Mosby's 2014 Nursing Drug Reference (231 page)

BOOK: Mosby's 2014 Nursing Drug Reference
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Canada only   Side effects:
italics
= common;
bold
= life-threatening   
Nurse Alert

lacosamide (Rx)

(la-koe′sa-mide)

Vimpat

Func. class.:
Anticonvulsant

Chem. class.:
Functionalized amino acid

ACTION:

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

USES:

Adjunctive therapy for partial seizures

CONTRAINDICATIONS:

Hypersensitivity

Precautions:
Pregnancy (C), breastfeeding, children <17 yr, geriatric patients, allergies, cardiac/renal/hepatic disease, acute MI, atrial fibrillation/flutter, AV block, bradycardia, CHD, dehydration, depression, dialysis, hazardous activity, electrolyte imbalance, heart failure, labor, PR prolongation, sick sinus syndrome, substance abuse, suicidal ideation, syncope, torsades de pointes

DOSAGE AND ROUTES
Calculator

• Adult and adolescent ≥17 yr:
PO
50 mg bid, may increase weekly by 100 mg bid to 200-400 mg/day;
IV
50 mg bid, infuse over 30-60 min, may be increased by 100 mg/day weekly up to 200-400 mg/day maintenance

Renal/hepatic dose

• Adult:
PO/IV
max 300 mg/day for mild to moderate hepatic disease or CCr ≤30 ml/min

Available forms:
Film-coated tabs 50, 100, 150, 200 mg; IV 20 ml single-use vials (200 mg/20 ml); oral sol 10 mg/ml

Administer:
PO route

• 
Tablet:
give without regard to meals

• 
Oral sol:
measure with calibrated measuring device

IV route

• 
May give undiluted or mixed in 0.9%NaCl, D
5
, or LR

• 
Infuse over 30-60 min

• 
Do not use if discolored or if particulates are present; discard unused portions

SIDE EFFECTS

CNS:
Dizziness, syncope, tremor, vertigo, ataxia, drowsiness, fever, hypoesthesia, paresthesias, depression, fatigue, headache, confusion, irritability, psychologic dependence,
suicidal ideation

CV:
Atrial fibrillation/flutter, AV block, bradycardia, myocarditis, orthostatic hypotension, palpitations, PR prolongation

EENT:
Diplopia, blurred vision, nystagmus, tinnitus

GI:
Nausea, constipation, vomiting,
hepatitis,
diarrhea, dyspepsia

HEMA:
Anemia, neutropenia

INTEG:
Rash, erythema, inj site reaction, pruritus, xerostomia

MS:
Asthenia, dysarthria

SYST:
Drug reaction with eosinophilia, systemic symptoms (DRESS)

PHARMACOKINETICS

Metabolized by liver; excreted by kidneys, 95%; protein binding <15%

PO:
Peak 1-4 hr

IV:
Peak 30-60 min; half-life 13 hr; elimination half-life 15-23 hr

INTERACTIONS

 
Increase:
PR prolongation—beta-blockers, calcium channel blockers, atazanavir, dronedarone, digoxin, lopinavir, ritonavir

 
Increase:
lincosamide effect—CYP2C19 inhibitors (fluconazole, isoniazid, miconazole)

Drug/Lab Test

Increase:
LFTs

NURSING CONSIDERATIONS
Assess:

• 
Seizures:
duration, type, intensity precipitating factors

• 
Renal function: albumin concentration

• 
CV status: orthostatic hypotension, PR prolongation; monitor cardiac status throughout treatment

• 
Mental status: mood, sensorium, affect, memory (long, short term), depression, suicidal ideation, psychologic dependence

• 
Rash, hypersensitivity reactions

• 
Pregnancy:
Enroll in UCB Antiepileptic Drugs Registry 1-888-537-7734

Perform/provide:

• 
Storage of PO products/IV vials at room temp; sol is stable for 24 hr when mixed with compatible diluents in glass or PVC bags at room temp

