Parmacology Flashcards

0
Q

Dipyrone

A

May be similar w/ Tylenol on mechanism

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1
Q

Paracetamol

A

acetaminophen

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2
Q

Nefopam

A
  1. Not anti-inflammatory

2. Not antipyretic

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3
Q

Tapentadol

A
  1. Nucynta
  2. Mu + norepinephrine reuptake inhibitor
  3. 100mg = 15 mg oxycodone
  4. Q4-6 hrs
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4
Q

Peripherally acting mu-opioid antagonists

A
  1. Methylnaltrexone

2. Albino pan: increase MI in one study

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5
Q

Fentanyl patch

A
  1. transdermal: equivalent to parenteral fentanyl

2. upon patch removal—>serum contration reduce by 50% per 17 hrs.

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6
Q

Incomplete cross tolerance

A

reduction in anticipated dose following opioid rotation and conversion. Typically this involves an initial dose 25-50% lower than calculated.

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7
Q

histamine release

A

Morphine, meperidine and codeine are three opioids whose administration can result in histamine release

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8
Q

Tertiary amine agents vs secondary amines

A

3rd: amitriptyline, imipramine—>=inhibiting norepinephrine and serotonin
2ed: nortriptyline, desiprine—> favor epi

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9
Q

Celecoxib

A
  1. clinically most cox-2 selective NSAID

2. increase adverse cardiac events: MI, stroke

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10
Q

Naproxen

A
  1. opposite celecoxib
  2. likely most cox-1 selective
  3. lowest cardiovascular risk of available NSAIDS
  4. Increase peptic ulceration & GIB–>Px: PPI, H2-blocker
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11
Q

acetaminophen

A
  1. mechanism poorly defined
  2. COX-2 inhibitor in vitro
  3. COX-3 (splice variant of COX-1) inhibitor in CNS
  4. NNT: 4-5
  5. IV: start 5min, peak 1hrs, last 4-5 hrs.
  6. NAPQI–>hepatic toxicity
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12
Q

clonidine vs dexmedetomidine

A
  1. dex: 7 fold greater affinity

2. clonidine: more hemodynamic instability

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13
Q

NMDA antagonists

A
  1. ketamine: strong

2. methedone: weak

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14
Q

sub-anesthetic dose of ketamine

A
  1. perioperative analgesia
  2. reducing opioid
  3. rescue analgesics
    $$: hallucination, dizziness, sedation, out-of-body sensation, nightmare
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15
Q

Naprosyn = naproxen

A
  1. noselective NSAID

2. relatively risk-neural cardiovascular profile