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25 Cards in this Set
- Front
- Back
Treatment Strategy for Parkinson's (BALSA)
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Bromocriptine (partial dopamine agonist)
Amantidine (causes Dopamine release) Levodopa (converted to dopamine) Selegiline (blocks Dopamine breakdown) Antimuscarinics (benztropine- lowers ACh to relieve rigidity and tremor) |
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L-Dopa/Carbidopa
1)MOA 2)Use 3)Toxicity |
1)L-Dopa crosses BBB and can be converted to Dopamine in the brain by dopa decarboxylase
2) Parkinson's 3) Arrhythmias if converted in periphery, which is blocked by administrating the Carbidopa (blocks peripheral decarboxylase) Also can have dyskinesia after administration and akinesia between doses after long term use |
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Selegiline
1)MOA 2)Use 3)Toxicity |
1) Selectively inhibits MAO-B due decrease breakdown of Dopamine
2)Adjuvant to L-Dopa 3)Can worsen side effects of L-Dopa |
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Sumatriptan
1)MOA 2)Use 3)Toxicity |
1) 5-HT agonist which causes vasoconstriction (very acute with short half life)
2) Acute migraines, cluster headaches 3) Coronary vasospasm, mild tingling. Can't use in Prinzmetal's angina or CAD |
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Seizure Treatments
1) Partial Seizures 2)Tonic Clonic Seziures 3)Absence Seizures 4)Status Epilepticus |
1) All drugs are useful
2)First line is Phenytoin, Carbamazepine, or Valproic Acid 3)First line is Ethosuximide, Valproic Acid will work 4) Prophylaxis is Phenytoin, Acute trt is Benzodiazepines (Diazepam, Lorazaepam) |
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Phenytoin
1)MOA 2)Use 3)Toxicity |
1) Use dependent blockade of Na+ channels, and blocks glutamate release from Excitatory presynaptic terminals
2)Tonic Clonic Seizures, and Class IB antiarrhythmic 3) Diplopia, Ataxia, Nystagmus, SLE-like, induction of p450, gingival hyperplasia, hirsutism, blocks folate absorption (megaloblastic anemia), teratogenic, malignant hyperthermia |
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Carbamazepine
1)MOA 2)Use 3)Toxicity |
1) Blocks Na+ channels
2) Tonic Clonic seizures, Trigeminal Neuralgia 3)Diplopia, Ataxia, induces p450, Agranulocytosis, teratogenic, liver toxicity |
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Gabapentin
1)MOA 2)Use 3)Toxicity |
1)Causes GABA release
2)Tonic Clonic, and peripheral neuropathy 3) Sedation, ataxia |
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Lamotrigine
1)MOA 2)Use 3)Toxicity |
1) Blocks voltage gated Na+ channels
2)Everything but Absence, and Status Epilepticus 3) STEVEN-JOHNSONS RASH |
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Ethosuximide
1)MOA 2)Use 3)Toxicity |
1) Blocks T-type Ca+ Channels
2) Absence seizures 3) Lethargy, Uticaria, Steven Johnsons Rash |
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Valproic Acid
1)MOA 2)Use 3)Toxicity |
1)Inactivates Na+ channels, increases GABA release
2)Everything but Status Epilepticus, and it works in Myoclonic Seizures 3) Hepatotoxic, GI, Spina Bifida, Tremor, Weight Gain |
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Barbituates-Phenobarbital, Pentobarbital, Thiopental
1)MOA 2)Use 3)Toxicity 4)Trt of overdose |
1)increase the duration that the GABA Cl- channel is open --> decrease neuron firing
2) Sedative for anxiety, seizures, insomnia, induction of anesthesia (thiopental) 3) Addictive via dependence, additive CNS depression with EtOH, Respiratory Depression (death), Induction of p450 4) Respiratory Support, BP support |
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Benzodiazepines- Diazepam, Lorazepam, all end in -epam
1)MOA 2)Use 3)Toxicity 4)Trt overdose |
1) Increase frequency of the GABA Cl- channel being open and usually have long half lives (Triazolam, Oxazepam, Midazolam are short TOM)
