ZILEUTON
(zi-leu′ton)
Zyflo, Zyflo CR
Classifications: RESPIRATORY
SMOOTH MUSCLE RELAXANT;
BRONCHODILATOR; LEUKOTRIENE
RECEPTOR ANTAGONIST (LTRA)
Therapeutic: BRONCHODILATOR;
LTRA
Prototype: Zafirlukast
Pregnancy Category: C
AVAILABILITY
Immediate release
tablet; controlled release tablet
ACTION & THERAPEUTIC EFFECT
Inhibits 5-lipoxygenase, the enzyme
needed to start the conversion
of arachidonic acid to leukotrienes,
which are important
inflammatory agents that induce
bronchoconstriction and mucus production. Zileuton helps to prevent
the signs and symptoms of
asthma including airway edema,
smooth muscle constriction, and
altered cellular activity due to
inflammation.
USES
Prophylaxis and chronic
treatment of asthma in adults and
children older than 12 y.
CONTRAINDICATIONS
Hypersensitivity
to zileuton or zafirlukast,
active liver disease, status asthmaticus;
QT prolongation; lactation.
CAUTIOUS USE
Hepatic insufficiency;
alcoholism; fever; infection;
history of QT prolongation; older
females; older adults; pregnancy
(category C). Safety and effectiveness
in children younger than 12 y
are not established.
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NURSING IMPLICATIONS ZILEUTON / Zyflo CR |
Related for Nursing Implications and Drug Information
- Nuring Implications of ZIPRASIDONE HYDROCHLORIDE
- NURSING IMPLICATIONS ZIV-AFLIBERCEPT
- Nursing Implications of ZOLEDRONIC ACID (zo-le-dron′ic)
- Nursing Implications ZOLMITRIPTAN(zol-mi-trip′tan)
- Nursing Implications of ZOLPIDEM (zol′-pi-dem)
- Nursing Implications of ZONISAMIDE
ROUTE & DOSAGE
Asthma
Adult/Child (12 y or older):
PO
Controlled release:
1200 mg
b.i.d. OR
Immediate release:
600 mg q.i.d.
ADMINISTRATION
Oral
- Ensure that controlled release tablets
are swallowed whole. They
should not be crushed or chewed.
- Store at room temperature, 15°–
30° C (59°–86° F); protect from
light.
ADVERSE EFFECTS
(≥1%) Body as
a Whole: Pain, asthenia, myalgia,
arthralgia, fever, malaise, neck pain/
rigidity. CNS: Headache, dizziness,
insomnia, nervousness,
somnolence. CV: Chest pain. GI:
Abdominal pain, dyspepsia, nausea,
constipation, flatulence, vomiting,
elevated liver function tests,
asymptomatic hepatitis. Skin: Pruritus.
Other: Conjunctivitis, hypertonia,
lymphadenopathy, vaginitis,
UTI, leukopenia.
INTERACTIONS
Drug: May
double theophylline levels and
increase toxicity. Increases hypoprothrombinemic
effects of
warfarin. May increase levels of
BETA-BLOCKERS (especially propranolol),
leading to hypotension and
bradycardia.
PHARMACOKINETICS
Absorption:
Rapidly from GI tract. Peak:
1.7 h. Duration: 5–8 h. Distribution:
93% protein bound; secreted in the
breast milk of rats. Metabolism: In
liver primarily via glucuronide conjugation.
Elimination: Primarily in
urine (94%). Half-Life: 2.5 h.
NURSING IMPLICATIONS
Assessment & Drug Effects
- Assess respiratory status and airway
function regularly.
- Monitor closely each of the following
with concurrent drug
therapy: With theophylline,
theophylline levels; with warfarin,
PT and INR; with phenytoin,
phenytoin level; with propranolol,
HR and BP for excessive beta
blockade.
- Montior lab tests: Periodic CBC and
routine blood chemistry; monthly
LFTs for 3 mo, then every 2–3 mo
for rest of first year, then periodically.
Patient & Family Education
- Take medication regularly even
during symptom-free periods.
- Drug is not intended to treat acute
episodes of asthma.
- Report to prescriber promptly S&S
of hepatic toxicity (see Appendix F)
or flu-like symptoms. Follow-up
lab work is very important.
- Notify prescriber if condition
worsens while using prescribed
doses of all antiasthmatic medications
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