Mosby's 2014 Nursing Drug Reference (249 page)

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

loxapine (Rx)

(lox′a-peen)

Loxapac
, Loxitane

Func. class.:
Antipsychotic, neuroleptic

Chem. class.:
Dibenzoxazepine

Do not confuse:
Loxitane
/Soriatane

ACTION:

Depresses cerebral cortex, hypothalamus, limbic system, which control activity and aggression; blocks neurotransmission produced by DOPamine at synapse; exhibits strong α-adrenergic, anticholinergic blocking action; mechanism for antipsychotic effects is unclear

USES:

Psychotic disorders, nonpsychotic symptoms associated with dementia

Unlabeled uses:
Depression, anxiety

CONTRAINDICATIONS:

Hypersensitivity, blood dyscrasias, coma, brain damage, bone marrow depression, alcohol and barbiturate withdrawal states, severe CNS depression, closed-angle glaucoma

Precautions:
Pregnancy (C), breastfeeding, children <16 yr, geriatric patients, seizure disorders, cardiac/renal/hepatic disease, prostatic hypertrophy, cardiac conditions

 

Black Box Warning:

Increased mortality in elderly patients with dementia-related psychosis

DOSAGE AND ROUTES
Calculator

• Adult:
PO
10 mg bid-qid initially, may be rapidly increased depending on severity of condition, maintenance 60-100 mg/day

• Geriatric:
PO
5-10 mg daily-bid, increase q4-7days by 5-10 mg, max 250 mg/day

Available forms:
Caps 5, 10, 25, 50 mg; tabs 5, 10, 25, 50 mg; conc 25 mg/ml

Administer:

• 
Reduced dose to geriatric patients

• 
Anticholinergic agent if EPS symptoms occur

PO route

• 
Concentrate mixed in orange or grapefruit juice

SIDE EFFECTS

CNS:
EPS: pseudoparkinsonism, akathisia, dystonia, tardive dyskinesia, drowsiness, headache
,
seizures,
confusion,
neuroleptic malignant syndrome

CV:
Orthostatic hypotension
,
cardiac arrest,
ECG changes, tachycardia

EENT:
Blurred vision, glaucoma

GI:
Dry mouth, nausea, vomiting, anorexia, constipation
, diarrhea, jaundice, weight gain

GU:
Urinary retention, urinary frequency, enuresis, impotence, amenorrhea, gynecomastia

HEMA:
Anemia, leukopenia, leukocytosis, agranulocytosis

INTEG:
Rash
, photosensitivity, dermatitis

RESP:
Laryngospasm,
dyspnea,
respiratory depression

PHARMACOKINETICS

Metabolized by liver, excreted in urine, crosses placenta, enters breast milk, initial half-life 5 hr, terminal half-life 19 hr

PO:
Onset 20-30 min, peak 2-4 hr, duration 12 hr

INTERACTIONS

Increase:
toxicity—EPINEPHrine

Increase:
EPS—other antipsychotics

Increase:
CNS depression—MAOIs, antidepressants, alcohol

Increase:
anticholinergic effects—anticholinergics

Decrease:
effects—guanadrel, guanethidine, levodopa

Drug/Herb

Increase:
CNS depression—chamomile, cola tree, hops, kava, nettle, nutmeg, skullcap, valerian

Increase:
EPS—betel palm, kava

NURSING CONSIDERATIONS
Assess:

• 
Mental status before initial administration

• 
Swallowing of PO product; check for hoarding, giving of product to other patients

• 
I&O ratio; palpate bladder if low urinary output occurs, urinary retention may be present

• 
Bilirubin, CBC, LFTs q mo

• 
Urinalysis recommended before and during prolonged therapy

• 
Affect, orientation, LOC, reflexes, gait, coordination, sleep-pattern disturbances

• 
B/P standing and lying; pulse, respirations q4hr during initial treatment; establish baseline before starting treatment; report drops of 30 mm Hg

• 
Dizziness, faintness, palpitations, tachycardia on rising

• 
EPS
including akathisia (inability to sit still, no pattern to movements), tardive dyskinesia (bizarre movements of jaw, mouth, tongue, extremities), pseudoparkinsonism (rigidity, tremors, pill rolling, shuffling gait)

 
Neuroleptic malignant syndrome:
muscle rigidity, increased CPK, altered mental status, hyperthermia

