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Proven safety for your adult patients1,2*

Adverse Reactions Injection Site Pain Prolactin & EPS Metabolic Data

ABILIFY ASIMTUFII® (aripiprazole) offers the established safety profile of
ABILIFY MAINTENA® (aripiprazole)1

Adverse reactions, ≥2% population (12-week study of ABILIFY MAINTENA vs placebo in adult patients living with schizophrenia)1

SYSTEM ORGAN CLASS PREFERRED TERM ABILIFY MAINTENA
(%, n=167) PLACEBO (%, n=172) GASTROINTESTINAL 
DISORDERS Constipation Dry mouth Diarrhea Vomiting Abdominal discomfort 10 4 3 3 2 7 2 2 1 1 GENERAL DISORDERS AND
ADMINISTRATION SITE CONCERNS Injection site pain 5 1 INFECTIONS AND
INFESTATIONS Upper respiratory
tract infection 4 2 INVESTIGATIONS Increased weight Decreased weight 17 4 7 2 MUSCULOSKELETAL
AND CONNECTIVE 
TISSUE DISORDERS Arthralgia Back pain Myalgia Musculoskeletal pain 4 4 4 3 1 2 2 1 NERVOUS SYSTEM
DISORDERS Akathisia Sedation Dizziness Tremor 11 5 4 3 4 1 2 1 RESPIRATORY, THORACIC 
AND MEDIASTINAL Nasal congestion 2 1
PREFERRED TERM ABILIFY MAINTENA
(%, n=167) PLACEBO
(%, n=172) GASTROINTESTINAL DISORDERS GASTROINTESTINAL DISORDERS Constipation 10 7 Dry mouth 4 2 Diarrhea 3 2 Vomiting 3 1 Abdominal discomfort 2 1 GENERAL DISORDERS AND ADMINISTRATION SITE CONCERNS GENERAL DISORDERS AND ADMINISTRATION SITE CONCERNS Injection 
site pain 5 1 INFECTIONS AND INFESTATIONS INFECTIONS AND INFESTATIONS Upper respiratory tract infection 4 2 INVESTIGATIONS INVESTIGATIONS Increased weight 17 7 Decreased weight 4 2 MUSCULOSKELETAL AND 
CONNECTIVE TISSUE DISORDERS MUSCULOSKELETAL AND 
CONNECTIVE TISSUE DISORDERS Arthralgia 4 1 Back pain 4 2 Myalgia 4 2 Musculoskel-etal pain 3 1 NERVOUS SYSTEM DISORDERS NERVOUS SYSTEM DISORDERS Akathisia 11 4 Sedation 5 1 Dizziness 4 2 Tremor 3 1 RESPIRATORY, THORACIC, 
AND MEDIASTINAL RESPIRATORY, THORACIC, 
AND MEDIASTINAL Nasal congestion 2 1 Most common adverse reactions (≥5% of patients and at least twice that for placebo), were increased weight, akathisia, injection site pain, and sedation.

Table excludes adverse reactions that had an incidence ≤ placebo.1

* Clinically stable on oral antipsychotic or ABILIFY MAINTENA.1,2

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ABILIFY ASIMTUFII works over a two-month time frame; this gives your patients the options of having fewer doses per year. — Gustavo Alva, MD, DFAPA

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Speakers are paid by Otsuka and Lundbeck and the opinions expressed are their own.

Injection site pain with ABILIFY ASIMTUFII and ABILIFY MAINTENA mainly occurred with the first injection and decreased in severity with further doses in both treatment groups5

32-week, open-label, multiple-dose, parallel-arm study: Mean intensity of injection site pain reported by patients receiving ABILIFY ASIMTUFII or ABILIFY MAINTENA5,6

The percentage of patients in the open-label study reporting any injection site-related adverse reactions (all reported as injection site pain) was 19% for patients treated with ABILIFY ASIMTUFII, and 9% for patients treated with ABILIFY MAINTENA.1

Mean pain intensity of injection site at 32 weeks, ABILIFY ASIMTUFII® and ABILIFY MAINTENA®, Graph
Mean pain intensity of injection site at 32 weeks, ABILIFY ASIMTUFII® and ABILIFY MAINTENA®, Graph

The following prolactin and EPS safety information is derived from 12-week, double-blind study in patients with schizophrenia2,3

* ABILIFY MAINTENA, n=99; placebo, n=66;2 † Incidence for ABILIFY MAINTENA vs placebo in female subjects (6.3% vs 13.8%) and male subjects (1.8% vs 10.8%).2

EPS=extrapyramidal symptoms; SD=standard deviation.

