| Term 
 
        | Tension, apprehension, unease |  | Definition 
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        | Overreaction to unknown source or real stimulus |  | Definition 
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        | fear (tachycardia, sweating, trembling, palpations (SAS) |  | 
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        | Types of Anxiety Disorders |  | Definition 
 
        | generalized anxiety disorder specific phobia social phobia (stage fright) panic d/o +/- agoraphobia OCD PTSD |  | 
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        | first true antianxiety drug was.... |  | Definition 
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        | second group of antianxiety was |  | Definition 
 
        | barbiturates more therapeutic but had a low TI |  | 
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        | antianxiety group used more now |  | Definition 
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        | Benzos, ethanol, and barbiturates all have... |  | Definition 
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        | Benzos are inhibitory in nature via.. |  | Definition 
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        | iontropic receptor linked to Cl- channel |  | 
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        | GABA receptor Cl- influx causes |  | Definition 
 
        | hyperpolarization and decreased neuronal firing |  | 
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        | Actions of Benzos in low doses |  | Definition 
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        | actions of benzos in high doses |  | Definition 
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        | MANY (if not all) benzos are... |  | Definition 
 
        | anterograde amnesia  (lose memory from the time you take the drug) |  | 
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        | Term 
 | Definition 
 
        | anticonvulsant activity muscle relaxation, relax spasticity (spinal?) |  | 
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        | Term 
 | Definition 
 
        | autonomic side effects (do not block or stimulate PNS or SAS) antipsychotic actions (do not help/prevent hallucinations) analgesic actions  |  | 
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        | Term 
 | Definition 
 
        | oxazepam triazolam midazolam |  | 
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        | Term 
 
        | famous for its amnestic effect, often used in short duration procedures where you dont want people to remember what is going on |  | Definition 
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        | Intermediate acting benzos |  | Definition 
 
        | alprazolam (xanax) temazepam lorazepam (ativan) |  | 
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        | Term 
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        | popular in the ER, also used as an anticonvulsant agent |  | Definition 
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        | Term 
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        | diazepam (valium( flurazepam clonazepam chloridazapoxide Clorazepate |  | 
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        | Term 
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        | ued exclusively as an anticonvulsant/antieptileptic |  | Definition 
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        | Severe anxiety disorders, what is usually used |  | Definition 
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        | What would be useful for infrequent events (ie a plane trip) |  | Definition 
 
        | short acting benzo can be helpful  Triazolam sometimes beta blockers for refractory cases an SSRI can be given |  | 
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        | drug for muscle relaxation |  | Definition 
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        | drug for chronic epilepsy |  | Definition 
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        | drug for grand-mal seizures (status epilepticus) |  | Definition 
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        | Term 
 | Definition 
 
        | chlordiazepoxide clorazepate diazepam lorazepam oxazepam |  | 
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        | Sleep disorders daytime sedation |  | Definition 
 
        | flurazepam (LA) effective for 4 weeks half-life = 85 hours (risk of OD) |  | 
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        | for frequent awakening slow onset (2-3 hours) |  | Definition 
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        | for problems going to sleep tolerance develops quickly (TAKE ONCE, NOT EVERY DAY) |  | Definition 
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        | Term 
 | Definition 
 
        | decrease sleep induction time decrease number of awakening increase sleep duration |  | 
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        | Rapid tolerance (days) especially... |  | Definition 
 
        | SA morning insomnia daytime anxiety amnesia/confusion |  | 
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        | Term 
 | Definition 
 
        | rebound insomnia use intermittently, use less than 2-4 weeks at a time |  | 
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        | Pharmacokinetics of benzos |  | Definition 
 
        | lipophilic w/ various half lives metabolized in liver metabolites excreted in urine |  | 
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        | Confusion, anxiety, agitation, and insomnia |  | Definition 
 
        | withdrawal symptoms (SA worse) |  | 
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        | Drowsiness, confusion, ataxia, and cognitive impairment |  | Definition 
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 | Definition 
 
        | liver DZ narrow angle glaucoma W/ ETOH and other CNS depressants |  | 
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        | Be aware of the potential for rebound anxiety when using.... |  | Definition 
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        | Benzo antagonist used for rapid reversal of sedation and/or OD IV only |  | Definition 
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        | Benzo withdrawal (anxiety, seizures, sleep d/o, dizziness, N/V, agitation) |  | Definition 
 
        | adverse effects of flumazenil |  | 
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        | Can be used in patients who have problems with dependence |  | Definition 
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        | stimualtes 5HT 1A receptors also DA 2 and 5HT 2A therefore differ from GABA agonists |  | Definition 
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        | minimal sedation, cognitive dyfunction minimal dependence no anticonvulsant no muscle relaxant |  | Definition 
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        | HA, dizziness, nervousness, slow onset of action |  | Definition 
 
        | Adverse effects of buspirone |  | 
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        | antihistamine and antiemtic |  | Definition 
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        | Main action: sedation, common w/ antihistamines little habituation used when history of drug dependence |  | Definition 
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        | Antidepressants First line when concerned about addition/dependence   |  | Definition 
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        | less dependence and adverse effects, can cause withdrawal and be associated w/ the development of tolerance (except Rozarem) |  | Definition 
 
        | other sedative/hypnotic agents Lunesta, Sonata, Ambien, Chloral hydrate |  | 
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        | Acts on subset of benzo site (BZ1) on GABA receptors |  | Definition 
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        |      §  Effective up to 6 months compared to placebo |  | Definition 
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        | Anxiety, dry mouth, chest pain, HA, migraine, edema, unpleasant taste |  | Definition 
 
        | adverse effects of lunesta |  | 
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        | Melatonin MT1 and MT2 receptor agonist Associated w/ maintainence of circadian sleep rhythm promoting circuits in supraschiasmic nucleus |  | Definition 
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        | HA, somnolence, fatigue, dizziness, nausea, insomnia, respiratory infection |  | Definition 
 
        | Adverse effects of Rozarem |  | 
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        | Acts on subset of benzo site (BZ1) on GABA receptors (Me too drug) |  | Definition 
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        |      §  Rapid onset and elimination (half-life = 1 hour), metabolized by CYP3A4 less “hangover” (???) |  | Definition 
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        | Nightmares, agitation, HA, GI upset, dizziness, daytime drowsiness |  | Definition 
 
        | Adverse effects of sonata |  | 
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        | oral spray acts on subset of benzo sites (BZ1) on GABA receptor ME 2 of Sonata |  | Definition 
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        | Replaced by benzos for sedation, induction, and maintainence of sleep |  | Definition 
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        | MOA : increase GABA action of Cl1 thru non-BZ sites block gluatmate receptors and Na+ channels decrease mesencephalic reticular activating system |  | Definition 
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 | Definition 
 
        | CNS depression: sedation, hypnosis, anesthesia NO ANALGESIA (HYPER ANALGESIC) respiratory depression, coma, death induces CYP450 |  | 
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        | Anesthesia barbiturate that has been replaced |  | Definition 
 
        | thiopental  (Pentothal) IV |  | 
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        | Anticonvulsant barbiturate that has been replaced |  | Definition 
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        | Pharmacokinetics of barbiturates |  | Definition 
 
        | IV: Brain > skeletal muscle > adipose absorbed orally metabolized in liver excreted in urine |  | 
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        | Contraindicated in acute intermittent porphyria (expose/exaggerate disease by inducing heme synthesis) |  | Definition 
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        | Non-barbiturate sedatives |  | Definition 
 
        | cloral hydrates antihistamines ETOH   |  | 
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