Mosby's 2014 Nursing Drug Reference (362 page)

BOOK: Mosby's 2014 Nursing Drug Reference
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rosuvastatin (Rx)

(roe-soo′va-sta-tin)

Crestor

Func. class.:
Antilipemic

Chem. class.:
HMG-CoA reductase inhibitor

ACTION:

Inhibits HMG-CoA reductase enzyme, which reduces cholesterol synthesis

USES:

As an adjunct for primary hypercholesterolemia (types IIa, IIb) and mixed dyslipidemia, elevated serum triglycerides, homozygous/heterozygous familial hypercholesterolemia (FH), slowing of atherosclerosis, CV disease prophylaxis

Unlabeled uses:
MI, stroke prophylaxis (normal LDL)

CONTRAINDICATIONS:

Pregnancy (X), breastfeeding, hypersensitivity, active hepatic disease

Precautions:
Children, geriatric patients, past hepatic disease, alcoholism, severe acute infections, trauma, hypotension, uncontrolled seizure disorders, severe metabolic disorders, electrolyte imbalances, severe renal impairment, hypothyroidism, Asian patients

DOSAGE AND ROUTES
Calculator
Hypercholesterolemia

• Adult:
PO
5-40 mg/day; initial dose 10 mg/day, reanalyze lipid levels at 2-4 wk, adjust dosage accordingly

Homozygous familial hypercholesterolemia

• Adult:
PO
20 mg/day, max 40 mg

Dose in patients taking cycloSPORINE/gemfibrozil/lopinavir/ritonavir/atazanavir

• Adult:
PO
5 mg/day, max 10 mg/day

Asian patients/patients with predisposition for myopathy

• Adult:
PO
5 mg/day

Atherosclerosis slowing

• Adult:
PO
10 mg/day (for those not taking cycloSPORINE or gemfibrozil)

Heterozygous familial hypercholesterolemia

• Females ≥1 yr postmenarche and ≥10 yr):
PO
5-20 mg/day individualized

MI/stroke prophylaxis (unlabeled)

• Adult:
PO
20 mg daily

Renal/hepatic dose

• Adult:
PO
CCr <30 ml/min, 5 mg/day; max 10 mg/day; avoid use with hepatic disease

Available forms:
Tabs 5, 10, 20, 40 mg

Administer:

• 
May be taken at any time of day, with/without food

SIDE EFFECTS

CNS:
Headache, dizziness
, insomnia, paresthesia

GI:
Nausea, constipation, abdominal pain, flatus, diarrhea, dyspepsia, heartburn
,
kidney failure, liver dysfunction,
vomiting

HEMA:
Thrombocytopenia, hemolytic anemia, leukopenia

INTEG:
Rash, pruritus

MS:
Asthenia, muscle cramps, arthritis, arthralgia, myalgia
,
myositis, rhabdomyolysis;
leg, shoulder, or localized pain

RESP:
Rhinitus, sinusitis,
pharyngitis
, increased cough

PHARMACOKINETICS

Peak 3-5 hr, minimal live metabolism (about 10%), 88% protein bound, excreted primarily in feces (90%), crosses placenta, half-life 19 hr, not dialyzable

INTERACTIONS

Increase:
hepatotoxicity—alcohol

Increase:
rosuvastatin effect—bile acid sequestrants

 
Increase:
myalgia, myositis, rhabdomyolysis—cycloSPORINE, gemfibrozil, niacin, clofibrate, azole antifungals, antiretroviral protease inhibitors, fibric acid derivatives

Increase:
bleeding risk—warfarin

Drug/Lab Test

Increase:
LFTs

NURSING CONSIDERATIONS
Assess:

• 
Diet; obtain diet history including fat, cholesterol in diet

• 
Fasting cholesterol, LDL, HDL, triglycerides at baseline and q4-6wk, then periodically

• 
Liver function: LFTs at baseline, 12 wk, then q6mo; AST, ALT, LFTs may increase

