Part 1 Flashcards

1
Q

Drugs that may require reduced dosing in elderly and side effects

A
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2
Q

Drugs with potential teratogenic effects

A
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3
Q

Drugs to be aware in common diagnoses

A
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4
Q

Common drug interactions

A
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5
Q

Drugs that may cause constipation

A
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6
Q

Drugs that may cause constipation

A
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7
Q

Drugs that may cause confusion

A
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8
Q

Drugs that may cause diarrhea

A
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9
Q

Drugs that may cause dyspepsia

A
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10
Q

Drugs that may cause falls/dizziness

A
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11
Q

Drugs that may cause hearing loss

A
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12
Q

Tremor causing drugs

A
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13
Q

Red flag signs in children (infection)

A

Several red (high risk) signs and symptoms:
tachypnoea (RR >60/min)
temperature ≥ 38°C
pale, mottled skin
lethargy

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14
Q

What do ADR frequency equate to in percentage

A
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15
Q

Common side effects of Loop diuretics (e.g. furosemide)

A

dehydration, renal impairment, hypokalaemia.

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16
Q

Common side effects of Non-steroidal anti-inflammatory drugs (e.g. ibuprofen)

A

gastrotoxicity, renal impairment, hypertension.

17
Q

Common side effects of Opioid analgesics (e.g. morphine)

A

constipation, confusion, drowsiness, urinary retention.

18
Q

Examples of drugs in which plasma level or biomarker monitoring is required

A

digoxin, gentamicin, vancomycin, antipsychotics, lithium and phenytoin

19
Q

Gentamycin monitoring

A
  • There are no nationally-accepted guidelines for monitoring once-daily dose regimens.
  • Although there are still some advocates for monitoring peak and trough levels with once-daily dosing, that approach is much more time-consuming and more difficult to interpret.
  • For most patients, a nomogram is the method of choice in order to confirm or modify dosing intervals. For a daily dose of 7 mg/kg/day, the Hartford nomogram can be used.
  • Gentamicin levels should be taken between 6–14 (16-18 in our guideline) hours after the start of the infusion (the Urban-Craig nomogram is an alternative for a daily dose of 5mg/kg/day)
  • Normal/stable renal function: re-check gentamicin levels every 2-3 days
  • Impaired renal function: gentamicin level required before each dose
  • If the dose is adjusted, repeat levels should be taken 18 - 22 hours after the dose change
  • U&Es should be checked every 2-3 days (daily if CrCl < 40ml/min)
  • All patients prescribed more than one dose of gentamicin should have a fluid balance chart completed and urine output should be closely monitored
20
Q

Once daily vs multiple daily gentamycin safety and effectiveness

A

Once-daily dosing of gentamicin has been shown to be at least as effective as and not more toxic than a multiple-daily dosing regimen

21
Q

Contra-indication to gentamycin

A

Myasthenia gravis

22
Q

Who is once daily dosing of gent not appropriate?

A

Once-daily dosing not appropriate in:
- Endocarditis or Pregnancy - use multiple-daily (conventional) gentamicin dosing regimens
- Ascites, Burns, Cystic Fibrosis - refer to Microbiologist

23
Q

Interpreting once daily dosing gent and when should it be measured

A

Post-dose Level

  • <1 mg/L
    Continue gentamicin at current dose
    1-2mg/L
    Wait until the level is <1mg/L and then HALVE current dose, give this dose, then re-check levels 18-22 hours post-dose
    ->2mg/L
    STOP gentamicin and contact Consultant Microbiologist or Pharmacist for advice

Normal/stable renal function: re-check gentamicin levels every 2-3 daysImpaired renal function: gentamicin level required before each dose

24
Q

Gentamycin treatment duration

A

DO NOT continue treatment for longer than 5 days without discussion with Microbiology or referral to the Microbiology ward round on Tuesdays and Thursdays

25
Q

Lithium monitoring

A

Samples taken at least 6 hours post-dose. Target concentration is 0.4–1.0 mmol/L.

26
Q

Vancomycin target levels and when test should be taken

A

A pre-dose (trough) concentration should be taken after 3–4 doses. Target concentration 10–15 mg/L (15–20 mg/L for severe infections or less sensitive organisms)

27
Q

Digoxin target levels and when test should be taken

A

Samples should be taken at least 6 hours post-dose. Efficacy is best determined with a clinical endpoint (e.g. heart rate). The risk of toxicity increases progressively at concentrations >1.5 microgram/L (1.92 nmol/L), and becomes likely at concentrations >3.0 microgram/L (3.84 nmol/L).