Cabergoline PDF

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1 Adverse Reactions/Side Effects


CNS: dizziness, headache, depression, drowsiness, fatigue, nervousness, vertigo, PDF Page #1
cabergoline (ka-ber-goe-leen) weakness. Resp: PULMONARY FIBROSIS, pleural effusion. EENT: abnormal vision.
Dostinex CV: PERICARDIAL FIBROSIS, VALVULAR DISORDERS, postural hypotension, hot flashes.
Classification GI: RETROPERITONEAL FIBROSIS, constipation, nausea, abdominal pain, dyspepsia,
Therapeutic: antihyperprolactinemic vomiting. GU: dysmenorrhea. Endo: breast pain. Neuro: paresthesia.
Pharmacologic: dopamine agonists
Interactions
Pregnancy Category B Drug-Drug:qrisk of hypotension with antihypertensives. Mayqthe effects of
SSRIs and other serotonin agonists (induces serotonin syndrome). Effectiveness
Indications may bepby phenothiazines, butyrophenones (haloperidol), thioxanthenes,
Treatment of hyperprolactinemia (idiopathic or pituitary in origin). or metoclopramide (avoid concurrent use).
Action Route/Dosage
Inhibits secretion of prolactin by acting as a dopamine agonist. Therapeutic Ef- PO (Adults): 0.25 mg twice weekly; may beqat 4-wk intervals up to 1 mg twice
fects: Decreased secretion of prolactin in hyperprolactinemia. weekly.
Pharmacokinetics NURSING IMPLICATIONS
Absorption: Well absorbed but undergoes extensive first-pass hepatic metabo-
lism. Assessment
Distribution: Widely distributed; concentrates in pituitary. ● Monitor BP before and frequently during initial therapy. Initial doses ⬎1 m g may
Metabolism and Excretion: Extensively metabolized by the liver; ⬍4% excreted cause orthostatic hypotension. Use with caution when administering concurrently
unchanged in urine. with other medications that lower BP. Supervise ambulation and transfer during
Protein Binding: 40– 42%. initial dosing to prevent injury from hypotension.
Half-life: 63– 69 hr. ● Evaluate the cardiac status and monitor echocardiography at baseline
TIME/ACTION PROFILE (effect on serum prolactin levels) and every 6– 12 mo after initiation of therapy or as indicated clinically
ROUTE ONSET PEAK DURATION
by signs and symptoms of valvular disease (dyspnea, edema, HF, new
cardiac murmur). Use lowest dose and reassess need for therapy peri-
PO unknown 2–3 hr unknown
odically.
Contraindications/Precautions ● Monitor for signs and symptoms of pulmonary fibrosis (dyspnea, per-
Contraindicated in: Hypersensitivity to cabergoline or ergot alkaloids; Uncon- sistent coughing, difficulty with breathing while lying down, peripheral
trolled hypertension; History of pulmonary, pericardial, or retroperitoneal fibrotic edema) periodically during therapy. Obtain chest x-ray prior to therapy
disorders; History of cardiac valvular disease; Lactation: Has been associated with and chest x-ray and CT scan periodically during therapy to assess for
hypertension, stroke, and seizures. Not to be used for suppression of physiologic lac- pulmonary fibrosis.
tation. ● Lab Test Considerations: Monitor serum prolactin concentrations monthly
Use Cautiously in: Hepatic impairment; Patients who have received medications until normalized (⬍20 mcg/L in women and ⬍15 mcg/L in men).
associated with valvular disorders; OB: Use only if clearly needed; Pedi: Safety not ● Monitor erythrocyte sedimentation rate (ESR) and creatinine at baseline and as
established. needed during therapy.
⫽ Canadian drug name. ⫽ Genetic Implication. CAPITALS indicate life-threatening, underlines indicate most frequent. Strikethrough ⫽ Discontinued.
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2
Potential Nursing Diagnoses PDF Page #2
Risk for injury (Side Effects)
Impaired physical mobility (Indications)
Implementation
● PO: May be taken without regard to food.

Patient/Family Teaching
● Instruct patient to take medication as directed. Take missed doses as soon as pos-
sible within 1 or 2 days. If not remembered until time of next dose, double dose. If
nausea occurs, discuss with health care professional.
● May cause drowsiness and dizziness. Caution patient to avoid driving and other ac-
tivities requiring alertness until response to medication is known.
● Advise patient to change positions slowly to minimize orthostatic hypotension.
● Caution patient to avoid concurrent use of alcohol during therapy.
● Instruct patients taking cabergoline for pituitary tumors to inform health care pro-
fessional immediately if signs of tumor enlargement occur (blurred vision, sudden
headache, severe nausea, and vomiting).
● Advise patient to notify health care professional if signs of valvular disorders
(shortness of breath, swelling in extremities) occurs.
● Advise women to consult with health care professional regarding a nonhormonal
method of birth control. Women should contact health care professional promptly
if pregnancy is planned or suspected.
● Emphasize the importance of regular follow-up exams to determine effectiveness
and monitor side effects.
Evaluation/Desired Outcomes
● Decrease in galactorrhea in patients with hyperprolactinemia.
● After a normal serum prolactin level has been maintained for more than 6 mo, ca-
bergoline may be discontinued. Serum prolactin levels should be monitored peri-
odically to determine necessity of reinstituting cabergoline.
Why was this drug prescribed for your patient?

䉷 2015 F.A. Davis Company

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