NABILONE (nab'i-lone)
Cesamet Classifications: synthetic cannabinoid; antiemetic; Therapeutic:antiemetic; cannabinoid Pregnancy Category: C Controlled Substance: Schedule II
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Availability
1 mg capsules
Action
Nabilone is a synthetic cannabinoid with multiple effects on the CNS. It is thought that the antiemetic effect results from
its interaction with the cannabinoid receptor system (CB 1 receptor) in neural tissues. In therapeutic doses, it produces
relaxation, drowsiness, and euphoria.
Therapeutic Effect
It effectively controls emesis in patients receiving chemotherapy when other drugs have failed.
Uses
Prevention and treatment of nausea and vomiting in adult patients induced by cancer chemotherapy refractory to standard antiemetic
therapy.
Contraindications
Hypersensitivity to any cannabinoid; hypovolemia; pregnancy (category C); lactation.
Cautious Use
Children; older adults; history of psychosis.
Route & Dosage
Nausea and Vomiting Adult: PO Initial dose of 1 or 2 mg b.i.d. 13 h before chemotherapy. May increase to max of 2 mg t.i.d. May continue for 48 h
after last dose of chemotherapy.
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Administration
Oral
- Give 13 h before chemotherapy is begun. A dose of 12 mg the night before chemotherapy may be helpful in relieving
nausea.
- Store at 15°30° C (59°86° F).
Adverse Effects (≥1%)
CNS: Asthenia,
ataxia, confusion difficulties, depersonalization,
depression, disorientation,
drowsiness, dysphoria, euphoria, headache, sedation,
sleep disturbance, vertigo. CV: Hypotension.
GI: Anorexia,
dry mouth, increased appetite, nausea.
Special Senses: Visual disturbances.
Interactions
Drug: sedatives, hypnotics, and other psychoactive substances can potentiate the
CNS effects of nabilone. Coadministration of cannabinoids with
amphetamine, cocaine, tricyclic antidepressants, and/or
sympathomimetic agents can produce additive hypertension and tachycardia. Coadministration of cannabinoids with
antihistamines or
anticholinergic agents can produce additive tachycardia and drowsiness. Coadministration of cannabinoids with
barbiturates, benzodiazepines,
buspirone, ethanol, lithium, muscle relaxants,
opioids, and other
cns depressants can produce additive drowsiness and CNS-depressant effects.
Food: Alcohol can potentiate the
CNS effects of nabilone.
Pharmacokinetics
Absorption: Complete absorption from GI tract.
Peak: 2 h.
Metabolism: Extensive
hepatic metabolism.
Elimination: Fecal (major) and urine.
Half-Life: 2 h.
Nursing Implications
Assessment & Drug Effects
- Monitor for and report S&S of adverse psychiatric reactions (e.g., disorientation, hallucinations, psychosis) for 4872
h after last dose of nabilone.
- Monitor for S&S of tachycardia and postural hypotension, especially in the older adult and those with a history of heart
disease or hypertension.
- Lab tests: Periodic CBC with Hgb & Hct.
Patient & Family Education
- Do not use alcohol or other CNS depressants while using this medication.
- Do not drive or engage in potentially hazardous activities until response to drug is known.
- Report any of the following to a health care provider: confusion, disorientation, hallucinations, or other bizarre behavior.