Clinical Perals Flashcards
(39 cards)
the prototype of pure mu agonist
morphine
pruritis is common
morphine
5-7x more potent than morphine
hydromorphone
less pruritis, sedation and nausea
hydromorphone
better analgesic option than morphine in patients with renal impairment
hydromorphone
1.5-2x more potent than morphine
oxycodone
black box warning for concomitant use with 3A4 inhibitors of discontinuation of 3A4 inducers could increase levels
oxycodone
don’t use IM formulation
morphine, hydromorphone
oxycodone ER products: abuse-deterrent formulation
Xtampza
indication for xtampza
counseling point
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
take on an empty stomach; bioavailability increases with food administer 1 hour before or 2 hours after eating
oxymorphone
black box: do not use with alcohol
oxymorphone
doses greater than 5mg q12h are for opioid-tolerant patients only
oxymorphone
dual action opioid: centrally acting mu agonist + inhibits NE uptake
tapentadol
FDA indicated for the treatment of DPN and treatment of moderate to severe pain
tapentadol
do not use concurrently with MOA inhibitors or within 14 days
tapentadol
doses greater than 50mg po 12h are for opioid-tolerant patients only
tapentadol
centrally acting weak mu partial agonist + inhibits NE and 5HT
tramadol
naloxone only partially effective
tramadol
seizure risk for at-risk pts, reports of increased risk of hypoglycemia and hyponatremia
tramadol
tramadol CIs
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
analgesic activity of tramadol comes from
metabolite
analgesic activity of tapentadol comes from
parent
FDA approvals: OUD & moderate to severe pain
buprenorphine