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21 Cards in this Set
- Front
- Back
Morpine (Admin, distrib, excretion)
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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. |
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Opiod overdose triad
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coma, pinpoint pupils, depressed respiration.
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Hormonal effects of Morphine
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Increased pituitary release of somatotropin, prolactin, and vasopressin.
Decresed pituitary release of lutenizing hormone causing decreased testosterone and sex drive in males. |
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Opioid withdrawl response
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-lacrimation
-rhinorrhea -perspiration -goose flesh -tremors to frank seizures -anxiety/restless -increased BP and temp -vomiting -pupilary dilation |
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Locations of high opiate receptor concentrations
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-paleospinothalamic system
-limbic system -substantia gelatinosa -solitary, ambiguous, parabrachial nuclei (cough suppression) -area postrema (nausea vomiting) -PAG -GUT |
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Are opiates a better choice for acute or chronic pain?
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Acute
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5 indications for opiate prescription
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-analgesia
-anesthesia -cough -diarrhea -detoxification |
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How does morphine cause respiratory depression?
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By decreasing responsiveness to pCO2.
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6 symptoms which may counterindicate morphine
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1) hepatic disease
2) renal disease 3) poor respiratory function 4) head injuries 5) hypotension 6) biliary colic |
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Morphine (Type/use, admin, excre)
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Opioid agonist. Analgesic, administered parenternal or oral, metabolized by hepatic conjugation.
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Codine (type/use, admin, abuse)
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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 |
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Meperidine (type/use, pharm, SE)
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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 |
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Fentanyl (type/use, pharm, SE)
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Type - Opioid agoinst (80x morphine potency). Often used for anesthesia.
Pharm - administered IV or patch, SE - accumulates with repeated doses |
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Diphenoxylate (type/use, pharm, SE)
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Type - treats diarrhea. Very insoluable, therefore only works in gut. Given with atropine.
Pharm - No central effects at moderate doses. |
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Methadone (type/use, pharm, SE)
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Type - used for addicts, similar to morphine but 85% protein bound.
Pham - given orally, widely spaced intervals |
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Buprenophine (type/use, pharm, SE)
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Type - Used as analgesic, being tested for opiate/cocain addict treatment.
Pharm - 50 times more potent as analgesic, partial mu agonist, kappa antagonist |
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Pentazocine (type/use, pharm, SE)
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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. |
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Butorphanol (type/use, pharm, SE)
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Same as pentazocine but only available parenternal, does not produce withdrawl syndromes when given to morphine users.
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Nalbupine (type/use, pharm, SE)
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Same as pentaxocine but without cardiovascular effects.
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Naloxone (type/use, pharm, SE)
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Type - Opioid mu antagonist. Used for saving life during opioid OD.
SE - none on healthy people, withdrawl on opioid dependent people. |
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Dextromethorphan (type/use, pharm, SE)
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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. |