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21 Cards in this Set

  • Front
  • Back
Morpine (Admin, distrib, excretion)
Admin - Parenternal 15 times more effective than oral. Has significant first pass metab.
Distrib - 33% protein bound, drug mainly in kidney, liver, lung, and spleen. Not much in CNS
Excretion - Conjugate by liver, glomerular filtration of metabolites and biliary excretion.
Opiod overdose triad
coma, pinpoint pupils, depressed respiration.
Hormonal effects of Morphine
Increased pituitary release of somatotropin, prolactin, and vasopressin.
Decresed pituitary release of lutenizing hormone causing decreased testosterone and sex drive in males.
Opioid withdrawl response
-lacrimation
-rhinorrhea
-perspiration
-goose flesh
-tremors to frank seizures
-anxiety/restless
-increased BP and temp
-vomiting
-pupilary dilation
Locations of high opiate receptor concentrations
-paleospinothalamic system
-limbic system
-substantia gelatinosa
-solitary, ambiguous, parabrachial nuclei (cough suppression)
-area postrema (nausea vomiting)
-PAG
-GUT
Are opiates a better choice for acute or chronic pain?
Acute
5 indications for opiate prescription
-analgesia
-anesthesia
-cough
-diarrhea
-detoxification
How does morphine cause respiratory depression?
By decreasing responsiveness to pCO2.
6 symptoms which may counterindicate morphine
1) hepatic disease
2) renal disease
3) poor respiratory function
4) head injuries
5) hypotension
6) biliary colic
Morphine (Type/use, admin, excre)
Opioid agonist. Analgesic, administered parenternal or oral, metabolized by hepatic conjugation.
Codine (type/use, admin, abuse)
Use - Opioid agonist. Used with aspirin as as analgesic
Admin - Oral 50% as effective than parenternal. 10% gets converted to morphine which is how it works.
Excre
Abuse - less risk than morphine
Meperidine (type/use, pharm, SE)
Type/use - Opioid agonist. Short duration analgesic, less constipating than morphine)
Pharm - metabolized by liver into convulsant
SE - OD causes stupor and convulsions. IV admin can increase HR
Fentanyl (type/use, pharm, SE)
Type - Opioid agoinst (80x morphine potency). Often used for anesthesia.
Pharm - administered IV or patch,
SE - accumulates with repeated doses
Diphenoxylate (type/use, pharm, SE)
Type - treats diarrhea. Very insoluable, therefore only works in gut. Given with atropine.
Pharm - No central effects at moderate doses.
Methadone (type/use, pharm, SE)
Type - used for addicts, similar to morphine but 85% protein bound.
Pham - given orally, widely spaced intervals
Buprenophine (type/use, pharm, SE)
Type - Used as analgesic, being tested for opiate/cocain addict treatment.
Pharm - 50 times more potent as analgesic, partial mu agonist, kappa antagonist
Pentazocine (type/use, pharm, SE)
Type - Used as analgesic. kappa-sigma agonist, mu antagonist.
Pharm - Given orally, made with naloxone to reduce parenternal abuse.
SE - High dose causes anxiety, nightmares, hallucinations, increases BP and HR. Can cause dependence.
Butorphanol (type/use, pharm, SE)
Same as pentazocine but only available parenternal, does not produce withdrawl syndromes when given to morphine users.
Nalbupine (type/use, pharm, SE)
Same as pentaxocine but without cardiovascular effects.
Naloxone (type/use, pharm, SE)
Type - Opioid mu antagonist. Used for saving life during opioid OD.
SE - none on healthy people, withdrawl on opioid dependent people.
Dextromethorphan (type/use, pharm, SE)
Type - Cough suppressant. Is d isomer of opioid levorphanol but has no other opioid characteristics other than cough suppressant.
SE - Counterindicated in peeps with MAO inhibitors b/c causes excitation and hyperpyrexia.