Neuro Additional ATI Charts – Flashcards

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pramipexole (Mirapex)
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Relieves symptoms of Parkinson's disease; restless leg syndrome
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Drug classification for pramipexole (Mirapex)
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direct-acting dopamine receptor agonists
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Side effects of pramipexole (Mirapex)
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Nausea and other GI symptoms; drowsiness; "SLEEP ATTACKS"; muscle weakness; orthostatic hypotension; DYSKINESIAS (abnormal muscle movements)
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Precautions for pramipexole (Mirapex)
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renal dysfunction; existing compulsive behaviors; children
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Interactions with pramipexole (Mirapex)
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cimetidine increases levels; metoclopramide and phenothiaine antipsychotics decrease therapeutic effect; alcohol and other CNS depressants increase risk for adverse effects
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Interventions for pramipexole (Mirapex)
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monitor for nausea; monitor for drowsiness or sudden sleepiness and keep patient safe from accidents; monitor for muscle weakness and prevent falls; monitor blood CPK levels if weakness occurs; monitor cardiac status; observe for abnormal muscle movement/dyskinesia (tremors, etc)
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Patient instructions for pramipexole (Mirapex)
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Take with food if nausea occurs; if taking once daily, take before bedtime; report muscle weakness to provider; notify provider if dyskinesias occur; if pramipexole is discontinued, taper dosage slowly over 1 week
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thiopental (Pentothal)
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rapid induction of anesthesia and hypnosis for brief procedures; adjunct anesthesia with other agents for procedures less than 15 minutes
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Drug classification of thiopental (Pentothal)
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general anesthesia/barbiturate
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Administration of pramipexole (Mirapex)
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Give 3 hr before bedtime for restless leg syndrome; when increasing dosage, allow 4 to 7 days between each increase
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Administration of thiopental (Pentothal)
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available for IV injection or infusion only; assure that intra-arterial or vein extravasation do not occur
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Side effects of thiopental (Pentothal)
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respiratory depression (apnea with large doses); cardiovascular toxicity--tachycardia, hypotension
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Contraindications for thiopental (Pentothal)
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hepatic porphyria; history of paradoxical excitation with use of CNS depressants; STATUS ASTHMATICUS
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Interventions for thiopental (Pentothal)
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monitor respiratory status carefully during/after use; monitor VS before/during/after use
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Precautions for thiopental (Pentothal)
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hepatic or renal disease; myasthenia gravis; chronic respiratory d/o's; severe anemia; cardiac disease
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Patient Instructions for thiopental (Pentothal)
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Advise patient that frequent monitoring will occur before, during, and following procedure
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Interactions with thiopental (Pentothal)
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Use with other CNS depressants may increase respiratory depression; use with probenecid may increase length of anesthesia; herbal kava kava and valerian increase sedative properties; multiple incompatibilities in solution with other drugs; use with general benzodiaepine anesthetics, such as midazolam (Versed), is considered duplicate therapy, resulting in prolonged anesthesia
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midazolam (Versed)
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sedation before general anesthesia; conscious sedation with induction of amnesia during procedures, such as endoscopy; supplement to inhalation anesthesia for surgeries
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Classification of midazolam (Versed)
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general anesthesia/benzodiazepine
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Administration of midazolam (Versed)
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may administer IM into large muscle mass for conscious sedation; Give IV bolus or infusion for induction of anesthesia or conscious sedation; DO NOT GIVE BOLUS TO NEONATES; may combine with an opioid for conscious sedation
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Side effects of midazolam (Versed)
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AMNESIA (memory loss from time prior to injection); cardiac or respiratory arrest
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Contraindications for midazolam (Versed)
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pregnancy category D; lactation; obstetric delivery; glaucoma
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Precautions for midazolam (Versed)
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Parkinson's disease, other neuromuscular disorders; cardiac, pulmonary, or renal disorders
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Interventions for midazolam (Versed)
