ZALEPLON
(zal′ep-lon)
Sonata
Classifications: ANXIOLYTIC;
SEDATIVE-HYPNOTIC;
NONBENZODIAZEPINE
Therapeutic: SEDATIVE-HYPNOTIC;
ANTIANXIETY
Prototype: Zolpidem
Pregnancy Category: C
Controlled Substance: Schedule IV
AVAILABILITY
Capsule
ACTION & THERAPEUTIC EFFECT
Short-acting nonbenzodiazepine
with sedative-hypnotic, muscle relaxant.
Reduces difficulty in initially
falling asleep. Preserves deep sleep
(stage 3 through stage 4) at hypnotic
dose with minimal-to-absent rebound
insomnia when discontinued.
USES
Short-term treatment of insomnia.
CONTRAINDICATIONS
Hypersensitivity
to zaleplon, or tartrazine dye
(Yellow 5); severe hepatic impairment;
suicidal ideation.
CAUTIOUS USE
Hypersensitivity
to salicylates; chronic depression;
history of suicidal thoughts; history
of drug abuse; COPD; respiratory
insufficiency; hepatic impairment;
pulmonary disease; older adults;
pregnancy (category C); lactation.
Safe use in children not established.
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NURSING IMPLICATIONS ZALEPLON Sonata |
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ROUTE & DOSAGE
Insomnia
Adult:
PO 10 mg at bedtime (max:
20 mg at bedtime)
Geriatric:
PO 5 mg at bedtime
(max: 10 mg at bedtime)
ADMINISTRATION
Oral
- Give immediately before bedtime;
not while patient is still ambulating.
- Ensure that extended release tablets
are swallowed whole and are
not crushed or chewed.
- Sublingual tablets should not be
given with water and should not
be swallowed
- Oral spray container must be
primed before first use. Ensure
that a full dose (5 mg) is sprayed
directly into the mouth over the
tongue. For a 10 mg dose, administer
a second spray.
- Store at 20°–25° C (68°–77° F).
ADVERSE EFFECTS (≥1%)
Body
as a Whole: Asthenia, fever, headache,
migraine, myalgia, back pain.
CNS: Amnesia, dizziness, paresthesia,
somnolence, tremor, vertigo,
depression, hypertonia, nervousness,
difficulty concentrating. GI:
Abdominal pain, dyspepsia, nausea,
constipation, dry mouth. Respiratory:
Bronchitis. Skin: Pruritus,
rash. Special Senses: Eye pain, hyperacusis,
conjunctivitis. Urogenital:
Dysmenorrhea.
INTERACTIONS
Drug: Alcohol,
imipramine, thioridazine may
cause additive CNS impairment; rifampin
increases metabolism of zaleplon;
cimetidine increases serum
levels of zaleplon. Herbal: Valerian,
melatonin may produce additive
sedative effects. Food: High-fat
meals may delay absorption.
PHARMACOKINETICS
Absorption:
Rapidly and completely absorbed,
30% reaches systemic circulation.
Onset: 15–20 min. Peak:
1 h. Duration: 3–4 h. Distribution:
60% protein bound. Metabolism:
Extensively in liver (CYP3A4) to inactive
metabolites. Elimination: 70%
in urine, 17% in feces. Half-Life: 1 h.
NURSING IMPLICATIONS
Assessment & Drug Effects
- Monitor behavior and notify prescriber
for significant changes.
Use extra caution with preexisting
clinical depression.
- Provide safe environment and
monitor ambulation after drug is
ingested.
- Monitor respiratory status with
preexisting compromised pulmonary
function.
Patient & Family Education
- Exercise caution when walking;
avoid all hazardous activities after
taking zaleplon.
- Do not take in combination with
alcohol or any other sleep medication.
- Note: Exhibits altered effectiveness
if taken with/immediately
after high-fat meal.
- Do not use longer than 2–3 wk.
- Expect possible mild/brief rebound
insomnia after discontinuing
regimen.
- Report use of OTC medications to
prescriber (e.g., cimetidine).
- Report pregnancy to prescriber
immediately.
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