Mosby's 2014 Nursing Drug Reference (428 page)

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

zolpidem (Rx)

(zole′pih-dem)

Ambien, Ambien CR, Edluar, Zolpimist

Func. class.:
Sedative/hypnotic

Chem. class.:
Imidazopyridine

 

Controlled Substance Schedule IV
ACTION:

Produces CNS depression at limbic, thalamic, hypothalamic levels of CNS; may be mediated by neurotransmitter γ-aminobutyric acid (GABA); results are sedation, hypnosis, skeletal muscle relaxation, anticonvulsant activity, anxiolytic action

USES:

Insomnia, short-term treatment; insomnia with difficulty of sleep onset/maintenance (ext rel)

CONTRAINDICATIONS:

Hypersensitivity to benzodiazepines

Precautions:
Pregnancy (C), breastfeeding, children <18 yr, geriatric patients, anemia, renal/hepatic disease, suicidal individuals, drug abuse, psychosis, seizure disorders, angioedema, depression, respiratory disease, sleep apnea, sleep-related behaviors (sleepwalking), myasthenia gravis

DOSAGE AND ROUTES
Calculator

• Adult:
PO
5 mg (women), 5-10 mg (men) at bedtime × 7-10 days only; total max dose 10 mg;
EXT REL
6.25 (women), 6.25-12.5 mg (men) immediately before bedtime, may be useful for ≤24 wk in people 18-64 yr with primary insomnia;
oral spray
(Zolpimist) 5 mg (women), 5-10 mg (men) immediately before bedtime, max 10 mg/day;
SL
(Edluar) 5 mg (women), 5-10 mg (men) just before bedtime

• Geriatric:
PO
5 mg at bedtime;
EXT REL
6.25 mg; SL: 5 mg at bedtime

Available forms:
Tabs 5, 10 mg; ext rel tabs 6.25, 12.5 mg; SL: 5, 10 mg; oral spray 5 mg/spray

Administer:
PO route

• 
Do not break, crush, or chew ext rel

• 
Take with full glass of water

• 
½-1 hr before bedtime (PO); right before retiring (ext rel)

• 
On empty stomach for fast onset; may be taken with food if GI symptoms occur

Spray route

• 
Prime before first use or if pump is not used for ≥14 days

• 
Do not use spray with or after a meal

Sublingual route

• 
Separate blister pack at perforation, peel paper and push product through, place product under tongue, allow to dissolve before swallowing; do not take with water

SIDE EFFECTS

CNS:
Headache, lethargy, drowsiness, daytime sedation, dizziness, confusion, lightheadedness, anxiety, irritability, amnesia, poor coordination, complex sleep-related reactions (sleep driving, sleep eating), depression, somnolence,
suicidal ideation,
abnormal thinking/behavioral changes

CV:
Chest pain, palpitations

GI:
Nausea, vomiting, diarrhea, heartburn, abdominal pain, constipation

HEMA:
Leukopenia, granulocytopenia (rare)

MISC:
Myalgia

SYST:
Severe allergic reactions, angioedema, anaphylaxis

PHARMACOKINETICS

PO:
Onset up to 1.5 hr, metabolized by liver, excreted by kidneys (inactive metabolites), crosses placenta, excreted in breast milk, half-life 2-3 hr

INTERACTIONS

Increase:
action of both products—alcohol, CNS depressants

Increase or decrease:
zolpidem levels—CYP3A4 inhibitors/inducers

Decrease:
zolpidem effect—rifamycins

NURSING CONSIDERATIONS
Assess:

 
Mental status: mood, sensorium, affect, memory (long, short term), excessive sedation, impaired coordination,
suicidal thoughts/behaviors

• 
Blood dyscrasias: fever, sore throat, bruising, rash, jaundice, epistaxis (rare)

• 
Type of sleep problem: falling asleep, staying asleep

Perform/provide:

• 
Storage in tight container in cool environment

Evaluate:

