| Term 
 
        | Antiepileptic 'Phenytonin' Mechanism of Action |  | Definition 
 
        | Inhibits influx of sodium ions thereby reducing excessive firing of cell |  | 
        |  | 
        
        | Term 
 
        | Antiepileptic 'Phenytonin' Indications |  | Definition 
 
        | Psychomotor seizures, status epilepticus |  | 
        |  | 
        
        | Term 
 
        | Antiepileptic 'Phenytonin' Contraindications |  | Definition 
 
        | Sinus bradycardia; SA block; 2nd or 3rd degree AV block |  | 
        |  | 
        
        | Term 
 
        | Antiepileptic 'Phenytonin' Serious Adverse Effects |  | Definition 
 
        | Life-threatening dermatologic reactions; Liver damage; Blood dyscrasias; Cardiovascular collapse if given too rapidly by IV push |  | 
        |  | 
        
        | Term 
 
        | Antiepileptic 'Phenytonin' Common Adverse Effects |  | Definition 
 
        | Dizziness, Ataxia, Blurred vision, Nausea, Gingival hyperplasia; Decreased effectiveness of oral contraceptives and warfarin, decreased blood levels during pregnancy |  | 
        |  | 
        
        | Term 
 
        | Antiepileptic 'Phenytonin' Preadministration assessment |  | Definition 
 
        | Type and frequency of seizure activity; Possibly EKG |  | 
        |  | 
        
        | Term 
 
        | Antiepileptic 'Phenytonin' Monitoring |  | Definition 
 
        | Drug levels (goal is 10-20mcg/ml) |  | 
        |  | 
        
        | Term 
 
        | Antiepileptic 'Phenytonin' Key Patient Education |  | Definition 
 
        | Avoid hazardous activity if CNS depression is significan; Don't stop abruptly (withdrawal seizures); Meticulous oral hygiene; Avoid alcohol/other CNS depressants; Check w/prescriber before starting any other meds |  | 
        |  | 
        
        | Term 
 
        | Antiepileptic 'Phenytonin' Notes |  | Definition 
 
        | Infant death from neonatal hemorrhage (when drug taken by mother)- can be avoided with vitamin K administration |  | 
        |  | 
        
        | Term 
 
        | Tricyclic antidepressant 'Amitriptyline' Mechanism of Action |  | Definition 
 
        | Blocks neuronal uptake of norepinephrine and serotonin |  | 
        |  | 
        
        | Term 
 
        | Tricyclic antidepressant 'Amitriptyline' Indications |  | Definition 
 
        | Depression, Bipolar, chronic pain syndrome, neuropathy, migraine headache, panic disorder, and OCD |  | 
        |  | 
        
        | Term 
 
        | Tricyclic antidepressant 'Amitriptyline' Contraindications |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Tricyclic antidepressant 'Amitriptyline' Serious Adverse Effects |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Tricyclic antidepressant 'Amitriptyline' Common Adverse Effects |  | Definition 
 
        | Drowsiness, Dry mouth, Constipation, Urinary hesitancy, Hypotension |  | 
        |  | 
        
        | Term 
 
        | Tricyclic antidepressant 'Amitriptyline' Preadministration assessment |  | Definition 
 
        | ECG- especially for patients over 40 years of age |  | 
        |  | 
        
        | Term 
 
        | Tricyclic antidepressant 'Amitriptyline' Monitoring |  | Definition 
 
        | Psych symptoms including suicidal ideation |  | 
        |  | 
        
        | Term 
 
        | Tricyclic antidepressant 'Amitriptyline' Key Patient Education |  | Definition 
 
        | Symptom relief not immediate; Change position slowly to minimize orthostasis; Avoid hazardous activities if sedation is significant; Take dose at bed-time to minimize daytime sedation; Avoid alcohol/other CNS depressants; and other anticholinergic agents |  | 
        |  | 
        
        | Term 
 
        | Tricyclic antidepressant 'Amitriptyline' Notes |  | Definition 
 
        | Initial response in 1-3 weeks; full effect over 1-2 months; Continue therapy at least 3 months to prevent relapse |  | 
        |  | 
        
        | Term 
 
        | Selective Serotonin Reuptake Inhibitor 'Sertraline' Mechanism of Action |  | Definition 
 
        | Inhibits CNS reuptake of serotonin, weak effect on dopamine or norepinephrine |  | 
        |  | 
        
        | Term 
 
        | Selective Serotonin Reuptake Inhibitor 'Sertraline' Indications |  | Definition 
 
        | Major depression, OCD, panic disorder, PTSD |  | 
        |  | 
        
        | Term 
 
        | Selective Serotonin Reuptake Inhibitor 'Sertraline' Contraindications |  | Definition 
 
        | Caution in patients with compromised liver function, seizure disorders |  | 
        |  | 
        
        | Term 
 
        | Selective Serotonin Reuptake Inhibitor 'Sertraline' Serious Adverse Effects |  | Definition 
 
