Mosby's 2014 Nursing Drug Reference (383 page)

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

telmisartan (Rx)

(tel-mih-sar′tan)

Micardis

Func. class.:
Antihypertensive

Chem. class.:
Angiotensin II receptor (Type AT
1
) antagonist

ACTION:

Blocks the vasoconstricting and aldosterone-secreting effects of angiotensin II; selectively blocks the binding of angiotensin II to the AT
1
receptor found in tissues

USES:

Hypertension, alone or in combination; stroke, MI prophylaxis (>55 yr) in patients unable to take ACE inhibitors

Unlabeled uses:
Heart failure

CONTRAINDICATIONS:

Hypersensitivity

 

Black Box Warning:

Pregnancy (D) 2nd/3rd trimesters

Precautions:
Pregnancy (C) 1st trimester, breastfeeding, children, geriatric patients; hypersensitivity to ACE inhibitors; renal/hepatic disease, renal artery stenosis, dialysis, CHF, hyperkalemia, hypotension, hypovolemia

DOSAGE AND ROUTES
Calculator

• Adult:
PO
40 mg/day; range 20-80 mg/day

Stroke, MI prophylaxis

• Adult >55 yr:
PO
80 mg/day

Available forms:
Tabs 20, 40, 80 mg

Administer:

• 
Without regard to meals

• 
Increased dose to African American patients or consider alternative agent; B/P response may be reduced

SIDE EFFECTS

CNS:
Dizziness, insomnia,
anxiety
, headache, fatigue

GI:
Diarrhea, dyspepsia,
anorexia, vomiting

MS:
Myalgia, pain

RESP:
Cough,
upper respiratory infection
, sinusitis, pharyngitis

PHARMACOKINETICS

Onset of antihypertensive activity 3 hr, peak 0.5-1 hr, extensively metabolized, terminal half-life 24 hr, protein binding 99.5%, excreted in feces >97%, B/P response is less in African American patients

INTERACTIONS

Increase:
digoxin peak/trough concentrations—digoxin

Increase:
antihypertensive action—diuretics, other antihypertensives, NSAIDs

Increase:
hyperkalemia—potassium-sparing diuretics, potassium salt substitutes

Decrease:
antihypertensive effect—NSAIDs, salicylates

Drug/Lab Test

Increase:
LFTs

NURSING CONSIDERATIONS
Assess:

• 
B/P, pulse standing, lying; note rate, rhythm, quality; if severe hypotension occurs, place in supine position and give IV NS

• 
Baselines of renal, hepatic studies before therapy begins

• 
CHF:
edema in feet, legs daily; jugular venous distention; dyspnea, crackles

Evaluate:

• 
Therapeutic response: decreased B/P

Teach patient/family:

• 
To comply with dosage schedule, even if feeling better; to take at same time of day; that therapeutic effect may take 2-4 wk

• 
To notify prescriber of mouth sores, fever, swelling of hands or feet, irregular heartbeat, chest pain, decreased urine output

• 
That excessive perspiration, dehydration, vomiting, diarrhea may lead to fall in blood pressure; to consult prescriber if these occur

• 
That product may cause dizziness, fainting, lightheadedness

 

Black Box Warning:

To notify prescriber if pregnancy is planned or suspected, pregnancy category (D) 2nd/3rd trimester

• 
To notify prescriber of all prescriptions, OTC products, and supplements taken

• 
Overdose:
dizziness, bradycardia or tachycardia

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

temazepam (Rx)

(te-maz′e-pam)

Restoril

Func. class.:
Sedative/hypnotic

Chem. class.:
Benzodiazepine, short to intermediate acting

 

Controlled Substance Schedule IV (USA), Schedule F (Canada)

Do not confuse:
temazepam
/flurazepam

ACTION:

Produces CNS depression at limbic, thalamic, hypothalamic levels of the 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 (generally 7-10 days)

CONTRAINDICATIONS:

Pregnancy (X), breastfeeding, hypersensitivity to benzodiazepines, intermittent porphyria

Precautions:
Children <15 yr, geriatric patients, anemia, renal/hepatic disease, suicidal individuals, drug abuse, psychosis, acute closed-angle glaucoma, seizure disorders, angioedema, sleep-related behaviors (sleepwalking), pulmonary disease

DOSAGE AND ROUTES
Calculator

• Adult:
PO
7.5 to 30 mg at bedtime

• Geriatric:
PO
7.5 mg at bedtime

Available forms:
Caps 7.5, 15, 22.5, 30 mg

Administer:

• 
1/2-1 hr before bedtime for sleeplessness

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

• 
Avoid use with CNS depressants; serious CNS depression may result

SIDE EFFECTS

CNS:
Lethargy, drowsiness, daytime sedation
, dizziness, confusion, light-headedness, headache, anxiety, irritability, complex sleep-related reactions (sleep driving, sleep eating), fatigue

CV:
Chest pain, pulse changes, hypotension

EENT:
Blurred vision

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

SYST:
Severe allergic reactions

PHARMACOKINETICS

Onset 30 min, peak 1-2 hr, duration 6-8 hr, half-life 10-20 hr, metabolized by liver, excreted by kidneys, crosses placenta, excreted in breast milk, 98% protein binding

INTERACTIONS

Increase:
effects of cimetidine, disulfiram, oral contraceptives

Increase:
action of both products—alcohol, CNS depressants

Increase:
effect of temazepam—probenecid

Decrease:
effect of antacids, theophylline, rifampin

Drug/Herb

Increase:
CNS depression—hops, kava, valerian, chamomile, skullcap

Drug/Food

Decrease:
temazepam effect—caffeine

Drug/Lab Test

Increase:
ALT, AST

NURSING CONSIDERATIONS
Assess:

• 
Mental status: mood, sensorium, affect, memory (long, short), orientation

• 
Type of sleep problem: falling asleep, staying asleep, baseline, periodically

• 
Dependency:
restrict amount given to patient, assess for physical/psychological dependency; high-level risk for abuse

Perform/provide:

• 
Assistance with ambulation after receiving dose

• 
Storage in tight container in cool environment

Evaluate:

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

Teach patient/family:

• 
To avoid driving, other activities requiring alertness until stabilized

• 
To avoid alcohol ingestion, other CNS depressants

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

• 
To limit to 7-10 days of continuous use

• 
About alternative measures to improve sleep: reading, exercise several hours before bedtime, warm bath, warm milk, TV, self-hypnosis, deep breathing

• 
Not to discontinue abruptly, withdraw gradually

• 
That complex sleep-related behaviors may occur: sleep driving/eating

• 
That hangover, memory impairment are common in geriatric patients but less common than with barbiturates

 
To notify prescriber if pregnancy is planned or suspected, pregnancy (X); to use contraception while taking this product

TREATMENT OF OVERDOSE:

Lavage, activated charcoal; monitor electrolytes, VS

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