• 
Therapeutic response: ability to sleep at night, decreased amount of early morning awakening if taking product for insomnia

Teach patient/family:

• 
That dependence is possible after long-term use

 
That complex sleep-related behaviors may occur (sleep driving/eating)

• 
To avoid driving or other activities requiring alertness until dosage is stabilized

• 
To avoid alcohol ingestion

• 
That effects may take 2 nights for benefits to be noticed

• 
Not to use during pregnancy, breastfeeding

• 
That hangover is common in geriatric patients but less common than with barbiturates; that rebound insomnia may occur for 1-2 nights after discontinuing product; not to discontinue abruptly; to taper

• 
Not to crush, chew, break ext rel tabs

• 
To prime spray pump before using

TREATMENT OF OVERDOSE:

Lavage, activated charcoal; monitor electrolytes, VS

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

zonisamide (Rx)

(zone-is′a-mide)

Zonegran

Func. class.:
Anticonvulsant

Chem. class.:
Sulfonamides

ACTION:

May act through action at sodium and calcium channels, but exact action is unknown; serotonergic action

USES:

Epilepsy, adjunctive therapy for partial seizures

Unlabeled uses:
Bipolar disorder (mania)

CONTRAINDICATIONS:

Hypersensitivity to this product or sulfonamides; psychiatric condition, hepatic failure

Precautions:
Pregnancy (C), breastfeeding, children <16 yr, geriatric patients, allergies, renal/hepatic disease

DOSAGE AND ROUTES
Calculator

• Adult and child >16 yr:
100 mg/day, may increase after 2 wk to 200 mg/day, may increase q2wk, max dose 600 mg/day

Available forms:
Caps 25, 50, 100 mg

SIDE EFFECTS

CNS:
Dizziness, insomnia, paresthesias, depression, fatigue, headache, confusion, somnolence, agitation, irritability, speech disturbance,
suicidal ideation, seizures, status epilepticus

EENT:
Diplopia, verbal difficulty, speech abnormalities, taste perversion, amblyopia, pharyngitis, rhinitis, tinnitus, nystagmus

GI:
Nausea, constipation, anorexia, weight loss, diarrhea, dyspepsia, dry mouth, abdominal pain

GU:
Kidney stones

HEMA:
Aplastic anemia, granulocytopenia
(rare); ecchymosis

INTEG:
Rash, pruritus

MISC:
Flulike symptoms

SYST:
Stevens-Johnson syndrome,
metabolic acidosis

PHARMACOKINETICS

Peak 2-6 hr, half-life in RBCs 105 hr, metabolized by liver, excreted by kidneys, protein binding 40%

INTERACTIONS

Decrease:
half-life of zonisamide—carBAMazepine, phenytoin, PHENobarbital

Altered product levels:
CYP3A4 inhibitors/inducers

Increase:
CNS depression—alcohol

Drug/Herb

Increase:
effect of this product—St. John’s wort

Drug/Food

• 
Do not use with grapefruit

Drug/Lab Test

Increase:
BUN, creatinine

NURSING CONSIDERATIONS
Assess:

• 
Seizures:
duration, type, intensity, precipitating factors

• 
Renal function: albumin conc, BUN, creatinine, serum bicarbonate at baseline and periodically

 
Mental status: mood, sensorium, affect, memory (long, short term),
suicidal thoughts/behaviors

• 
Stevens-Johnson syndrome, aplastic anemia, fulminant hepatic necrosis; may cause death; monitor for rashes and hypersensitive reactions

• 
Rash, hypersensitivity reactions

• 
Obtain bicarbonate before treatment/periodically; metabolic acidosis may occur in child

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 of rash immediately; to notify prescriber of back pain, abdominal pain, blood in urine; to increase fluid intake to reduce risk of kidney stones

• 
To notify prescriber if pregnancy planned, suspected

• 
To avoid grapefruit

• 
To notify prescriber of sore throat, fever, easy bruising

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

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