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89 Cards in this Set
- Front
- Back
procaine
|
-local anesthetic
-ester type |
|
lidocaine
|
-local anesthetic
-amide type |
|
nitrous oxide
|
-general anesthetic
-inhalational |
|
isoflurane
|
-general anesthetic
-inhalational |
|
thiopental
|
-general anesthetic
-parenteral- fast acting barbiturate general anesthetic, sed/hyp |
|
propofol
|
-general anesthetic
-parenteral |
|
ketamine
|
-general anesthetic
-parenteral |
|
vecuronium
|
-muscle relaxant
-non-depolarizing |
|
atracurium
|
-muscle relaxant
-non-depolarizing |
|
succinylcholine
|
-muscle relaxant
-depolarizing |
|
neostigmine
|
-myasthenia gravis
-reversible acetylcholinesterase inhibitor |
|
edrophonium
|
-myasthenia gravis
-reversible acetylcholinesterase inhibitor |
|
morphine
|
-opioid
|
|
codeine
|
-opioid
-prodrug |
|
heroin
|
-opioid
-prodrug |
|
oxycodone
|
-opioid
|
|
naloxone
|
-opioid
-pure antagonist; i.v. only, no oral bioavailability; short half-life |
|
meperidine
|
-opioid
-interaction with MAO inhibitors |
|
diphenoxylate
|
-opioid
-antidiarrheal |
|
methadone
|
-opioid
-long half-life |
|
pentazocine
|
-opioid
-kappa receptor selective agonist; mu receptor partial agonist |
|
dextromethorphan
|
-opioid
-anti-tussive |
|
timolol
|
-glaucoma
-nonselective beta antagonist |
|
betaxolol
|
-glaucoma
-beta 1 - selective antagonist |
|
brimonidine
|
-glaucoma
-alpha 2 - agonist |
|
dipivefrin
|
-glaucoma
-prodrug converted to epinephrine |
|
dorzolamide
|
-glaucoma
-carbonic anhydrase inhibitor |
|
pilocarpine
|
-glaucoma
-nonselective muscarinic agonist |
|
latanoprost
|
-glaucoma
-PGF2 alpha analog |
|
L-DOPA
|
-Parkinson's
-dopamine precursor On-off phenom Wears off 5 years SE= extrapyramidal symptoms pyridoxine(B6) counteracts efficacy |
|
carbidopa
|
-Parkinson's
-peripheral AAD inhibitor -increases L-Dopa potency -decreases peripheral side effects |
|
bromocriptine
|
-Parkinson's
-dopamine receptor agonist (D2) |
|
pramipexole/ropinerole
|
-Parkinson's
-dopamine receptor agonist (D2) -longer duration of action than bromocriptine -good late stage PD tx after L-dopa ineffective -Less on-off and less dyskinesia's than L-dopa |
|
ropinirole
|
-Parkinson's
-dopamine receptor agonist (D2) |
|
entacapone
|
-Parkinson's
-peripheral acting COMT inhibitor ALWAYS used in combo w/ L dopa SE: diarrhea |
|
benzatropine
|
-Parkinson's
-muscarinic receptor antagonist -anti parasympathetic side effects |
|
selegiline
|
-Parkinson's
-MAO-B inhibitor -contraindicated w meperidine or tricyclic antidepressants |
|
chlorpromazine
|
-antipsychotic
-typical, -highly sedative -high muscarinic block (SE) |
|
haloperidol
|
-antipsychotic
-typical; D2 antagonist; -high EPS symptoms -hyperprolatinemia -high potency |
|
aripiprazole
|
-antipsychotic
-atypical; partial D2 agonist, low sedation |
|
clozapine
|
-antipsychotic
-atypical; refractory schizophrenia -most efficacious - risk of agranulocytosis blood monitoring |
|
risperidone
|
-antipsychotic
-atypical; potent D2 blocker -EPS symptoms, tardive dyskinesia, hyperprolactinemia |
|
olanzapine
|
-antipsychotic
-atypical; widely used; -metabolic syndrome |
|
quetiapine
|
-antipsychotic
-atypical; H1 blocker; sedation; weight gain |
|
ziprasidone
|
-antipsychotic
-atypical; mild, prolongs QT interval |
|
diazepam
|
-sed/hyp/anxiolytic
-benzodiazepine - anxiolytic, pre-anesthetic - long acting -anti-convulsant |
|
triazolam
|
-sed/hyp/anxiolytic
-benzodiazepine -sedative-hypnotic, anxiolytic -short half life |
|
alprazolam
|
-sed/hyp/anxiolytic
-benzodiazepine -anxiolytic |
|
lorazepam
|
-sed/hyp/anxiolytic
-benzodiazepine -anxiolytic, epilepsy |
|
flumazenil
|
-sed/hyp/anxiolytic
-benzodiazepine antagonist |
|
zolpidem
|
-sed/hyp/anxiolytic
-unique structure; acts at benzodiazepine site |
|
buspirone
|
-sed/hyp/anxiolytic
-non-benzodiazepine type anxiolytic, - slow onset, - non-sedative |
|
propranolol
|
-sed/hyp/anxiolytic
-anxiolytic, fast acting, non-sedative |
|
phenobarbital
|
-sed/hyp/anxiolytic
