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38 Cards in this Set
- Front
- Back
Epinephrine
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MOA: alpha-agonist; vasoconstriction leads to decreased aqueous humor synthesis
tox: mydriasis, stinging contra: closed-angle glaucoma |
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Brimonidine
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MOA: decr aqueous humor synthesis
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Timolol
Betaxolol Carteolol |
MOA: decr aqueous humor secretion
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Acetazolamide
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MOA: carbonic anhydrase inhibitor (decr aq. humor secretion due to decr bicarb)
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Pilocarpine
Carbachol Physostigmine Echothiophate |
MOA: increase humor outflow; contract ciliary muscle to open trabecular meshwork, canal of schlemm (stim. sphincter pupillae of iris--constricts)
use: pilocarpine for emergencies tox: n/v/d, salivation, sweating, miosis, cyclospasm |
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Latanoprost (PGF2alpha)
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MOA: incr aq. humor outflow
tox: browning of iris |
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Opioid analgesics
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MOA: opioid receptor agonists; open K+ channels, close Ca channels (hyperpolarization)
tox: respiratory depression, pinpoint pupils (miosis), CNS depression, constipation reverse: naltrexone (naloxone) |
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Butorphanol
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MOA: partial mu agonist, kappa agonist
tox: withdrawal if were on full opioid agonist before |
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Tramadol
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MOA: very weak opioid agonist; inhibits 5HT and NE reuptake
use: chronic pain tox: decreases seizure threshold |
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Phenytoin
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MOA: incr. Na channel inactivation
use: 1st line tonic-clonic; 1st line for ppx; also for simple/complex tox: nystagmus, diplopia, ataxia, sedation, gingival hyperplasia, hirsutism, megaloblastic anemia, teratogen, SLE-like sxs, cyt P-450 inducer |
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Carbamazepine
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MOA: incr Na channel inactivation
use: first line for tonic-clonic and trigeminal neuralgia; also simple/complex tox: diplopia, ataxia, agranulocytosis, aplastic anemia, liver tox, teratogen, P450 inducer, SIADH |
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Lamotrigine
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MOA: blocks voltage-gated Na and Ca channels
use: simple, complex, t-c tox: Steens-Johnson, HA, dizziness, ataxia |
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Gabapentin
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MOA: incr. GABA
use: simple, complex, t-c, peripheral neuro tox: sedation, ataxia |
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Topiramate
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MOA: blocks Na channels, incr. GABA action
use: simple, complex, t-c tox: sedation, kidney stones, wt. loss, ataxia, teratogen |
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Phenobarbital
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MOA: incr. GABA by incr. duration of Cl channel opening
use: 1st line for pregnant, kids; also s, c, t-c tox: sedation/depr, tol/dep, P450 inducer, vertigo, ataxia, acute psychosis |
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valproic acid
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MOA: incr Na channel inactivation, incr GABA conc.
use: 1st line t-c, absence, s, c, myoclonic tox: GI, hepatotox, neural tube defects, tremor, wt. gain, teratogen, check CBCs |
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Ethosuximide
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MOA: blocks thalamic T-type Ca channels
use: 1st line absence tox: GI, fatigue, HA, urticaria, Stevens-Johnson, aplastic anemia |
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Benzos
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MOA: incr GABA action by incr frequency of Cl channel opening; decr. REM sleep
use: 1st line for acute seizure, eclampsia (MgSO4 is first line), sleepwalking, status epilepticus, anxiety, detox tox: sedation, tolerance, dependence OD: flumazenil (GABA antagonist) |
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(1) Minimum Alveolar Concentration;
(2) Potency |
conc. at which 50% of population is anesthetized (decr with age)
potency = 1/MAC |
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Halothane
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anesthetic
tox: hepatotoxic, malignant hyperthermia |
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Methoxyflurane
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nephrotoxic
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Enflurane
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proconvulsant
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nitrous oxide
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expansion of trapped gas
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Ketamine
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PCP analog; block NMDA receptors; incr. cerebral flow
use: IV anesthetic |
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Propofol
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rapid induction; short procedures
potentiates GABA-a |
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local anesthetics
esters (procaine, cocaine, tetracaine) amides (lidocaine, mepivacaine, bupivacaine) |
MOA: block Na channels; preferentially bind to activated Na channels
order of blockade: small>large; within small/large, meylinated > non order of loss: pain, temp, touch, pressure give with epi tox: CNS, excitation, CV tox, arrhythmia |
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Succinylcholine
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MOA: DEPOLARIZING neuromuscular blocking agent; selective for nicotinic receptor
reversal: cholinesterase inhibitors (neostigmine) tox: hypercalcemia, hyperK |
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Tubocurarine
Atracurium Vecuronium Pancuronium, etc |
MOA: NON depolarizing neuromuscular block; compete with Ach for receptors
Reversal: neostigmine, edrophonium, other cholinesterase inhibitors |
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Dantrolene
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MOA: prevents Ca release from SR of sk. muscle
use: malignant hyperthermia, neuroleptic malignant syndrome |
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Bromocriptine
Pramipexole Ropinirole |
MOA: dopamine agonist
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Amantadine
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MOA: increase dopamine
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Selegiline
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MOA: prevent dopamine breakdown through inhibition of MAO type B
tox: can enhanced adverse effects of L-Dopa |
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Entacapone
tolcapone |
MOA: COMT inhibitors
give with L-dopa/carbidopa |
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Benztropine
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MOA: antimuscarinic; improves tremor and rigidity (no efect on bradykinesia)
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L-DOPA/carbidopa
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L-Dopa converted to dopamine in the CNS
Carbidopa is peripheral decarboxylase inhibitor tox: arrhythmia, can get akinesia btw doses |
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Sumatriptan
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MOA: 5-HT agonist; causes vasoconstriction; inhibits trigeminal activation and casoactive peptide release
tox: coronary vasospasm |
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memantine
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MOA: NMDA antagonist to prevent excitotoxicity
tox: dizziness, confusion, hallucination |
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Donepezil
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MOA: acetylcholinesterase inhibitor (selective for Ach in CNS >>> periphery)
tox: nausea, dizziness, insomnia |