| Term 
 | Definition 
 
        | SSRIs S/NRIs Tricyclics MAOIs Atypical |  | 
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        | Term 
 | Definition 
 
        | SSRIs S/NRIs Tricyclics MAOIs Atypical |  | 
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        | Term 
 
        | Depression Clinical Features |  | Definition 
 
        | Depressed Mood Loss of pleasure or interest Insomnia Anorexia Mental slowing and loss of concentration Feelings of guilt, worthlessness, helplessness Thoughts of death and suicid Sx must be present most of the day, nearly every day for at least 2 weeks |  | 
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        | Term 
 
        | MAO hypothesis of depression |  | Definition 
 
        | Functional insufficiency of MAO NT (serotonin, DA, NE, epinephrine) |  | 
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        | Term 
 
        | Suicide risk with antidepressants |  | Definition 
 
        | Seen early in treatment (first 6-8 weeks) Rx should be written for the smallest number of doses consistent with good ptnt management. |  | 
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        | Term 
 
        | First choice drug for major depression |  | Definition 
 
        | Tricyclic antidepressants |  | 
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        | Term 
 
        | Tricyclic Antidepressants MOA: Adverse Effects: Most dangerous adverse effects: |  | Definition 
 
        | MOA: Block neuronal reuptake of NE and Serotonin AE: Sedation, orthostatic hypotension, anticholinergic effects, diaphoresis, seizures, hypomania, yawngasm Most dangerous: cardiac toxicity (exacerbates arrhythmias, risk of MI) May increase risk of suicide in early tx |  | 
        |  | 
        
        | Term 
 | Definition 
 
        | Depression Bipolar Other: Neuropathic pain, chronic insomnia, ADHD, Panic disorder, OCD |  | 
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        | Term 
 
        | Tricyclic drug interactions |  | Definition 
 
        | MAOI Direct-acting sympathomimetic Indirect-acting sympathomimetic Anticholinergic agents CNS depressants |  | 
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        | Term 
 
        | Toxicities seen with Tricyclics |  | Definition 
 
        | Dysrrhytmias, Tachycardia, IV blocks, Complete AV block, V tach, V fib |  | 
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        | Term 
 | Definition 
 
        | Gastric lavage Ingestion of activated charcoal Physostigmine Propranolol, lidocaine, phenytoin |  | 
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        | Term 
 
        | Benefit of SSRI vs. tricyclic |  | Definition 
 
        | No hypotension, sedation or anticholinergic effects at normal dosing OD doesn't cause cardiac toxicity so safer for patients with heart problems. Death by OD is extremely rare.  |  | 
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        | Term 
 | Definition 
 
        | Most widely prescribed SSRI |  | 
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        | Term 
 
        | Fluoxetine MOA: Use: Side Effects: Drug Interactions:   |  | Definition 
 
        | MOA: Selective inhibition of Serotonin reuptake   --> CNS excitation Use: OCD, Bulimia, Premenstrual dysphoric disorder SE: Serotonin syndrome (2-72 hours after tx), withdrawal syndrome (agitation, changes in appetite and bp. If you taper dose down you won't get this), Neonatal effects, Teratogenesis (avoid in late stage pregnancy b/c can lead to serotonin syndrome in baby, NT defects seen in animals but not humans), extrapyramidal, bruxism, bleeding, sexual dysfunction, weight gain.  Drug interactions: Warfarin, MAOIs, Tricyclic antidepressants and lithium |  | 
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        | Term 
 
        | Sertraline MOA:  Uses: Side effects: Interactions: |  | Definition 
 
        | MOA: blocks uptake of serotonin and dopamine Uses: major depression, panic disorder, OCD, PTSD, premenstrual dysphoric disorder, social anxiety disorder. Minimal effects on seizure threshold. SE: HA, N, D, Tremor, Insomnia, Weight gain, Agitation, sexual dysfunction, Neonatal abstinence syndrome, premature pulmonary HTN, nervousness. Interactions: MAOIs, Pimozide |  | 
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        | Term 
 
