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JESSICA
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which of the following is not a clinical application of benzodiazepines
a. acute anxiety states
b. general anxiety disorder
c. skeletal muscle relaxation
d. seizure disorder
e. insomnia
f. Parkinson
f. parkinson
L27 anxiety and sleep disorder
which of the following is not a benzodiazepine drug
a. alprazom
b. clonazepam
c. lorazepam
d. diazepam
e. triazopam
e. triazopam
(made up)
L27 anxiety and sleep disorder
A patient is taking alprazolam (benzodiazepine) for panic attacks but took too many and is now overdosing on it. What is the antidote drug to reverse these effects?
a. midazolam
b. flumazenil
c. zolpidem
d. butabarbital
b. flumazenil
antidote for OD on benzo
L27 anxiety and sleep disorder
name the drug class that has this MOA: bind to GABAa receptor subunit to facilitate chloride opening and increase frequency
a. benzodiazepines
b. benzothiazines antagonist
c. hypnotics
d. H1 receptors
a. benzodiazepines
L27 anxiety and sleep disorder
Lipid soluble drugs enter the central nervous system
a. fast
b. slow
a. fast
L27 anxiety and sleep disorder
some drugs have active metabolites with long half life which can accumlate and cause excess sedation. this is problematic for which age group
a. infants
b. teenagers
c. elderly
d. new parents
c. elderly
L27 anxiety and sleep disorder
which neurotransmitter is most assoicated with inhibition in the CNS
a. norepineprhine
b. serotonin
c. GABA
d. dopamine
c. GABA
L27 anxiety and sleep disorder
where does GABA bind on the ion channel
a. between alpha and gamma
b. between alpha and beta
c. within the membrane channel
d. goes through the chloride channel
b. between alpha and beta
where is GABAa NOT located
a. thalamus
b. limbic structures
c. cerebellar cortex
d. cerebral cortex
c. cerebellar cortex
where does benzodiazepines bind
a. between alpha and gamma
b. between alpha and beta
c. between a1 and y2 subunits
d. goes through the chloride channel
c. between a1 and y2 subunits
benzodiazepines binding facilitates the inhibitory actions of GABA by:
a. decreased frequency of GABA chloride ion channel opening
b. increased frequency of GABA chloride ion channel opening
c. constant frequency of GABA chloride ion channel opening
d. membrane hypo polarization
b. increased frequency of GABA chloride ion channel opening
what is the drug used to reverse benzodiazepine and its CNS affects
a. flumazenil
b. gaba agonist
c. norepinephrine
d. noxolone
a. flumazenil
which of the following is the inverse agonist of benzodiazepine which have high affinity for BZ receptors.
a. acarbose
b. a-carboline
c. lispro
d. fluconazole
b. a-carboline
which of the following drug class MOA is to increase the duration of GABA-mediated chloride ion channel opening
a. barbituates
b. benzodiapenes
c. new hypnotics
d. zolpidems
a. barbituates
barbituates can or cannot be reversed by flumazenil
a. can
b. cannot
cannot
because uses different binding sites
which of the following is not considered one of the "z" drugs
a. zolpidem
b. zaleplon
c. eszopiclone
d. zaditor
d. zaditor
true or false: Z drugs interact with certain benzo receptors
true; still not considered a benzo drug tho
can the effects Z drugs be reversed by flumazenil?
a. yes
b. no
a. yes; since it interacts with certain benzo receptors
where do benzo bind on the GABAA receptor
a. between B and Y subunits
b. between a and b subunits
c. between a and y subunits
d. between a and a subunits
c. between a and y subunits
which of the following best describes the mechanism of sedative action of benzo
a. activate GABAb receptors in the spinal cord
b. stimulate release of GABA from nerve endings in the brain
c. increase frequency of opening chloride ion channels associated with GABAa receptors
d. inhibit GABA transaminase to increase brain levels of GABA
c. increase frequency of opening chloride ion channels associated with GABAa receptors
Flumazenil will counteract the action of each of the following drugs except:
a. alprazolam
b. buspirone
c. diazepam
d. eszopiclone
b. buspirone
which drugs are classified as selective for the GABAa receptor isoform containing a1 subunit
a. benzodiazepines
b. barbiturates
c. zolpidem, zaleplon, eszopiclone
d. baclofen
c. zolpidem, zaleplon, eszopiclone
what is the primary mechanism by which benzo enhance GABA effect
increase duration of channel opening
flumazenil acts as an antagonist at which receptor
benzo
which drug class is preferred for rapid control of panic attacks
a. beta blockers
b. eszopiclone
c. benzodiazepines
d. zolpidem
c. benzodiazepines
which of the following benzo drugs have greater long term efficacy for panic and phobic disorders (select 2)
a. alprazolam
b. clonazepam
c. diazepam
d. zaleplon
a. alprazolam
b. clonazepam
which medical condition has seen an incresing use of newer antidepressants for treatment, as opposed to traditional benzos
a. acute anxiety states
b. chronic anxiety states
c. insomnia
d. muscle spasticity
b. chronic anxiety states
a 40 year old woman has occasional acute attacks of intense anxiety with marked physical symptoms, including hypertension, tachycardia, and sweating. if she is diagnosed as suffering from panic disorder, the most appropriate drug to use is: (select 2)
a. alprazolam
b. eszopiclone
c. flurazepam
d. propranolol
e. clonazepam
a. alprazolam
e. clonazepam
what is a primary concern regarding the use of ebnzo in older patients
a. overdose risk
b. increased heart rate
c. greater sensitivity to CNS depressant effects
d. high potential for addiction
c. greater sensitivity to CNS depressant effects
among the following drugs, which is noted for having minimal effects on sleep patterns and less daytime cognitive impairment compared to traditional benzo
a. flurazepam
b. diazepam
c. zolpidem
d. midazolam
c. zolpidem
sedative hypnotic drugs are generally not recommended for which of the following sleep disorders
a. insomnia
b. sleep apnea
c. parasomnia
d. circadian rhythm disorders
b. sleep apnea
long acting benzo are primarily used in the manage of withdrawal states in individuals dependent on which substance
a. opioids
b. cocaine
c. ethanol
d. stimulants
c. ethanol
which antidepressant primarily exert their effects through antagonism of the 5-HT2A receptor
a. SSRI
b. Tricyclic antidepressants
c. nefazodone and trazodone
d. monamine oxidase inhibitors
C. nefazodone and trazodone
which of the following drugs is most likely to be of value in obsessive compulsive disorders
a. amitripyline
b. bupropion
c. fluoxetine
d. trazodone
e. venlafaxine
c. fluoxetine