• 
Renal function in patients with compromised renal system: BUN, creatinine, I&O ratio

 
Rhabdomyolysis:
muscle pain, tenderness, obtain CPK; if these occur, product may need to be discontinued; for patients with Asian ancestry: increased blood levels, rhabdomyolysis

Perform/provide:

• 
Storage in cool environment in airtight, light-resistant container

Evaluate:

• 
Therapeutic response: decreased LDL, cholesterol, triglycerides, increased HDL, slowing CAD

Teach patient/family:

 
To report suspected pregnancy; to use contraception while taking product, pregnancy category (X); not to breastfeed

 
To report weakness, muscle tenderness, pain, fever; liver injury (jaundice, anorexia, abdominal pain)

• 
That blood work and follow-up exams will be necessary during treatment

• 
To report severe GI symptoms, dizziness, headache, muscle pain, weakness

• 
That previously prescribed regimen will continue: low-cholesterol diet, exercise program, smoking cessation

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

rufinamide (Rx)

(roo-fin′a-mide)

Banzel

Func. class.:
Anticonvulsant

Chem. class.:
Triazole derivative

ACTION:

May act through action at sodium channels; exact action is unknown

USES:

Lennox-Gastaut syndrome

Unlabeled uses:
Partial seizures

CONTRAINDICATIONS:

Hypersensitivity, familial short QT syndrome

Precautions:
Pregnancy (C), breastfeeding, children <16 yr, geriatric patients, renal/hepatic disease, depression, dialysis, hazardous activities, suicidal ideation

DOSAGE AND ROUTES
Calculator

• Adult:
PO
400-800 mg/day divided bid, increase by 400-800 mg/day q2days to 3200 mg/day

• Child ≥4 yr:
PO
10 mg/kg/day divided equally bid; increase by 10 mg/kg/day every other day to 45 mg/kg/day or 3200 mg/day, whichever is less

Available forms:
Tabs 200, 400 mg; oral susp 40 mg/ml

Administer:

• 
PO tabs:
give with food; may give whole, crushed, or halved

• 
Oral susp:
shake well before use, use provided adapter and calibrated oral dosing syringe, insert adapter firmly in neck of bottle before use, keep in place for duration of bottle use; insert dosing syringe into adapter, withdraw dose from inverted bottle; replace cap after each use, use within 90 days of opening, give with food

SIDE EFFECTS

CNS:
Dizziness, ataxia, drowsiness, fever, seizures, tremor, fatigue, headache, gait disturbance

EENT:
Diplopia, blurred vision, nystagmus

GI:
Nausea, hepatitis, vomiting

HEMA:
Anemia, leukopenia, neutropenia, thrombocytopenia,
lymphadenopathy

INTEG:
Rash, urticaria

MISC:
Edema, hematuria, influenzae, nephrolithiasis

PHARMACOKINETICS

Peak 4-6 hr, half-life 6-10 hr, metabolized by liver, excreted by kidneys, 34% protein binding

INTERACTIONS

Increase:
rufinamide effect—valproate

Decrease:
effect of hormonal contraceptives

Decrease:
effect of rufinamide—carBAMazepine, phenytoin, primidone, PHENobarbital

Drug/Lab Test

Increase:
LFTs

NURSING CONSIDERATIONS
Assess:

• 
Seizures:
duration, type, intensity precipitating factors

 
Mental status: mood, sensorium, affect, memory (long, short), increased suicidal thoughts/actions

Evaluate:

• 
Therapeutic response: decrease in severity of seizures

Teach patient/family:

• 
Not to discontinue product abruptly because seizures may occur

• 
To avoid hazardous activities until stabilized on product

• 
To carry emergency ID stating product use

• 
To notify prescriber if pregnancy is planned or suspected; to use alternative form of contraception because effect of hormonal contraceptives may be decreased

• 
To consume adequate fluids

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