-barbituate, anti-epileptic -GABA receptor activation long half life sedation at efficacious doses |
|
diphenhydramine
|
-sed/hyp
-antihistamines (H1 antagonist) |
|
ethanol
|
-drugs of abuse
-depressant |
|
heroin
|
-drugs of abuse
-opioid |
|
nicotine
|
-drugs of abuse
|
|
methamphetamine
|
-drugs of abuse
-sympathomimetic |
|
cocaine
|
-drugs of abuse
-sympathomimetic |
|
caffeine
|
-drugs of abuse
-sympathomimetic |
|
marijuana (THC)
|
-drugs of abuse
-cannabinoid |
|
LSD
|
-drugs of abuse
-psychedelic -decreases serotonin transmission |
|
mescaline
|
-drugs of abuse
-psychedelic -decreases serotonin transmission |
|
phencyclidine (PCP)
|
-drugs of abuse
-psychedelic |
|
MDMA (ecstasy)
|
-drugs of abuse
-designer drug |
|
disulfiram
|
-drugs of abuse
-aversive therapy for alcoholism |
|
varenicline
|
-drugs of abuse
-treatment of nicotine withdrawal -Nicotinic partial agonist |
|
phenytoin
|
-anticonvulsant
-sodium channel blocker -effective against partial and tonic-clonic/grand mal seizures -side effects: nystagmus, diplopia, ataxia gingival hyperplasia/hirsutism/teratogen low therapeutic index zero order kinetics |
|
carbamazepine
|
-anticonvulsant
-sodium channel blocker -drug of choice against partial and tonic-clonic/grand mal seizures -side effects: nystagmus, diplopia, ataxia aplastic anemia/agranulocytosis |
|
lamotrigine
|
-anticonvulsant
-blocks sodium and calcium channels and inhibits glutamate -used for ALL seizure types -skin rash |
|
topiramate
|
-anticonvulsant
-sodium channel blocker modulates GABA receptors and blocks glutamate receptors |
|
valproic acid
|
-tonic clonic and absence
-also used to treat bipolar disorder Decreases GABA turnover -used for all seizure types -hepatotoxicity -teratogen:spina bifida |
|
gabapentin
|
-anticonvulsant
|
|
tiagabine
|
-anticonvulsant
-inhibits GABA transporter GAT-1 |
|
ethosuximide
|
-anticonvulsant
-calcium channel blocker - JUST for petit mal seizure drug of choice for petit mal gastric distress |
|
amitriptyline
|
-antidepressant
-tricyclic -TCAs have risk of cardiac toxicity from slowing conduction -SE: dry mouth, blurry vision, constipation, sedation |
|
nortriptyline
|
-antidepressant
-tricyclic -least sedating of tricyclic drugs -TCAs have risk of cardiac toxicity from slowing conduction; this one can monitor in blood level -SE: dry mouth, blurry vision, constipation, sedation |
|
venlafaxine
|
-antidepressant
-heterocyclic -SNRI (acts on serotonin and NE) -SNRIs used for pain + depression/anxiety, must be tapered due to withdrawal -venlafaxine may increase BP in high doses |
|
bupropion
|
-antidepressant
-heterocyclic -a NE and dopamine reuptake inhibitor -also used for smoking cessation -increased seizure risk in high doses/pts with eating disorders -can worsen anxiety (stimulating) -no sexual side effects |
|
fluoxetine
|
-antidepressant
-SSRI -longest half-life SSRI -SE: N/V, headache, sexual -inhibit P450 enzymes -black box warning increased suicide risk -risk of serotonin syndrome with MAOI |
|
paroxetine
|
-antidepressant
-SSRI -SE: N/V, headache, sexual -inhibit P450 enzymes -black box warning increased suicide risk -risk of serotonin syndrome with MAOI |
|
sertraline
|
-antidepressant
-SSRI -black box warning increased suicide risk -risk of sexual side effects -risk of serotonin syndrome with MAOI |
|
phenelzine
|
-antidepressant
-MAO inhibitor -risk of hypertensive crisis with tyramine rich foods -risk of serotonin syndrome with SSRI |
|
lithium
|
-mood stabilizer
-bipolar disorder -narrow therapeutic range -must maintain adequate sodium to avoid toxicity -monitor levels during pregnancy, no breast feeding |
|
Mirtazapine
|
-alpha 2 antagonist
-in low doses has histaminic actions cause weight gain, sedation -used in frail patients w/ trouble sleeping or low appetite -no sexual side effects |
|
Trazodone
|
-Antidepressant used for insomnia
-SE: Priapism |
|
3 Drugs that can trigger dystonia
|
-metoclopramide (reglan)
-prochlorperazine (compazine) -promethazine (phenergan) |
|
Thioridazine
|
-Antipsychotic
-Typical -Low potency |