Mosby's 2014 Nursing Drug Reference (168 page)

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ezetimibe (Rx)

(ehz-eh-tim′bee)

Ezetrol
, Zetia

Func. class.:
Antilipemic; cholesterol absorption inhibitor

ACTION:

Inhibits absorption of cholesterol by the small intestine, causes reduced hepatic cholesterol stores

USES:

Hypercholesterolemia, homozygous familial hypercholesterolemia (HoFH), homozygous sitosterolemia

CONTRAINDICATIONS:

Hypersensitivity, severe hepatic disease

Precautions:
Pregnancy (C), breastfeeding, children, hepatic disease

DOSAGE AND ROUTES
Calculator

• Adult/adolescent/child >10 yr:
PO
10 mg/day; may be given with HMG-CoA reductase inhibitor at same time; may be given with bile acid sequestrant; give ezetimibe 2 hr before or 4 hr after bile acid sequestrant

Available forms:
Tabs 10 mg

Administer:

• 
Without regard to meals

SIDE EFFECTS

CNS:
Fatigue, dizziness, headache

GI:
Diarrhea, abdominal pain

MISC:
Chest pain

MS:
Myalgias, arthralgias
, back pain,
myopathy, rhabdomyolysis

RESP:
Pharyngitis, sinusitis, cough,
URI

SYST:
Angioedema

PHARMACOKINETICS

Metabolized in small intestine, liver; excreted in feces 78%, urine 11%; peak 4-12 hr; half-life 22 hr

INTERACTIONS

Increase:
action of ezetimibe—fibric acid derivatives, cycloSPORINE

Decrease:
action of ezetimibe—antacids, cholestyramine

Drug/Lab Test

Increase:
LFTs

NURSING CONSIDERATIONS
Assess:

• 
Hypercholestrolemia:
diet history: fat content, lipid levels (triglycerides, LDL, HDL, cholesterol); LFTs at baseline, periodically during treatment

• 
Myopathy/rhabdomyolysis:
increased CPK, myalgia, muscle cramps, musculoskeletal pain, lethargy, fatigue, fever; more common when combined with statins

Evaluate:

• 
Therapeutic response: decreased cholesterol, LDL; increased HDL

Teach patient/family:

• 
That compliance is needed

• 
That risk factors should be decreased: high-fat diet, smoking, alcohol consumption, absence of exercise

• 
To notify prescriber if pregnancy suspected, planned or if breastfeeding

• 
To notify prescriber if unexplained weakness, muscle pain present

• 
To notify prescriber of dietary/herbal supplements

Canada only   Side effects:
italics
= common;
bold
= life-threatening   
Nurse Alert

ezogabine

(e-zog′a-been)

Potiga

Func. class.:
Anticonvulsant

ACTION:

The exact mechanism of anticonvulsant effects is not fully known. However, studies indicate that the drug enhances transmembrane potassium currents, which may stabilize the resting membrane potential and reduce brain excitability. May also augment GABA-mediated currents.

USES:

Partial seizures, migraines

CONTRAINDICATIONS:

Hypersensitivity

Precautions:
Suicidal ideation/behavior, prostatic hypertrophy, dementia, psychotic disorders, QT prolongation, congestive heart failure, ventricular hypertrophy, hypokalemia, hypomagnesemia, abrupt discontinuation, renal impairment, hepatic disease, geriatrics pregnancy category C, breastfeeding, neonates, infants, children, adolescents

DOSAGE AND ROUTES
Calculator

• Adult/geriatric patient ≤65 years of age:
PO
Initially, 100 mg tid, increase by ≤50 mg tid per day at weekly intervals depending on response, up to a maintenance dose of 200-400 mg tid depending on response; max is 400 mg tid (1200 mg/day).

• Geriatric patient > 65 years of age:
PO
initially, 50 mg tid, increase by ≤ 50 mg tid per day at weekly intervals depending on response; max 250 mg tid (750 mg/day).

Available forms:
Film-coated tabs 50, 200, 300, 400 mg

Administer:

• 
Tab should be swallowed whole without regard to meals

• 
Give in 3 equally divided doses

SIDE EFFECTS

CNS:
Dizziness, drowsiness, memory impairment, tremor, vertigo, abnormal coordination, disturbance in attention, gait disturbance, aphasia, dysarthria, balance disorder, paresthesias, amnesia, dysphagia, myoclonia, hypokinesia, confusion, anxiety, hallucinations,
suicidal thoughts/behaviors,
fatigue, asthenia, malaise

EENT:
Diplopia, blurred vision

GU:
Urinary retention, hydronephrosis, dysuria, urinary hesitation, hematuria, chromaturia

GI:
Nausea, constipation, dyspepsia, xerostomia, constipation, weight gain, appetite stimulation

MISC:
Influenza, dyspnea,
QT prolongation

MS:
Muscle spasms, weakness

PHARMACOKINETICS

80% protein bound; extensively distributed in the body; extensively metabolized by glucuronidation and acetylation; inactive N-glucuronides are the primary metabolites; elimination half-lives of ezogabine and its N-acetyl metabolite are 7 hr and 11 hr, respectively; 36% excreted renally as exogabine, 18% as NAMR, 24% as the N-glururonides of ezogabine and NAMR, 14% fecal excretion; rapidly absorbed, peak 0.5-2 hr, bioavailability 60%; high-fat food increases peak concentration; increased in hepatic/renal disease, geriatric patients, young adult females

INTERACTIONS:

Increase:
QT prolongation—arsenic trioxide, chloroquine, chlorproMAZINE, mesoridazine thioridazine, clarithromycin, Class IA antiarrhythmics (disopyramide, procainamide, quiNIDine), Class III antiarrhythmics (amiodarone, dofetilide, ibutilide, sotalol), dextromethorphan, dronedarone, droperidol, erythromycin, grepafloxacin, halofantrine, levomethadyl, methadone, pentamidine, pimozide, posaconazole, probucol, propafenone, quiNIDine, saquinavir, sparfloxacin, terfenadine, troleandomycin, ziprasidone

Decrease:
effect of phenytoin

Decrease:
effect of ezogabine—carBAMazepine

Increase:
effect of digoxin

Increase:
urinary retention—antimuscarinics, amantadine, H1-blockers

Increase:
CNS depression—anxiolytics, sedatives, hypnotics, buprenorphine, butorphanol, dronabinol, mirtazapine, nabilone, nalbuphine, opiate agonists, pentazocine, pregabalin, skeletal muscle relaxants, traMADol, traZODone, ethanol

NURSING CONSIDERATIONS
Assess:

 
Seizures:
Assess for type, duration, location, activity, presence of aura

 
QT prolongation:
Monitor in those with known QT prolongation, congestive heart failure, ventricular hypertrophy, hypokalemia, hypomagnesemia, and in patients receiving medications known to cause QT prolongation. QT prolongation can occur within 3 hr of dose

 
Abrupt withdrawal:
Withdraw gradually to minimize increased seizure frequency

 
Suicidal thoughts/behaviors:
Assess for any unusual changes in moods or behaviors, including emotional lability or emerging or worsening depression and suicidal ideation

Teach patient/family:

• 
To avoid driving or operating machinery or performing other tasks that require mental alertness until reaction is known

• 
To avoid concurrent use of alcohol

• 
To avoid abruptly discontinuing this product

 
Suicidal thought/behaviors:
Advise patient to notify prescriber immediately of suicidal thought/behaviors

Canada only   Side effects:
italics
= common;
bold
= life-threatening   
Nurse Alert

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