Mosby's 2014 Nursing Drug Reference (29 page)

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

aluminum hydroxide (OTC)

Func. class.:
Antacid, hypophosphatemic

Chem. class.:
Aluminum product, phosphate binder

ACTION:

Neutralizes gastric acidity; binds phosphates in GI tract, these phosphates are then excreted

USES:

Antacid, hyperphosphatemia in chronic renal failure; adjunct in gastric, peptic, duodenal ulcers; hyperacidity, reflux esophagitis, heartburn, stress ulcer prevention in critically ill, GERD

Unlabeled uses:
GI bleeding

CONTRAINDICATIONS:

Hypersensitivity to product or aluminum products

Precautions:
Pregnancy (C), breastfeeding, geriatric patients, fluid restriction, decreased GI motility, GI obstruction, dehydration, renal disease, sodium-restricted diets

DOSAGE AND ROUTES
Calculator
Antacid

• Adult: PO
600 mg 1 hr after meals, at bedtime, max 6 doses/day

Hyperphosphatemia

• Adult: PO
300-600 mg tid

• Child:
PO
50-150 mg/kg/day in 4-6 divided doses

Available forms:
Susp 320 mg/5 ml, 600 mg/5 ml

Administer:

• 
2 tsp (10 ml) will neutralize 20 mEq of acid

PO route

• 
Hyperphosphatemia: give with 8 oz water, meals unless contraindicated

• 
Laxatives or stool softeners if constipation occurs, especially for geriatric patients

• 
After shaking susp

NG route

• 
By nasogastric tube if patient unable to swallow

SIDE EFFECTS

GI:
Constipation
, anorexia,
obstruction,
fecal impaction

META:
Hypophosphatemia
, hypercalciuria

PHARMACOKINETICS

PO:
Onset 20-40 min, duration 1-3 hr, excreted in feces

INTERACTIONS

Decrease:
effectiveness of—allopurinol, amprenavir, cephalosporins, corticosteroids, delavirdine, digoxin, gabapentin, gatifloxacin, H
2
-antagonists, iron salts, isoniazid, ketoconazole, penicillamine, phenothiazines, phenytoin, quiNIDine, quinolones, tetracyclines, thyroid hormones, ticlopidine, anticholinergics; separate by at least 4-6 hr

Drug/Food

Decrease:
product effect—high-protein meal

Drug/Lab Test

Decrease:
phosphate interference: Tc-99m

NURSING CONSIDERATIONS
Assess:

• 
Pain:
location, intensity, duration, character, aggravating, alleviating factors

• 
Phosphate, calcium levels because product is bound in GI system

• 
Hypophosphatemia: anorexia, weakness, fatigue, bone pain, hyporeflexia

• 
Constipation; increase bulk in diet if needed, may use stool softeners or laxatives; record amount and consistency of stools

• 
Aluminum toxicity:
severe renal disease, may also be used for hyperphosphatemia

Evaluate:

• 
Therapeutic response: absence of pain, decreased acidity, healed ulcers, decreased phosphate levels

Teach patient/family:

• 
Not to use for prolonged periods for patients with low serum phosphate or patients on low-sodium diets, shake liquid well

• 
That stools may appear white or speckled

• 
To check with prescriber after 2 wk of self-prescribed antacid use

• 
To separate from other medications by 2 hr

• 
Hyperphosphatemia:
to avoid phosphate foods (most dairy products, eggs, fruits, carbonated beverages) during product therapy

• 
To notify prescriber black tarry stools, that may indicate bleeding

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

alvimopan

(al-vim′oh-pan)

Entereg

Func. class.:
Functional GI disorder agent

Chem. class.:
Peripheral mu-opioid receptor antagonist

ACTION:

A peripherally selective mu-opioid receptor antagonist with activity restricted to the GI tract

USES:

Prevention of postoperative ileus

Unlabeled uses:
Opiate-agonist–induced constipation

CONTRAINDICATIONS:

Those who have taken therapeutic doses of opioids for more than 7 consecutive days immediately before starting alvimopan, end-stage renal disease, Child–Pugh C

Precautions:
Risk for MI, surgery for complete GI obstruction, hepatic disease, renal disease, pregnancy B, breastfeeding

DOSAGE AND ROUTES
Calculator

• Adult/geriatric patient:
PO
12 mg 30 min-5 hr before surgery, then 12 mg bid beginning the day after surgery; max 7 days or hospital discharge; max 15 doses

Opiate agonist–induced constipation (unlabeled)

• Adult: PO
0.5 mg or 1 mg every day

Renal/hepatic dosage

• Adult: PO
Do not use in end-stage renal disease or Child–Pugh Class C

Available forms:
Cap 12 mg

Administer

• 
Without regard to food

 

Black Box Warning:

Only in a hospital setting approved for the ENTEREG Access Support and Education (E.A.S.E.) program

SIDE EFFECTS

GI:
Constipation, dyspepsia
, flatulence, diarrhea, abdominal pain, cramping

HEMA:
Anemia

META:
Hypokalemia

MISC:
Back pain, urinary retention,
MI

PHARMACOKINETICS

Half-life 10-17 hr, extended in hepatic/renal disease, protein binding 80%-94%

INTERACTIONS

Increase:
Alvimopan concentrations, toxicity—amiodarone, bepridil, cycloSPORINE, diltiazem, itraconazole, quiNIDine, quiNINE, spironolactone, verapamil

• 
Do not us if opiate agonists have been used for 7 consecutive days before alvimopan

• 
Do not use concurrently with other opiate antagonists

NURSING CONSIDERATIONS
Assess:

• 
Blood studies: Hgb/Hct, potassium; hyperkalemia occurs

• 
Recent opioid use, do not use within 7 consecutive days

• 
Opioid use for chronic pain;
MI
is more common in this population

Perform/provide:

• 
Storage at room temperature

Evaluate:

• 
Therapeutic response: Absence of postoperative ileus

Teach patient/family:

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

• 
That product is only used for a limited time in a hospital setting

• 
To report constipation, abdominal pain, cramping

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

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