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To prevent cardiac/respiratory arrest, inject IV bolus slowly and wait at least 2 minutes before giving a second dose; have resuscitation equipment at hand; monitor VS carefully during and after procedure
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Patient instructions for midazolam (Versed)
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Advise patient that memory loss was caused by the drug; advise patient that frequent monitoring will occur before, during, and after procedure
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Interactions with midazolam (Versed)
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CNS depressants, anticonvulsants increase sedation from midazolam; cimetidine may cause midazolam toxicity; smoking decreases sedative effect herbal products may increase or decrease effect of midazolam
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fentanyl (Sublimaze)
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supplement to general anesthesia; used with droperidol, and nitrous oxide for neuroleptanesthesia; used with skeletal muscle relaxant as anesthesia for high risk patients in selected situations
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Administration of fentanyl (Sublimaze)
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available in multiple forms for surgical premedication, including IV and stick lozenges; Place a stick lozenge between cheek and gum of child or adult; patient should suck (NOT CHEW) on lozenge longer than 15 minutes
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Side effects of fentanyl (Sublimaze)
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sedation; nausea; respiratory and/ or circulatory depression
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Contraindications for fentanyl (Sublimaze)
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substance abuse; obstetric delivery; myasthenia gravis
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Interventions for fentanyl (Sublimaze)
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monitor LOC during use; monitor for nausea; monitor VS carefully; have resuscitation equipment at hand; have the opioid antagonis, NALOXONE (NARCAN) available
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Patient instructions for fentanyl (Sublimaze)
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advise patient that drowsiness is expected; instruct patient to report nausea; advise patient that frequent monitoring will occur before, during, and after procedure
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Precautions for fentanyl (Sublimaze)
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patients with increased intracranial pressure; older adults or young children; debilitated patients; cardiac or respiratory disorders liver or kidney disorders
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Interactions for fentanyl (Sublimaze)
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MAOI antidepressants given within 2 weeks of fentanyl can cause hypertensive crisis; CNS depressants increase risk for sedation, respiratory depression
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lidocaine (Xylocaine)
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Use: provides local anesthesia-topical application to skin to relieve burns or during suturing of wounds-relives pain in mucous membranes of nose, mouth-relieves pain of hemorrhoids; IV regional anesthesia; blocks nerves near surgical field; injected for epidural or spinal anesthesia
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classification of lidocaine (Xylocaine)
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local anesthesia
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Administration of lidocaine (Xylocaine)
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avoid eyes with topical form; do not apply to broken skin (increase risk of toxicity); assure that correct concentration and form are used for specific procedure; addition of epinephrine to lidocaine increases time of anesthesia but may cause GANGRENE in end-artery sites, such as fingers, toes, nose; some forms contain preservatives which are contraindicated for certain procedures
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Side effects of lidocaine (Xylocaine)
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hypotension (spinal anesthesia); CNS stimulant effects-dizziness, restlessness, tremors, confusion, paresthesias, convulsions, and cardiac conduction disorders; CNS depressant effects-respiratory arrest
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Interventions for lidocaine (Xylocaine)
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monitor VS carefully during/after procedure; if hypotension occurs, lower the head of bed; prepare to administer ephedrine or phenylephrine if hypotension occurs; monitor for CNS effects during/following procedure monitor respiratory status carefully
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Patient instructions for lidocaine (Xylocaine)
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Advise patient to expect careful monitoring of VS during and after procedure; advise patient to report dizziness, paresthesia, breathing difficulty during/after procedure
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Contraindications for lidocaine (Xylocaine)
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sepsis or severe trauma; bradycardia or heart block
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Precautions for lidocaine (Xylocaine)
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older adults; myasthenia gravis; respiratory depression; history of malignant hyperthermia
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Interactions with lidocaine (Xylocaine)
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beta blockers, cimetidine, quinidine increases lidocaine levels; phenytoin increases risk of cardiac effects procainamide increases risk for CNS and cardiac effects
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memantine (Namenda)
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Use: slows decrease in functioning for-moderate/severe Alzheimer's disease; mild/moderate vascular dementia
