Mosby's 2014 Nursing Drug Reference (97 page)

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

citalopram (Rx)

(sigh-tal′oh-pram)

Celexa

Func. class.:
Antidepressant

Chem. class.:
Selective serotonin reuptake inhibitor (SSRI)

Do not confuse:
CeleXA
/CeleBREX/Cerebyx/Cerebra/Zyprexa

ACTION:

Inhibits CNS neuron uptake of serotonin but not of norepinephrine; weak inhibitor of CYP450 enzyme system, thus making it more appealing than other products

USES:

Major depressive disorder

Unlabeled uses:
Premenstrual disorders, panic disorder, social phobia, impulsive aggression in children, obsessive-compulsive disorder in adolescents; treatment of psychotic symptoms in nondepressed demented patients; anxiety, hot flashes, menopause; adjunct in schizophrenia, PTSD

CONTRAINDICATIONS:

Hypersensitivity

Precautions:
Pregnancy (C), breastfeeding, geriatric patients, renal/hepatic disease, seizure disorder, hypersensitivity to escitalopram

 

Black Box Warning:

Children, suicidal ideation

DOSAGE AND ROUTES
Calculator
Depression

• Adult:
PO
20 mg/day
AM
or
PM
, may increase if needed to 40 mg/day after 1 wk; maintenance: after 6-8 wk of initial treatment, continue for 24 wk (32 wk total), reevaluate long-term usefulness (max 40 mg/day)

Hepatic dose/geriatric

• Adult:
PO
20 mg/day

Panic disorder (unlabeled)

• Adult:
PO
20-40 mg/day

Premenstrual dysphoria/social phobia (unlabeled)

• Adult:
PO
10-30 mg/day, used intermittently in premenstrual dysphoria

Available forms:
Tabs 10, 20, 40 mg; oral sol 10 mg/5 ml

Administer:

• 
With food or milk for GI symptoms

• 
Crushed if patient is unable to swallow medication whole

• 
Dosages at bedtime if oversedation occurs during the day; may take entire dose at bedtime

• 
Do not give within 14 days of MAOIs

SIDE EFFECTS

CNS:
Headache, nervousness, insomnia, drowsiness, anxiety, tremor, dizziness, fatigue, sedation, poor concentration, abnormal dreams, agitation
,
seizures,
apathy, euphoria, hallucinations, delusions, psychosis,
suicidal attempts, neuroleptic malignant-like syndrome reactions

CV:
Hot flashes, palpitations
, angina pectoris,
hemorrhage,
hypertension, tachycardia, 1st-degree AV block, bradycardia,
MI,
thrombophlebitis

EENT:
Visual changes, ear/eye pain, photophobia, tinnitus

GI:
Nausea, diarrhea, dry mouth, anorexia, dyspepsia, constipation, cramps, vomiting, taste changes, flatulence, decreased appetite

GU:
Dysmenorrhea, decreased libido, urinary frequency, UTI
, amenorrhea, cystitis, impotence, urine retention

INTEG:
Sweating, rash, pruritus
, acne, alopecia, urticaria

MS:
Pain
, arthritis, twitching

RESP:
Infection, pharyngitis, nasal congestion, sinus headache, sinusitis, cough, dyspnea, bronchitis
, asthma, hyperventilation, pneumonia

SYST:
Asthenia, viral infection, fever, allergy, chills;
hyponatremia (geriatric patients),
serotonin syndrome

PHARMACOKINETICS

Metabolized in liver by CYP3A4, CYP2C19; excreted in urine; steady state 1 wk; peak 4 hr; half-life 35 hr

INTERACTIONS

 
Fatal reactions: do not use with MAOIs

 
Increase:
QTc interval—dofetilide, halofantrine, probucol, pimoside, quinolones, ziprasidone; do not use together

Increase:
effect of tricyclics; use cautiously

Increase:
serotonin syndrome—serotonin receptor agonists, SSRIs, traMADol, lithium, MAOIs, traZODone, SNRIs (venlafaxine, DULoxetine)

Increase:
bleeding risk—NSAIDs, salicylates, thrombolytics, anticoagulants, antiplatelets

Increase:
CNS effects—barbiturates, sedative/hypnotics, other CNS depressants

Increase:
citalopram levels—macrolides, azole antifungals

Increase:
plasma levels of β-blockers

Decrease:
citalopram levels—carBAMazepine, cloNIDine

Drug/Herb

 
Increase:
serotonin syndrome—St. John’s wort, SAM-e; fatal reaction may occur; do not use concurrently

Increase:
CNS stimulation—yohimbe

Drug/Lab Test

Increase:
serum bilirubin, blood glucose, alk phos

Decrease:
VMA, 5-HIAA

False increase:
urinary catecholamines

NURSING CONSIDERATIONS
Assess:

 

Black Box Warning

Mental status: mood, sensorium, affect, suicidal tendencies, increase in psychiatric symptoms, depression, panic

 
Serotonin syndrome: increased heart rate, sweating, dilated pupils, tremors, twitching, hyperthermia, agitation

• 
B/P lying, standing, pulse q4hr; if systolic B/P drops 20 mm Hg, hold product, notify prescriber; take vital signs q4hr in patients with CV disease

• 
Weight weekly; appetite may decrease or increase with product

• 
Torsades de pointes, QT prolongation:
is dose-dependent, ECG for flattening of T wave, bundle branch, AV block, dysrhythmias in cardiac patients

• 
Alcohol consumption; if alcohol is consumed, hold dose until
AM

• 
Sexual dysfunction: erectile dysfunction, decreased libido

Perform/provide:

• 
Storage at room temp; do not freeze

• 
Assistance with ambulation during therapy, since drowsiness, dizziness occur

• 
Safety measures, primarily for geriatric patients

• 
Check to confirm PO medication swallowed

• 
Sugarless gum, hard candy, frequent sips of water for dry mouth

Evaluate:

• 
Therapeutic response: decreased depression

Teach patient/family:

• 
That therapeutic effect may take 4-6 wk, that patient may have increased anxiety 1st 5-7 days of therapy

• 
To use caution when driving, performing other activities that require alertness because of drowsiness, dizziness, blurred vision; to report signs, symptoms of bleeding

• 
To avoid alcohol, other CNS depressants

 

Black Box Warning:

That suicidal ideas, behavior may occur in children or young adults

• 
To notify prescriber if pregnant, planning to become pregnant, or breastfeeding

 
About the effects of serotonin syndrome: nausea/vomiting, tremors; if symptoms occur, to discontinue immediately, notify prescriber

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