• Basic Info
• Top Questions
• Clinical Info

Uses

Schizophrenia

Symptomatic management of schizophrenia.

Bipolar Disorder

Management of acute manic and mixed episodes associated with bipolar I disorder.

Dosage and Administration

Administration

Oral Administration

Administer orally once daily without regard to meals.

Dosage

Oral solution may be given at same dose on mg-per-mg basis as the 5-, 10-, 15-, or 20-mg tablet strengths of the drug up to a dose of 25 mg. However, if oral solution is used in patients receiving aripiprazole 30-mg tablets, use a dose of 25 mg of the oral solution.

Adults

Schizophrenia

Oral

Initial and target dosage is 10 or 15 mg once daily.

Dosages ranging from 10–30 mg daily were effective in clinical trials; dosages exceeding 10–15 mg daily did not result in greater efficacy.

Adjust dosage at intervals of not less than 2 weeks, the time needed to achieve steady-state concentrations.

In patients responding to aripiprazole therapy, continue the drug as long as clinically necessary and tolerated, but at lowest possible effective dosage; periodically reassess need for continued therapy.

Long-term efficacy of aripiprazole has not been established, and optimum duration of therapy currently is not known. However, aripiprazole has been used as maintenance therapy for up to 26 weeks in clinical trials, and maintenance therapy with antipsychotic agents is well established.

Bipolar Disorder

Acute Mania and Mixed Episodes

Oral

Initial dosage of 30 mg once daily as tablets was used in clinical trials.

Dosage was decreased to 15 mg once daily in clinical trials if initial 30-mg dosage was not well tolerated.

Safety of dosages >30 mg daily has not been established.

Long-term efficacy (i.e., >6 weeks) of aripiprazole has not been established, and optimum duration of therapy currently is not known. Periodically reevaluate the long-term risks and benefits of the drug for the individual patient.

Special Populations

Patients Receiving CYP3A4 or CYP2D6 Inhibitors

Reduce aripiprazole dosage to one-half the usual dosage in patients receiving concomitant therapy with inhibitors of CYP3A4 (e.g., ketoconazole) or CYP2D6 (e.g., fluoxetine, paroxetine, quinidine); increase aripiprazole dosage to the usual dosage after discontinuance of the CYP3A4 or CYP2D6 inhibitor.

Patients Receiving CYP3A4 Inducers

Increase aripiprazole dosage to 20–30 mg daily upon initiation of concomitant therapy with drugs that induce CYP3A4 (e.g., carbamazepine); additional dosage escalation should be based on clinical evaluation. Decrease aripiprazole dosage to 10–15 mg daily if the CYP3A4 inducer is discontinued.

Cautions

Contraindications

• Known hypersensitivity to aripiprazole or any ingredient in the formulation.

Warnings/Precautions

Warnings

Increased Mortality in Geriatric Patients with Dementia-related Psychosis

Possible increased risk of death with use of atypical antipsychotics in geriatric patients with dementia-related psychosis.

Increased incidence of adverse cerebrovascular effects (e.g., stroke, TIA), including fatalities, observed in geriatric patients (78–88 years of age) with dementia-related psychosis treated with aripiprazole in several placebo-controlled studies. A statistically significant dose-response relationship for adverse cerebrovascular effects was observed in patients receiving the drug in a fixed-dose study.

Safety and efficacy not established in patients with dementia-related psychosis; exercise caution if used. (See Boxed Warning and see Geriatric Use under Cautions.)

Neuroleptic Malignant Syndrome

Neuroleptic malignant syndrome (NMS), a potentially fatal syndrome requiring immediate discontinuance of the drug and intensive symptomatic treatment, has been reported.

Tardive Dyskinesia

Tardive dyskinesia, a syndrome of potentially irreversible, involuntary dyskinetic movements, has been reported. Consider discontinuance of aripiprazole.

Hyperglycemia and Diabetes Mellitus

Severe hyperglycemia, sometimes associated with ketoacidosis, hyperosmolar coma, or death, reported in patients receiving atypical antipsychotic agents. Although there have been few reports of hyperglycemia in patients receiving aripiprazole, it is not known whether the paucity of such reports is due to relatively limited experience with the drug.

Closely monitor patients with preexisting diabetes mellitus for worsening of glucose control and perform fasting glucose tests at baseline and periodically for patients with risk factors for diabetes (e.g., obesity, family history of diabetes). If manifestations of hyperglycemia occur, perform fasting blood glucose testing.

General Precautions

Cardiovascular Effects

Orthostatic hypotension reported. Use with caution in patients with known cardiovascular or cerebrovascular disease and/or conditions that would predispose patients to hypotension (e.g., dehydration, hypovolemia, concomitant antihypertensive therapy).

Nervous System Effects

Possible risk of seizures; use with caution in patients with a history of seizures or with conditions known to lower the seizure threshold (e.g., dementia of the Alzheimer’s type, geriatric patients).

Disruption of ability to reduce core body temperature possible; use caution in patients exposed to conditions that may contribute to an elevation in core body temperature (e.g., dehydration, extreme heat, strenuous exercise, concomitant use of anticholinergic agents).

Somnolence reported; most prominent in patients with schizophrenia receiving the aripiprazole 30-mg daily dosage during clinical trials. Potential impairment of judgment, thinking, or motor skills.

GI Effects

Esophageal dysmotility and aspiration possible; use with caution in patients at risk for aspiration pneumonia (e.g., geriatric patients, those with advanced Alzheimer’s dementia).

Suicide

Attendant risk with psychotic illnesses; closely supervise high-risk patients. Prescribe in the smallest quantity consistent with good patient management to reduce the risk of overdosage.

Metabolic Effects

Weight gain possible.

Specific Populations

Pregnancy

Category C.

Lactation

Distributed into milk in rats. Not known whether aripiprazole or its metabolites are distributed into milk in humans. Women receiving aripiprazole should not breast-feed.

Pediatric Use

Safety and efficacy not established in children <18 years of age.

Geriatric Use

Experience in those ≥65 years of age is insufficient to determine whether they respond differently from younger adults.

Tolerability profile may differ in patients ≥65 years of age with dementia-related psychosis, including psychosis in association with dementia of the Alzheimer’s type, compared with that in younger patients with schizophrenia. Possible increased risk of death. (See Boxed Warning and see Increased Mortality in Geriatric Patients with Dementia-related Psychosis under Cautions.)

Common Adverse Effects

In short-term studies, headache, agitation, anxiety, insomnia, nausea, dyspepsia, somnolence, akathisia, vomiting, constipation, lightheadedness, asthenia, extrapyramidal syndrome, accidental injury.

With longer-term (e.g., 26 weeks) use, adverse effects generally were consistent with those reported in short-term trials, except for a higher incidence of tremor.