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Administration of memantine (Namenda)
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available orally in tablets or liquid solution; give with or without food
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Side effects of memantine (Namenda)
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CNS effects: dizziness, headache, increased confusion; constipation
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Interventions for memantine (Namenda)
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monitor for CNS effects; keep patient safe if dizziness occurs; monitor for constipation
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Contraindications for memantine (Namenda)
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renal failure
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Patient instructions for memantine (Namenda)
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Report presence of CNS effects to provider; Increase fluids and fiber in diet; Report constipation to provider
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Precautions for memantine (Namenda)
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liver disorders; renal disorders; seizure disorders; older adults
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Interactions with memantine (Namenda)
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OTC antacids and other drugs that increase pH of urine cause increased levels of memantine and possible toxicity; memantine with levodopa/carbidopa can enhance the adverse effects of levodopa/carbidopa; other NMDA antagonists, such as amantadine or ketamine may increase memantine levels
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dantrolene (Dantrium)
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Use: relaxes skeletal muscle spasm in CVA, stroke, spinal cord injury, MS, cerebral palsy; used to prevent and treat malignant hyperthermia
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Administration of dantrolene (Dantrium)
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available in oral and IV preparations; for prophylaxis of malignant hyperthermia, give orally for 1 to 2 preoperatively; IV form is used to treat malignant hyperthermia
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Side effects of dantrolene (Dantrium)
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muscle weaknss; drowsiness, dizziness; diarrhea; liver toxicity
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Classification of dantrolene (Dantrium)
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peripherally acting muscle relaxants
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Interventions of dantrolene (Dantrium)
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assess muscle strength frequently during treatment; monitor for CNS effects, such as drowsiness; oral dantrolene may be started at low doses and gradually increased to prevent CNS effects; monitor for diarrhea, especially early in treatment; monitor liver function tests
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Patient instructions for dantrolene (Dantrium)
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instruct patient to inform provider if muscle weakness occurs; instruct patient to avoid driving and activities that require mental alertness if drowsiness occurs; advise patients to avoid CNS depressants, such as alcohol, while taking dantrolene; Contact provider if diarrhea occurs; report signs of liver dysfunction, such as abdominal pain, jaundice to provider
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Contraindications for dantrolene
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liver disease
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Precautions for dantrolene
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cardiac disease; pulmonary disease; neuromuscular disorders; patients older than 35 years
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Interactions with dantrolene
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estrogen use increases risk of liver toxicity in women older than 35 years; CNS depressants, such as alcohol, increases risk for excessive sedation; IV use: calcium channel blockers increase risk for severe cardiac dysrhythmias
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Classification of sumatriptan (Imitrex)
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serotonin agonist
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sumatriptan (Imitrex)
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Use: relieve symptoms of existing migraine or cluster headache
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Administration of sumatriptan (Imitrex)
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give orally, SC, or by nasal spray; use nasal spray by spraying once into a single nostril; may repeat every 2 hours; single dose ranges from 5 to 20 mg; maximum dose is 40 mg in 24 hr; give one SC injection repeat once after 1 hr if no relief; no more than 2 doses in 24 hr; give one oral tablet; repeat once after 2 hr if no relief; singe dose ranges from 25 to 100 mg; maximum dose is 200 mg in 24 hr
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Side effects of sumatriptan (Imitrex)
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CHEST PRESSURE OR "HEAVINESS" may progress to angina pain caused by coronary vasospasm; CNS effects: tingling sensation, vertigo
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Interventions for sumatriptan (Imitrex)
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monitor for chest pressure; monitor VS closely after first dose; monitor for CNS effects
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Patient instructions for sumatriptan (Imitrex)
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Notify provider at once for chest pressure or tightness/heaviness in back, jaw, throat that does not spontaneously resolve; instruct patient to report CNS symptoms to provider at next visit
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Contraindications for sumatriptan (Imitrex)
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CAD, angina, previous MI, severe HTN; PVD; older adults; older adults; stroke; use of MAOI within last 2 weeks; use of another triptan within last 24 hrs