• 
Constipation, urinary retention daily; if these occur, increase bulk, water in diet

Perform/provide:

• 
Supervised ambulation until stabilized on medication; do not involve patient in strenuous exercise program because fainting is possible; patient should not stand still for long periods

• 
Increased fluids to prevent constipation

• 
Sips of water, candy, gum for dry mouth

• 
Storage in airtight, light-resistant container

Evaluate:

• 
Therapeutic response: decrease in emotional excitement, hallucinations, delusions, paranoia; reorganization of patterns of thought, speech

Teach patient/family:

• 
That orthostatic hypotension may occur; to rise from sitting or lying position gradually

• 
To avoid hot tubs, hot showers, tub baths because hypotension may occur; that, in hot weather, heat stroke may occur; to take extra precautions to stay cool

• 
To avoid abrupt withdrawal of product because EPS may result; that product should be withdrawn slowly

• 
To avoid OTC preparations (cough, hay fever, cold) unless approved by prescriber; that serious product interactions may occur; to avoid use with alcohol, CNS depressants; that increased drowsiness may occur

• 
To avoid hazardous activities until stabilized on medication

• 
To use sunscreen during sun exposure to prevent burns

• 
About necessity for meticulous oral hygiene because oral candidiasis may occur

• 
To report impaired vision, jaundice, tremors, muscle twitching

TREATMENT OF OVERDOSE:

Lavage; provide an airway, do not use EPINEPHrine

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

lubiprostone (Rx)

(loo-bee-pros′tone)

Amitiza

Func. class.:
Gastrointestinal agent —miscellaneous

ACTION:

Locally acting chloride channel activator; enhances a chloride-rich intestinal fluid secretion without altering other electrolytes; increases motility in the intestine, thereby increasing softening and passage of stool

USES:

Chronic idiopathic constipation, constipation-predominant irritable bowel syndrome in women >18 yr

CONTRAINDICATIONS:

Hypersensitivity, GI obstruction

Precautions:
Pregnancy (C), breastfeeding, children, diarrhea, inflammatory bowel disease, abdominal pain, cholelithiasis, fecal impaction, GI/hepatic disease

DOSAGE AND ROUTES
Calculator
Chronic idiopathic constipation

• Adult:
PO
24 mcg bid with food, water

IBS with constipation (females)

• Adult and adolescent ≥18 yr:
PO
8 mcg bid with food, water

Hepatic dose

• Adult:
PO For chronic constipation:
16 mcg bid (Child-Pugh B); 8 mcg bid (Child-Pugh C);
for irritable bowel:
8 mcg daily (Child-Pugh C), may be increased if tolerated

Available forms:
Caps 8, 24 mcg

Administer:

• 
With food bid

SIDE EFFECTS

CNS:
Headache
, dizziness, depression, fatigue, insomnia

CV:
Hypertension, chest pain

GI:
Nausea, abdominal pain, eructation
, abdominal distention, constipation, diarrhea, dry mouth, dyspepsia, flatulence, gastroenteritis viral, gastroesophageal reflux disease, vomiting, fecal incontinence, fecal urgency

GU:
UTI

MISC:
Chest pain, peripheral edema, influenza, pyrexia, viral infection

MS:
Back pain, arthralgia, muscle cramps, pain in extremities

RESP:
Bronchitis, cough, dyspnea, nasopharyngitis, sinusitis, upper respiratory tract infection

PHARMACOKINETICS

Peak 1.14 hr; 94% protein binding; half-life 0.9-1.4 hr; metabolism rapid, extensively in stomach, jejunum

INTERACTIONS

Decrease:
effect by antidiarrheals and anticholinergics

• 
Do not use with sodium phosphate monobasic monohydrate, sodium phosphate dibasic anhydrous or with other laxative, purgatives when evacuating bowel prior to radiologic exam or surgery

• 
Possible GI obstruction: NIFEdipine ext rel tab

NURSING CONSIDERATIONS
Assess:

• 
GI symptoms:
nausea, abdominal pain, diarrhea

• 
Need for continued treatment periodically

Perform/provide:

• 
Storage at room temp

Evaluate:

• 
Therapeutic response: decreased constipation

Teach patient/family:

• 
To notify prescriber of GI symptoms, diarrhea, hypersensitivity reactions

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