Evaluate:

• 
Therapeutic response: decrease in severity of seizures

Teach patient/family:

• 
Not to discontinue product abruptly; to taper over 1 week because seizures may occur

• 
To avoid hazardous activities until stabilized on product

• 
To carry emergency ID stating product use

• 
To notify prescriber of suicidal thoughts/behaviors, syncope, cardiac changes

• 
To notify prescriber if pregnancy is planned or suspected

• 
That interactions with other medications may occur

• 
To consult MedGuide for proper use, risks

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

lactulose (Rx)

(lak′tyoo-lose)

Constulose, Enulose, Generlac, Kristalose

Func. class.:
Laxative; ammonia detoxicant (hyperosmotic)

Chem. class.:
Lactose synthetic derivative

ACTION:

Prevents absorption of ammonia in colon by acidifying stool; increases water, softens stool

USES:

Chronic constipation, portal-systemic encephalopathy in patients with hepatic disease

CONTRAINDICATIONS:

Hypersensitivity, low-galactose diet

Precautions:
Pregnancy (B), breastfeeding, geriatric patients, debilitated patients, diabetes mellitus

DOSAGE AND ROUTES
Calculator
Constipation

• Adult:
PO
15-30 ml/day (10-20 g), may increase to 60 ml/day prn

• Child:
PO
7.5 ml/day

Hepatic encephalopathy

• Adult:
PO
30-45 ml (20-30 g) tid or qid until stools soft;
RETENTION ENEMA
300 ml (200 g) diluted

• Child:
PO
40-90 ml/day in 3-4 divided doses

• Infant:
PO
2.5-10 ml/day in divided doses

Available forms:
Oral sol (encephalopathy) 10 g/15 ml; oral sol (constipation) 10 g/15 ml

Administer:
PO route

• 
With 8 oz fruit juice, water, milk to increase palatability of oral form; for rapid effect, give on empty stomach

• 
Increased fluids to 2 L/day; do not give with other laxatives; if diarrhea occurs, reduce dosage

• 
Kristalose:
dissolve contents of packet/4 oz water

Rectal route

• 
Retention enema
by diluting 300 ml lactose/700 ml of water; administer by rectal balloon catheter

SIDE EFFECTS

GI:
Nausea, vomiting, anorexia, abdominal cramps
, diarrhea, flatulence, distention, belching

META:
Hypernatremia

PHARMACOKINETICS

Metabolized in colon, excreted by kidneys, onset 1-2 days, peak unknown, duration unknown

INTERACTIONS

• 
Do not use with other laxatives (hepatic encephalopathy)

Increase:
GI obstruction—NIFEdipine ext-rel tabs

Decrease:
lactulose effects—neomycin, other oral antiinfectives, antacids

Drug/Herb

Increase:
laxative action—flax, senna

Drug/Lab Test

Increase:
blood glucose (diabetic patients)

Decrease:
blood ammonia

NURSING CONSIDERATIONS
Assess:

• 
Stool:
amount, color, consistency

• 
Cause of constipation;
determine whether fluids, bulk, or exercise is missing from lifestyle; use of constipating products

• 
Hepatic encephalopathy:
blood ammonia level (30-70 mg/100 ml); may decrease ammonia level by 25%-50%; clearing of confusion, lethargy, restlessness, irritability if portal-systemic encephalopathy

• 
Blood, urine electrolytes if product used often; may cause diarrhea, hypokalemia, hyponatremia

• 
I&O ratio to identify fluid loss

• 
Cramping, rectal bleeding, nausea, vomiting; if these symptoms occur, product should be discontinued

Evaluate:

• 
Therapeutic response: decreased constipation, decreased blood ammonia level, clearing of mental state

Teach patient/family:

• 
Not to use laxatives long term

• 
To dilute with water or fruit juice to counteract sweet taste

• 
To store in cool environment; not to freeze

• 
To take on an empty stomach for rapid action

• 
To report diarrhea; may indicate overdose

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