Mosby's 2014 Nursing Drug Reference (368 page)

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

silver nitrate 1%
ophthalmic

 

silver nitrate 1%
sulfacetamide sodium
ophthalmic

 

silver sulfADIAZINE
topical

 

simethicone (
OTC
, Rx)

(si-meth′i-kone)

Barriere
, Equaline Extra Strength Gas Relief, Gas Relief
, Gas-Relief, Gas-X, Good Sense Ultra Strength Gas Relief, Mylanta Gas Relief, Mylanta Gas, Mylicon, Ovol
, Phazyme, Top Care Gas Relief Extra Strength, Walgreens Gas Relief

Func. class.:
Antiflatulent

Do not confuse:
Mylicon
/Mylanta Gas

ACTION:

Disperses/prevents mucus gas pockets in GI system, lowers surface tension of gas bubbles

USES:

Flatulence

Unlabeled uses:
Dyspepsia

CONTRAINDICATIONS:

Hypersensitivity, GI obstruction/perforation

Precautions:
Pregnancy (C), abdominal pain, fistula, hiatal hernia

DOSAGE AND ROUTES
Calculator

• Adult and child >12 yr:
PO
40-125 mg after meals and at bedtime prn, max 500 mg/day

• Child 2-12 yr:
PO
40-50 mg after meals and at bedtime prn, max 240 mg/day

• Child <2 yr:
PO
20 mg qid prn

Available forms:
Chew tabs 40, 150, 166 mg; tabs 60, 80, 95, 125 mg; drops 20 mg/0.3 ml, 95 mg/1.425 ml; caps 95, 180 mg; soft gel caps 125, 180 mg; oral dissolving film 62.5 mg

Administer:

• 
After meals, at bedtime; shake susp well before giving; chew tabs should be chewed

SIDE EFFECTS

GI:
Belching, rectal flatus, diarrhea

NURSING CONSIDERATIONS
Assess:

• 
Reason for excess gas production, decreased bowel sounds, recent surgery, other GI conditions

Evaluate:

• 
Therapeutic response: reduction of abdominal gas, discomfort

Teach patient/family:

• 
That tablets must be chewed

• 
To shake susp well before pouring

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

simvastatin (Rx)

(sim-va-sta′tin)

Zocor

Func. class.:
Antilipemic

Chem. class.:
HMG-CoA reductase inhibitor

Do not confuse:
Zocor
/Cozaar/Zoloft

ACTION:

Inhibits HMG-CoA reductase enzyme, which reduces cholesterol synthesis

USES:

As an adjunct for primary hypercholesterolemia (types IIa, IIb), isolated hypertriglyceridemia (Frederickson type IV) and type III hyperlipoproteinemia, CAD, heterozygous familial hypercholesterolemia

CONTRAINDICATIONS:

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

Precautions:
Past hepatic disease, alcoholism, severe acute infections, trauma, severe metabolic disorders, electrolyte imbalances, Chinese patients

DOSAGE AND ROUTES
Calculator

• Adult:
PO
20-40 mg/day in
PM
initially; usual range 5-40 mg/day in
PM
, max 40 mg/day for most patients, max 80 mg/day for patients taking 80 mg/day chronically without myopathy; dosage adjustments may be made in ≥4-wk intervals; those taking verapamil and amiodarone max 20 mg/day; max <80 mg for Chinese patients taking lipid-modifying niacin doses

• Child/adolescent ≥10 yr including girls ≥1 yr postmenarche:
PO
10 mg in
PM
, range 10-40 mg/day

With diltiazem/verapamil/dronedarone

• Adult:
PO
5-10 mg in
PM
, max 10 mg/day

With amiodarone, amolodipine, ranolazine

• Adult:
PO
5-20 mg daily in evening, max 20 mg/day

Heterozygous familial hypercholesterolemia

• Adolescent 10-17 yr:
PO
10 mg/day, max 40 mg/day

Available forms:
Tabs 5, 10, 20, 40, 80 mg

Administer:

• 
Total daily dose in evening

SIDE EFFECTS

CNS:
Headache, cognitive impairment

GI:
Nausea, constipation, diarrhea, dyspepsia, flatus, abdominal pain,
liver dysfunction, pancreatitis,
hyperglycemia

INTEG:
Rash, pruritus

MS:
Muscle cramps, myalgia,
myositis, rhabdomyolysis,
myopathy

RESP:
Upper respiratory tract infection

PHARMACOKINETICS

Metabolized in liver (active metabolites); >98% protein bound; excreted primarily in bile, feces (60%), kidneys (15%); peak 1-2 hr; half-life 3 hr

INTERACTIONS

 
Do not use with cycloSPORINE, gemfibrozil

 
Increase:
effects of warfarin

 
Increase:
rhabdomyolysis, myalgia; do not use concurrently—niacin, erythromycin, clofibrate, clarithromycin, ketoconazole, itraconazole, protease inhibitors, macrolide antibiotics, danazol, delavirdine, nefazodone, verapamil, diltiazem, amiodarone, azole antifungals, telithromycin, voriconazole

Increase:
serum level of digoxin

Drug/Herb

Increase:
effect—red yeast, rice

Decrease:
effect—St. John’s wort

Drug/Lab Test

Increase:
CK, LFTs

NURSING CONSIDERATIONS
Assess:

• 
Diet history: fat consumption; baseline and lipid profile: LDL, HDL, TG, cholesterol

• 
Hepatic studies at baseline, after 4-6 wk, periodically thereafter; AST, ALT, may increase

 
Rhabdomyolysis:
muscle tenderness, increased CPK levels (10× above upper normal limit); therapy should be discontinued, more likely in those receiving >80 mg/day, first year of treatment, those ≥65 yr, females

• 
Renal studies in patients with compromised renal systems: BUN, I&O ratio, creatinine

Perform/provide:

• 
Storage in cool environment in tight container protected from light

Evaluate:

• 
Therapeutic response: decrease in LDL, total cholesterol, triglycerides; increase in HDL; slowing CAD

Teach patient/family:

• 
That blood work will be necessary during treatment

• 
To report severe GI symptoms, headache

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

• 
To notify prescriber if pregnancy is suspected or planned; pregnancy (X); not to breastfeed

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