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Precautions for sumatriptan (Imitrex)
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liver or kidney insufficiency; CAD risk factors; seizure d/o; BP elevation; serotonin syndrome; chest, jaw, or neck tightness; fertility impairment
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Interactions with sumatriptan (Imitrex)
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MAOI taken within 2 weeks can cause sumatriptan toxicity; ergotamine or another triptan patients use within 24 hour of sumatriptan increases chance of angina; serotonin agonists with sumatriptan can cause serotonin syndrome; herbal St. John's wort can cause toxicity
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interferon beta-1a (Avonex, Rebif); beta-1b (Betaseron): IMMUNOMODULATORS
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Use: Beta-1a: MS (relapsing-remitting type) Beta-1b: MS (relapsing and relapsing-remitting types)
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Administration of interferon beta-1a
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Avonex: Give IM weekly Rebif: Give SC daily for 3 days each week; admin late in day; allow 48 hrs between injection
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Administration beta-1b
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Betaseron: Give SC every other day; use within hours of reconstituting
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Side effects of interferon beta-1a and beta-1b
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FLU-LIKE SYMPTOMS (decrease with prolonged treatment); MYELOSUPPRESSION (all blood cell types); liver toxicity; pain, redness at SC injection site
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Interventions for interferon beta-1a and beta-1b
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begin with low dose and titrate to higher doses to prevent adverse effects; medicate with acetaminophen or other prescribed NSAID if symptoms are expected (flu-like symptoms); monitor CBC and liver function tests before treatment begins and periodically thereafter; monitor for injection site reactions
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Patient instructions for interferon beta-1a and beta-1b
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instruct patient to pre-medicate with prescribed NSAID if flu-like symptoms occur; notify provider for easy bruising, bleeding, fatigue; report abdominal tenderness, anorexia, jaundice to provider; rotate injection sites, use cool compress prior to injection and warm, moist compress following injection; report skin ulceration to provider
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Contraindications for interferon beta-1a and beta-1b
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previous allergy to interferon beta, human albumin, or mannitol
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Precautions for interferon beta-1a and beta-1b
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SUICIDAL TENDENCIES; pre-existing or history or liver disorder; alcohol abuse; children younger than 18 years seizures; mental health disorder; thyroid disorders
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Interactions with interferon beta-1a and beta-1b
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any drug which suppresses the immune system (prednisone) may increase risk for myelosupression
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selegiline (Eldepryl, Zelapar ODT): Indirect-acting Dopamine Receptor Agonists/MAOI
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Uses: symptoms of Parkinson's disease as an adjunct to levodopa/carbidopa; major depression-transderma patch (Emsam)
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Administration of selegiline
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Give with levodopa/carbidopa so that levodopa dosage may be reduced; give orally disintegrating form (Zelapar) by placing it on the top of the tongue; give before morning meal; don't eat or drink for 5 minutes before or after administration
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Side effects of selegiline
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insomnia, HTN (as an interaction with other drugs), orthostatic hypotension; IRRITATION OF ORAL MUCOUS MEMBRANES (with orally-disintegrating form); HALLUCINATIONS
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Interventions for selegiline
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monitor for insomnia; carefully monitor other drugs patient may be taking; monitor BP while taking this drug; monitor orthostatic BP and pulse; inspect tongue and oral cavity for irritation; monitor for hallucinations
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Patient teaching for selegiline
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Take last dose of the day by noon to prevent insomnia; notify provider before taking any new medication; instruct patient about foods to avoid (tyramine foods); inform patient of drugs, including herbals, which may interact with selegiline; rise slowly from lying or sitting position; report oral irritation; educate patient about risk of hallucinations and report if this occurs
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Contraindications for selegiline
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uncontrolled HTN; suicidal ideations; receiving meperidine for pain; concurrent use with dextromthorphan, other MAOIs, meperidine, methadone, or tramadol
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Precautions for selegiline
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HTN; bipolar disorder or psychosis; lactation
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Interactions with selegiline
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meperidine (Demerol) and other opioids, other MAOIs, TCA or SSRI antidepressants can cause high fever, HTN, rigidity; foods containing tyramine can cause HTN; herbal drugs, such as ephedra, St. John's wort, ginseng, or ma huang can cause severe HTN; antihypertensive drugs, diuretics or general anesthetics can cause hypotension
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