2)Anxiety, Spasticity, Status Epilepticus, Detox from EtOH, Night Terrors, Sleep Walking (Stage 4 sleep) 3) Dependence, additive depressent with EtOH, but less risk of Respiratory Depression 4)Flumazenil (blocks GABA) |
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Antipsychotics/Neuroleptics - Thioridazine, Haloperidol, Fluphenazine, Chlorpromazine
1)MOA 2)Use |
1)Blocks Dopamine D2 receptors (excess Dopamine implicated in Psychosis and schizophrenia)
2) Schizophrenia,Pychosis, Mania, Tourette's |
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Antipsychotics/Neuroleptics
1)EPS side effects 2)Neuroleptic Malignant Syndrome 3)Tardive Dyskinesia |
1)Blockage of Dopamine in the Basal Ganglia causes the symptoms of
-acute dystonia -akinesia -askathisia -tardive dyskinesia (after 4 mo of therapy Blockage of Dopamine also removes the inhibition of Prolactin --> gynecomastia Muscarinic Block (dry mouth), Hypotension, and sedation (histamine block) 2) Causes rigidity, myoglobinuria, autonomic instability, and hyperexia --> trt with Dantrolene 3) stereotypical oral facial mvmts after long term use |
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Atypical Antipsychotics- Clozipine, Olanzapine, Risperidone
1)MOA 2)Use 3)Toxicity |
1) Blocks Dopamine and 5-HT in diff't tissues
2) Szhizophrenia (both positive and negative symptoms) Olanzapine --> OCD, anxiety, depression, Tourette's mania 3) Few EPS and anticholingergic side effects. Clozapine has Agranulocytosis |
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Lithium
1)MOA 2)Use 3)Toxicity |
1) Completely unknown
2)Mood stabalizer, blocks relapse of manic effects 3)LMNOP Lithium causes Movement problems (tremor) Nephrogenic Diabetes Insipidus hypOthyroidism Pregnancy Problems |
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SSRI's - Fluoxetine, Sertraline, Paroxetine
1)MOA 2)Use 3)Toxicity |
1) Blocks re-uptake of Seratonin
Takes 2-3 weeks to have effect 2) Depression, OCD 3) GI distress, sexual dysfxn (no orgasm) Seratonin Syndrome- happens if on SSRI and MAOi --> hyperthermia, rigid muscles, cardiovascular collapse |
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Tricyclics- imipramine, amitryptaline, desipramine, nortryptiline, clomipramine, doxepin
1)MOA 2)Use 3)Side Effects 4)Toxicity |
1) Block reuptake of NE and Seratonin
2)Major depression, bedwetting (imipramine), OCD (clomipramine) 3)Sedation, Hypotension, Anticholinergic symptoms (amitryptiline) Desipramine is least sedating 4) Tri-C's --> convulsions, Coma, Cardiotoxic May also hallucinate from early anticholinergic side effects |
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Bupoprion
1)Use 2)Toxicity |
1)Depression, Smoking cessation
2) Stimulatory (tachy, insomnia), seizures, no sexual side effects |
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Venlafaxine
1)MOA 2)Use 3)Toxicity |
1)Block Seratonin, NE, and Dopamine reuptake
2) Generalized anxiety, depression 3) Stimulation, nausea, constipation |
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Mirtazapine
1)MOA 2)Use 3)Toxicity |
1)alpha2 blocker --> excess release of NE and Seratonin
2)Depression 3)Sedation, increased appetite, weight gain, increase blood pressure |
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Maprotiline
1)MOA 2)Use 3)Toxicity |
1)Blocks NE reuptake
2)Depression 3)sedation |
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Trazodone
1)MOA 2)Use 3)Toxicity |
1)Blocks 5-HT reuptake
2)Depression 3)Sedation, priapism, hypotension |
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MAOi's - Phenelzine, Tranylcypromine
1)MOA 2)Use 3)Toxicity |
1) Nonselective blockade of MAO --> increases all amine neurotranmitters (Epi, Dopamine, NE)
2)Atypical Depression (with pyschosis), anxiety, hypochondriasis 3) Hypertensive crisis with Tyramine ingestion (Cheese, wine) CNS stimulation, Can't combine with SSRI's or Beta Agonists (Seratonin Syndrome) |