinations, mania
  • breast changes, sexual dysfunction
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4
Q

TCA overdose effects

A

severe hypotension, arrhythmias, convulsions, coma

and respiratory failure

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5
Q

TCA sudden withdrawal sx

A

GI upset, neuro + influenza-like sx and sleep disturbance

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6
Q

TCA should not be given with what drug

A

monoamine oxidase inhibitors

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7
Q

what is venlafaxine

A

SNRI

serotonin and noradrenaline reuptake inhibitor

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8
Q

what is mirtazapine

A

antagonist of inhibitory pre-synaptic α2-adrenoceptors.

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9
Q

how does venlafaxine and mirtazipine work

A

Both drugs increase availability of monoamines for

neurotransmission

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10
Q

important adverse effects of venlafaxine and mirtazipine

A
  • GI upset
  • headache, abnormal dreams, convulsopms
  • Suicidal thoughts and behaviour
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11
Q

when should mirtazapine be taken

A

at night ot minimus its sedative effects

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12
Q

the most common adverse effects of statins

A

headache and GI disturbance

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13
Q

more serious effects of statins

A

myopathy

rhabdomyolysis

rise in ALT

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14
Q

important interactions with statins

A

The metabolism of statins is reduced by cytochrome P450
inhibitors, such as amiodarone, diltiazem, itraconazole, macrolides

amlodipine

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15
Q

when are statins taken

A

evening, as there is some evidence

that they have a greater effect when dietary intake is at its lowest.

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16
Q

what should pts on statins avoid drinking

A

grapefruit juice

17
Q

how should efficacy of statins be monitored

A

checking target cholesterol levels are achieved

18
Q

for safety, what should be measured at baseline and again at 3 and 12 months when on a statin

A

ALT

check TFT before starting

19
Q

methotrexate adverse effects

A
  • mucosal damage
    (e. g. sore mouth, gastrointestinal upset)
  • bone marrow
    suppression (neutropenia and an
    increased risk of infection)
20
Q

long term use of methotrexate can result in what

A

hepatic cirrhosis or pulmonary fibrosis

21
Q

important interaction of methotrexate

A

e toxicity is more likely if it is prescribed with drugs that
inhibit its renal excretion, e.g. NSAIDs, penicillins

Co-prescription
with other folate antagonists, e.g. trimethoprim and phenytoin,
increases the risk of haematological abnormalities

22
Q

prescription of methotrexate

A

once weekly

IV or intrathecal

Folic acid 5 mg can be prescribed to be
taken on the 6 days where methotrexate is not taken

23
Q

monitoring with methotrexate

A

full blood count, liver and renal function before starting
treatment, then 1–2 weekly until treatment is established and
2–3 monthly thereafter

24
Q

what should pts on tamoxifen be warned of

A
  • the risk of endometrial cancer and told to report relevant symptoms promptly
  • symptoms of thromboembolism and advised to report sudden breathlessness and any pain in the calf of one leg.
25
Q

name some LMWH

A

dalteparin and

enoxaparin

26
Q

what is Fondaparinux

A

synthetic compound that is similar to

heparin

27
Q

communication to pt about LMWH and fondaparinux

A
  • avoid activities that may increase their risk of bleeding: contact sports
  • inform healthcare professionals they come into
    contact with that they are taking anticoagulants.
  • train patients how to self-administer SC injections.
  • discuss the risks and benefits of anticoagulation
28
Q

heparin +fondaparinux: what blood tests should be checked

A

FBC + renal profile

In prolonged therapy (>4 days), platelet count should be monitored

29
Q

how should IV lorazepam be given

A

diluted with an equal volume of water for injections or sodium chloride 0.9%.

30
Q

important adverse effects of ACEi

A
  • persistent dry cough
  • hypotension
  • hyperkalaemia
  • renal failure
  • angioedema/ anaphylactoid reaction
31
Q

when is it best to take ACEi

A

best to take the first dose

before bed to reduce symptomatic hypotension.

32
Q

communication about ACEi

A

avoid NSAIDs

33
Q

what should you check before starting ACEi

A

electrolytes and renal function

Repeat these 1–2 weeks into treatment and
after increasing the dose

34
Q

ACEi: Biochemical changes can be tolerated

provided they are within what certain limits

A

creatinine concentration
should not rise by more than 30%, the eGFR should not fall by more
than 25%, and the potassium concentration should not rise above
6.0 mmol/L.