Clinical Perals Flashcards

(39 cards)

1
Q

the prototype of pure mu agonist

A

morphine

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2
Q

pruritis is common

A

morphine

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3
Q

5-7x more potent than morphine

A

hydromorphone

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4
Q

less pruritis, sedation and nausea

A

hydromorphone

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5
Q

better analgesic option than morphine in patients with renal impairment

A

hydromorphone

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6
Q

1.5-2x more potent than morphine

A

oxycodone

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7
Q

black box warning for concomitant use with 3A4 inhibitors of discontinuation of 3A4 inducers could increase levels

A

oxycodone

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8
Q

don’t use IM formulation

A

morphine, hydromorphone

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9
Q

oxycodone ER products: abuse-deterrent formulation

A

Xtampza

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10
Q

indication for xtampza

counseling point

A

the management of pain severe enough to require daily, around-the-clock, long-term opioid treatment and for which alternative treatment options are inadequate. Do not use prn

must be taken with food

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11
Q

take on an empty stomach; bioavailability increases with food administer 1 hour before or 2 hours after eating

A

oxymorphone

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12
Q

black box: do not use with alcohol

A

oxymorphone

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13
Q

doses greater than 5mg q12h are for opioid-tolerant patients only

A

oxymorphone

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14
Q

dual action opioid: centrally acting mu agonist + inhibits NE uptake

A

tapentadol

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15
Q

FDA indicated for the treatment of DPN and treatment of moderate to severe pain

A

tapentadol

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16
Q

do not use concurrently with MOA inhibitors or within 14 days

17
Q

doses greater than 50mg po 12h are for opioid-tolerant patients only

18
Q

centrally acting weak mu partial agonist + inhibits NE and 5HT

19
Q

naloxone only partially effective

20
Q

seizure risk for at-risk pts, reports of increased risk of hypoglycemia and hyponatremia

21
Q

tramadol CIs

A

children <12
children <18 post op from tonsillectomy or adenoidectomy
do not use with MOAs or within 14 days
12-18 obese
strong warning: breast feeding mothers

22
Q

analgesic activity of tramadol comes from

23
Q

analgesic activity of tapentadol comes from

24
Q

FDA approvals: OUD & moderate to severe pain

A

buprenorphine

25
starting this drug when a pt is opioid-tolerant increases risk of possible withdrawal reactions
buprenorphine
26
taper in a physically dependent patient
butrans
27
mu agonist, SNRI, NMDA receptor antagonist
methadone
28
QTc prolongation: ECG recommendations
methadone
29
watch out for amiodarone anti-infectives and antidepressant
methadone
30
elimination half life of methadone
15-130 hours mean 15-40 4-10 days steady stte
31
possible methadone candidates
pts with true morphine allergy pts with significant renal impairment pts with significant neuropathic pain pts who have failed other opioids; ADRs to other opioids cost issues with other opioids long-acting opioid requirement
32
patients who may not be candidates for methadone therapy
poor prognosis, end of life polypharmacy, risk of numerous drug interactions risk of QT prolongation, hx of arrhythmias/syncope hx of poor adherence, lives alone hx of substance abuse
33
80-110 times more potent than morphine
fentanyl
34
BBW: 25 mcg patch use in tolerant patients only do NOT use in acute pain concomitant use of potent cyp3a4 inhibitors can increase fentanyl levels
fentanyl
35
minimal conc of fentanyl maximal conc ave steady state
12 36 3-6 days
36
active metabolite can accumulate in 2 days leading to significant neurotoxic ADRs which are not reversible by naloxone
meperidine
37
do not use greater than 48 hours avoid in patient with renal dysfunction do not use for chronic pain management
meperidine
38
metabolized in liver prodrug: requires metabolism via CYP2D6 to morphine
codeine
39
codeine CI
should not be used to treat cough in children younger than 12 years