        | Seizure, Tachycardia, Bradycardia, AV Block, May increase risk of suicidal thinking or attempts (expecially in pediatric populations); Serotonergic Syndrome (2-72 hrs after treatment)- Agitation, confustion, anxiety, hallucinations, poor concentration, profuse diaphoresis, tremor, fever: resolves when drug discontinued |  | 
        |  | 
        
        | Term 
 
        | Selective Serotonin Reuptake Inhibitor 'Sertraline' Common Advers Effects |  | Definition 
 
        | Decreased libido, Nausea, Headache, Nervousness, Insomnia, Anxiety, Weight gain |  | 
        |  | 
        
        | Term 
 
        | Selective Serotonin Reuptake Inhibitor 'Sertraline' Preadministration Assessment |  | Definition 
 
        | History of seizures; Anxiety, nervousness, insomnia (may be exacerbated); Suicidal ideation |  | 
        |  | 
        
        | Term 
 
        | Selective Serotonin Reuptake Inhibitor 'Sertraline' Monitoring |  | Definition 
 
        | Compare mood to baseline, Assess for suicidal ideation |  | 
        |  | 
        
        | Term 
 
        | Selective Serotonin Reuptake Inhibitor 'Sertraline' Key Patient Education |  | Definition 
 
        | Effects may not be felt for 2-4 weeks; Take with food; Avoid ultraviolet light; Report development of suicidal thoughts or behavior changes; Avoid alcohol and other drugs; Do not stop taking abruptly |  | 
        |  | 
        
        | Term 
 
        | Selective Serotonin Reuptake Inhibitor 'Sertraline' Notes |  | Definition 
 
        | Reaches steady state in 7 days, 94% protein bound; Withdrawal syndrome (dizziness, HA, nausea, sensory disturbances, tremor, anxiety) can be minimized by tapering dose |  | 
        |  | 
        
        | Term 
 
        | Monoamine Oxidase Inhibitor 'Phenelzine' Mechanism of Action |  | Definition 
 
        | Inhibit MAO-A, thereby increasing availability of norepinephrine and serotonin (only partly explains effect- full explanation not yet known) |  | 
        |  | 
        
        | Term 
 
        | Monoamine Oxidase Inhibitor 'Phenelzine' Indications |  | Definition 
 
        | Atypical depression, depression refractory to other therapy, OCD, bulimia (Onset 2-3 weeks) |  | 
        |  | 
        
        | Term 
 
        | Monoamine Oxidase Inhibitor 'Phenelzine' Contraindications |  | Definition 
 
        | Patients taking SSRI's Pheochromacytoma, heart failure, liver disease, severe renal impairment, Cerebrovascular defect, cardiovascular disease, hypertension, age > 60 |  | 
        |  | 
        
        | Term 
 
        | Monoamine Oxidase Inhibitor 'Phenelzine' Serious Adverse Effects |  | Definition 
 
        | Potential for hypertensive crisis (pootentially fatal)- interacts with dietary tyramine, indirect acting sympathomimetic drugs and tricyclic antidepressants; Serotonergic syndrome with SSRIs; Meperidine causes hyperpyrexia |  | 
        |  | 
        
        | Term 
 
        | Monoamine Oxidase Inhibitor 'Phenelzine' Common Adverse Effects |  | Definition 
 
        | Edema, orthostatic hypotension, restlessness, mania or hypomania, blurred vision |  | 
        |  | 
        
        | Term 
 
        | Monoamine Oxidase Inhibitor 'Phenelzine' Preadministration assessment |  | Definition 
 
        | Willingness and ability to adhere to diet and med restrictions; Do not take any Rx or OTC meds w/out consulting w/HCP; Suicidal ideation |  | 
        |  | 
        
        | Term 
 
        | Monoamine Oxidase Inhibitor 'Phenelzine' Monitoring |  | Definition 
 
        | Face to face contact w/patient at least weekly for initial 4 wks; Liver function and CBC every 6 months (leukopenia rare side effect) |  | 
        |  | 
        
        | Term 
 
        | Monoamine Oxidase Inhibitor 'Phenelzine' Key Patient Education |  | Definition 
 
        | S/S of orthostatic hypotension; Risk of hypertensive crisis; Dietary and medication restrictions (required for duration of therapy and 2 weeks after); Do not stop taking abruptly |  | 
        |  | 
        
        | Term 
 
        | Monoamine Oxidase Inhibitor 'Phenelzine' Notes |  | Definition 
 
        | Requires a compliant patient to avoid serious adverse reactions |  | 
        |  | 
        
        | Term 
 
        | Mood stabilizer 'Lithium' Mechanism of Action |  | Definition 
 
        | Unknown, possibly decreases release of norepinephrine and dopamine |  | 
        |  | 
        
        | Term 
 
        | Mood stabilizer 'Lithium' Indications |  | Definition 
 
        | Manic phase of bipolar disease |  | 
        |  | 
        
        | Term 
 
        | Mood stabilizer 'Lithium' Contraindications |  | Definition 
 
        | Severe debilitation, dehydration, sodium depletion, significant CV, renal disease, diurecic use, pregnancy, lactation |  | 
        |  | 
        