        | Fluvoxamine MOA: Use: Side Effects: |  | Definition 
 
        | MOA: SSRI Use: OCD not depression SE: N,V, constipation, weight gain, dry mouth, HA, sexual dysfunction, abnormal liver function, sedative       |  | 
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        | Term 
 
        | Paroxetine MOA Indications SE |  | Definition 
 
        | MOA: SSRI, shows benefits within a week or 2 Use: major depression, OCD, social phobia, panic, generalized anxiety, PTSD, premenstrual dysphoric disorder. |  | 
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        | Term 
 
        | Citalopram: MOA: Use: Half life: Side effects: |  | Definition 
 
        | MOA: unknown. Doesn't block receptors for serotonin, ach, NE or histamine Use: Major depression Half life: 35 hours SE: Nausea, somnolence, dry mouth, sexual dysfunction, neonatal abstinence syndrome |  | 
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        | Term 
 
        | Escitalopram MOA: Side effects:     |  | Definition 
 
        | MOA: unknown. S-isomer of citalopram but better tolerated Sede effects: Temporary: nausea, insomnia, somnolence, sweating, fatigue |  | 
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        | Term 
 
        | Venlafaxine MOA: Use: Side effects: |  | Definition 
 
        | MOA: SNRI Use: depression, generalized anxiety, social anxiety disorder SE: Nausea, HA, anorexia, nervousness, sweating, somnolence, insomnia, diastolic HTN, sexual dysfunction, hyponatremia (CV problems, arrhythmia, mm pain), neonatal withdrawal syndrome |  | 
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        | Term 
 
        | Duloxetine MOA: Use: PK: SE: Drug interactions:   |  | Definition 
 
        | MOA: SNRI, weakly inhibits dopamine Use: DIABETIC PERIPHERAL NEUROPATHY, depression PK: Food reduces rate of absorption, highly bound to albumin, half life 12 hours SE: Nausea, somnolence, dry mouth, sweating, insomnia Blurred vision,  cross breast milk.  Drug interactions: R'OH, MAOI, Drugs that inhibit CYP1A2 and CYP2D6   |  | 
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        | Term 
 
        | MAOIs can trigger HTN crisis if patient eats food rich in: |  | Definition 
 | 
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        | Term 
 
        | MAOI MOA: Use:  SE: Interactions: |  | Definition 
 
        | MOA: Irreversible inhibition of MAO's. No breakdown of NE, DA, Serotonin. Lasts 2 weeks. Use: Bulimia, OCD, Panic attacks SE: CNS stimulation, orthostatic hypotension, HTN crisis with tyramine (cheese) Interactions: Indirect-acting sympathomimetic agents, Antidepressants, antihypertensive drugs, meperidine (decreases binding of MAOs)   Takes weeks to months to show benefit |  | 
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        | Term 
 | Definition 
 
        | Transdermal MAOI much lower risk of hypertensive crisis  |  | 
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        | Term 
 
        | Bupropion MOA: Use: Benefits: SE: |  | Definition 
 
        | MOA: stimulant an suppress appetite. Does not affect serotonergic, cholinergic or histaminergic transmission Use: depression Benefits: no weight gain, increases sexual desire and pleasure, smoking cessation, quick acting (1-3 weeks) SE: Seizures, Agitation, Tremor, Tachycardia, Blurred vision, dizziness, HA, insomnia, dry mouth, GI upset, constipation, weight loss |  | 
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        | Term 
 | Definition 
 
        | Atypical antidepressant Causes sedation |  | 
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        | Term 
 
        | Electroconvulsive Therapy |  | Definition 
 
        | Tx Depression due to effectiveness, rapid onset Given to ptnts who have failed to respond to drugs or are severely depressed, suicidal. Adverse effect: loss of memory for events immediately surrounding treatment. |  | 
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        | Term 
 | Definition 
 
        | LT therapy of tx resistant depression when at least 4 antidepressant drugs have failed MOA: Stimulates cholinergic release Side effects: hoarseness, voice alteration, cough, dyspnea |  | 
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