Mosby's 2014 Nursing Drug Reference (146 page)

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

DULoxetine (Rx)

(du-lox′uh-teen)

Cymbalta

Func. class.:
Antidepressant

Chem. class.:
Serotonin-norepinephrine reuptake inhibitor (SNRI)

ACTION:

May potentiate serotonergic, noradrenergic activity in the CNS; in studies, DULoxetine is a potent inhibitor of neuronal serotonin and norepinephrine reuptake

USES:

Major depressive disorder (MDD), neuropathic pain associated with diabetic neuropathy, generalized anxiety disorder, fibromyalgia, chronic low back pain, osteoarthritis pain

Unlabeled uses:
Stress, urinary incontinence

CONTRAINDICATIONS:

Alcohol intoxication, alcoholism, closed-angle glaucoma, hepatic disease, hepatitis, jaundice, hypersensitivity

Precautions:
Pregnancy (C), breastfeeding, geriatric patients, mania, hypertension, renal/cardiac disease, seizures, increased intraocular pressure, anorexia nervosa, bleeding, dehydration, diabetes, hyponatremia, hypotension, hypovolemia, orthostatic hypotension, abrupt product withdrawal

 

Black Box Warning:

Children, suicidal ideation

DOSAGE AND ROUTES
Calculator
Depression


Adult: PO
40-60 mg/day as single dose or 2 divided doses

Diabetic neuropathy


Adult: PO
60 mg/day

Generalized anxiety disorder


Adult: PO
60 mg/day, may start with 30 mg/day × 1 wk then increase to 60 mg/day; maintenance 60-120 mg/day

Fibromyalgia


Adult: PO
30 mg/day × 1 wk then 60 mg/day

Musculoskeletal pain


Adult: PO
60 mg/day or 30 mg/day × 1 wk then 60 mg/day

Renal dose


 
Adult: PO
Start with 20 mg, gradually increase; avoid use in severe renal disease

Available forms:
Caps 20, 30, 60 mg

Administer:

• 
Swallow cap whole; do not break, crush, or chew; do not sprinkle on food or mix with liquid

• 
Without regard to food

SIDE EFFECTS

CNS:
Insomnia, anxiety, dizziness, tremor, somnolence, fatigue, decreased appetite, decreased weight, agitation, diaphoresis, hallucinations,
neuroleptic malignant–like syndrome reaction,
aggression,
seizures,
headache

CV:
Thrombophlebitis,
peripheral edema, hypertension, palpitations,
supraventricular dysrhythmia

EENT:
Abnormal vision

ENDO:
Hypo/hyperglycemia

GI:
Constipation, diarrhea, dysphagia,
nausea
, vomiting, anorexia, dry mouth, colitis, gastritis, abdominal pain,
hepatic failure

GU:
Abnormal ejaculation, urinary hesitation/retention/frequency, ejaculation delayed, erectile dysfunction, gynecologic bleeding

INTEG:
Photosensitivity, bruising, sweating,
Stevens-Johnson syndrome

MS:
Gait disturbance, muscle spasm, restless leg syndrome

SYST:
Anaphylaxis, angioedema, serotonin syndrome, Stevens-Johnson syndrome

PHARMACOKINETICS

Well absorbed; extensively metabolized (CYP2D6, CYP1A2) in the liver to an ac
tive metabolite; 70% of product recovered in urine, 20% in feces; 90% protein binding; elimination half-life 9.2-19.1 hr

INTERACTIONS


 
Do not use with linezolid or methylene blue IV


 
Narrow therapeutic index: CYP2D6 extensively metabolized products (flecainide, phenothiazines, propafenone, tricyclics, thioridazine)

 
Hyperthermia, rigidity, rapid fluctuations of vital signs, mental status changes, neuroleptic malignant syndrome—MAOIs, coadministration contraindicated within 14 days of MAOI use

Increase:
CNS depression—opioids, antihistamines, sedative/hypnotics

Increase:
serotonin syndrome, neuroleptic malignant syndrome—SSRIs, serotonin-receptor agonists

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

Increase:
action of DULoxetine—CYP1A2 inhibitors (fluvoxamine, quinolone antiinfectives); CYP2D6 inhibitors (FLUoxetine, quiNIDine, PARoxetine)

Increase:
ALT, bilirubin—alcohol

Drug/Herb

• 
Serotonin syndrome: St. John’s wort

Increase:
CNS depression—kava, valerian

Drug/Lab Test

Increase:
blood glucose

NURSING CONSIDERATIONS
Assess:

 

Black Box Warning:

Depression:
mood, sensorium, affect,
suicidal tendencies,
increase in psychiatric symptoms; depression, panic, monitor children q wk face to face during first 4 wk, or dosage change, then every other week for next 4 wk, then at 12 wk

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

• 
Hepatic studies: AST, ALT, bilirubin

• 
Weight weekly; weight loss or gain; appetite may increase; peripheral edema may occur

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

• 
Withdrawal symptoms:
headache, nausea, vomiting, muscle pain, weakness; not common unless product is discontinued abruptly

 
Malignant neuroleptic-like syndrome reaction

 
Serotonin syndrome:
nausea/vomiting, dizziness, facial flush, shivering, sweating

• 
Sexual dysfunction:
ejaculation dysfunction, erectile dysfunction, decreased libido, orgasm dysfunction

Perform/provide:

• 
Storage in tight container at room temp; do not freeze

• 
Assistance with ambulation during beginning therapy; drowsiness, dizziness occur

• 
Confirmation that PO medication swallowed

Evaluate:

• 
Therapeutic response: decreased depression

Teach patient/family:

• 
To report urinary retention; about signs and symptoms of bleeding (GI bleeding, nosebleed, ecchymoses, bruising)

• 
To use with caution when driving, performing other activities requiring alertness because of drowsiness, dizziness, blurred vision

• 
To avoid alcohol ingestion, MAOIs, other CNS depressants

• 
Not to discontinue medication quickly after long-term use; may cause nausea, headache, malaise; taper

 

Black Box Warning:

That clinical worsening and suicide risk may occur

• 
To wear sunscreen or large hat; photosensitivity may occur

• 
To notify prescriber if pregnancy planned or suspected, or if breastfeeding

• 
Improvement may occur in 4-8 wk or in up to 12 wk (geriatric patients)

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

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