        | Term 
 
        | Mood stabilizer 'Lithium' Serious Adverse Effects |  | Definition 
 
        | Toxicity (>1.5 mEq/L)- starts with slurred speech, unsteady gait, weakness, drowsiness, vomiting, diarrhea- can progress to seizure, stupor, irregular heart rhythm and death |  | 
        |  | 
        
        | Term 
 
        | Mood stabilizer 'Lithium' Common Adverse Effects |  | Definition 
 
        | Increased thirst, Frequent urination, Nausea, Fine hand tremor, Hypothyroidism |  | 
        |  | 
        
        | Term 
 
        | Mood stabilizer 'Lithium' Preadministration assessment |  | Definition 
 
        | Fluid and electrolyte balance, Renal function, CV function |  | 
        |  | 
        
        | Term 
 
        | Mood stabilizer 'Lithium' Monitoring |  | Definition 
 
        | Serum lithium levels every 2-3 days during initiation and every 1-3 months during therapy; Annual: CBC, electrolytes, renal function, thyroid function |  | 
        |  | 
        
        | Term 
 
        | Mood stabilizer 'Lithium' Key Patient Education |  | Definition 
 
        | Avoid major changes in sodium and fluid intake, Drink 8-12 glasses of fluid daily; Consult with prescriber before using any other drug- even OTC (especially NSAIDs) |  | 
        |  | 
        
        | Term 
 
        | Mood stabilizer 'Lithium' Notes |  | Definition 
 
        | NSAIDs can increase lithium levels by up to 60%! Levels for acute therapy 0.8-1.4 mEq/L, Levels for maintenance 0.4-1.0 mEq/L)
 |  | 
        |  | 
        
        | Term 
 
        | Benzodiazepine 'Lorazepam' Mechanism of Action |  | Definition 
 
        | Increase effects of GABA (which has inhibitory effect on CNS) |  | 
        |  | 
        
        | Term 
 
        | Benzodiazepine 'Lorazepam' Indications |  | Definition 
 
        | Anxiety, insomnia, seizures, muscle spasms, alcohol withdrawal, anesthesia induction |  | 
        |  | 
        
        | Term 
 
        | Benzodiazepine 'Lorazepam' Contraindications |  | Definition 
 
        | Psychoses, Acute narrow-angle glaucoma, Children <6 months |  | 
        |  | 
        
        | Term 
 
        | Benzodiazepine 'Lorazepam' Serious Adverse Effects |  | Definition 
 
        | Withdrawal symptoms if stopped suddenly; Combining with other CNS depressants can cause respiratory depression, hypotension, bradycardia, altered LOC (can be fatal) |  | 
        |  | 
        
        | Term 
 
        | Benzodiazepine 'Lorazepam' Common Adverse Effects |  | Definition 
 
        | Drowsiness, Ataxia and confusion particularly in older adults, Adverse effects related to CNS depression |  | 
        |  | 
        
        | Term 
 
        | Benzodiazepine 'Lorazepam' Preadministration assessment |  | Definition 
 
        | Fluid and electrolyte balance; Renal function; CV function |  | 
        |  | 
        
        | Term 
 
        | Benzodiazepine 'Lorazepam' Monitoring |  | Definition 
 
        | Tolerance can develop if used longterm (Reversal agent for benzodiazepine is flumazenil- if patient has developed physical dependence could cause acute withdrawal) |  | 
        |  | 
        
        | Term 
 
        | Benzodiazepine 'Lorazepam' Key Patient Education |  | Definition 
 
        | Daily dose split into 2-3 doses for sustained effect. Avoid alcohol, Avoid driving, etc until effects are known; Drowsiness decreases with use |  | 
        |  | 
        
        | Term 
 
        | Benzodiazepine 'Lorazepam' Notes |  | Definition 
 
        | Schedule IV; Effects are limited by intrinsic amount of GABA; Paradoxical reactions of excitement, stimulation and acute rage |  | 
        |  | 
        
        | Term 
 
        | Anxiolytic 'Buspirone' Mechanism of Action |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Anxiolytic 'Buspirone' Indications |  | Definition 
 
        | Short-term treatment of anxiety |  | 
        |  | 
        
        | Term 
 
        | Anxiolytic 'Buspirone' Contraindications |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Anxiolytic 'Buspirone' Serious Adverse Effects |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Anxiolytic 'Buspirone' Common Adverse Effects |  | Definition 
 
        | Dizziness, Nausea, Headache, Nervousness, Light-headedness, Excitement, Tachycardia |  | 
        |  | 
        
        | Term 
 
        | Anxiolytic 'Buspirone' Preadministration assessment and Monitoring |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Anxiolytic 'Buspirone' Key Patient Education |  | Definition 
 
        | Avoid driving, etc if dizzy or drowsy, Do not stop taking abruptly |  | 
        |  | 
        
        | Term 
 
        | Anxiolytic 'Buspirone' Notes |  | Definition 
 
        | Initial response in 1 week, full effect takes several weeks |  | 
        |  |