The following metabolic safety information was derived from a 12-week, placebo-controlled monotherapy study in patients with schizophrenia1

HDL=high-density lipoprotein; LDL=low-density lipoprotein.

The following metabolic safety information was derived from a 52-week, open-label study in patients with bipolar disorder initiated on ABILIFY MAINTENA.1

  • In those patients who initiated ABILIFY MAINTENA, 1.8% discontinued ABILIFY MAINTENA treatment due to weight increase1
  • ABILIFY MAINTENA was associated with mean increase in weight from baseline of 1.0 kg at Week 521
  • 21.4% of these patients demonstrated a ≥7% increase in body weight and 15.4% demonstrated a ≥7% decrease in body weight1

HDL=high-density lipoprotein; LDL=low-density lipoprotein.

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Dosing and initiation designed with your adult patients in mind.1,2

Explore Dosing and Administration
 

IMPORTANT SAFETY INFORMATION and INDICATIONS for ABILIFY ASIMTUFII® (aripiprazole) and ABILIFY MAINTENA® (aripiprazole)

WARNING: INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS

Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at increased risk of death (1.6 to 1.7 times) compared to placebo-treated patients. ABILIFY ASIMTUFII and ABILIFY MAINTENA are not approved for the treatment of patients with dementia-related psychosis.

Contraindication: Known hypersensitivity reaction to aripiprazole. Reactions have ranged from pruritus/urticaria to anaphylaxis.

Cerebrovascular Adverse Events, Including Stroke: Increased incidence of cerebrovascular adverse events (e.g., stroke, transient ischemic attack), including fatalities, have been reported in clinical trials of elderly patients with dementia-related psychosis treated with oral aripiprazole.

Neuroleptic Malignant Syndrome (NMS): NMS is a potentially fatal symptom complex reported in association with administration of antipsychotic drugs including aripiprazole. Clinical signs of NMS are hyperpyrexia, muscle rigidity, altered mental status and evidence of autonomic instability. Additional signs may include elevated creatine phosphokinase, myoglobinuria (rhabdomyolysis), and acute renal failure. Manage NMS with immediate discontinuation of aripiprazole, intensive symptomatic treatment, and monitoring.

Tardive Dyskinesia (TD): Risk of TD, and the potential to become irreversible, are believed to increase with duration of treatment and total cumulative dose of antipsychotic drugs. TD can develop after a relatively brief treatment period, even at low doses, or after discontinuation of treatment. Prescribing should be consistent with the need to minimize TD. If antipsychotic treatment is withdrawn, TD may remit, partially or completely.

Metabolic Changes: Atypical antipsychotic drugs have caused metabolic changes including:

  • Hyperglycemia/Diabetes Mellitus: Hyperglycemia, in some cases extreme and associated with ketoacidosis, hyperosmolar coma, or death, has been reported in patients treated with atypical antipsychotics including aripiprazole. Patients with diabetes mellitus should be regularly monitored for worsening of glucose control; those with risk factors for diabetes (e.g., obesity, family history of diabetes), should undergo baseline and periodic fasting blood glucose testing. Any patient treated with atypical antipsychotics should be monitored for symptoms of hyperglycemia including polydipsia, polyuria, polyphagia, and weakness. Patients who develop symptoms of hyperglycemia should also undergo fasting blood glucose testing. In some cases, hyperglycemia has resolved when the atypical antipsychotic was discontinued; however, some patients required continuation of antidiabetic treatment despite discontinuation of the suspect drug.
  • Dyslipidemia: Undesirable alterations in lipids have been observed in patients treated with atypical antipsychotics.
  • Weight Gain: Weight gain has been observed with atypical antipsychotic use. Clinical monitoring of weight is recommended.

Pathological Gambling and Other Compulsive Behaviors: Intense urges, particularly for gambling, and the inability to control these urges have been reported while taking aripiprazole. Other compulsive urges have been reported less frequently. Prescribers should ask patients or their caregivers about the development of new or intense compulsive urges. Consider dose reduction or stopping aripiprazole if such urges develop.

Orthostatic Hypotension or Syncope: ABILIFY ASIMTUFII and ABILIFY MAINTENA may cause orthostatic hypotension and should be used with caution in patients with known cardiovascular disease, cerebrovascular disease, or conditions which would predispose them to hypotension. Monitoring of orthostatic vital signs should be considered in patients who are vulnerable to hypotension.

Falls: Antipsychotics may cause somnolence, postural hypotension, motor and sensory instability, which may lead to falls causing fractures or other injuries. For patients with diseases, conditions, or medications that could exacerbate these effects, complete fall risk assessments when initiating treatment and recurrently during therapy.

Leukopenia, Neutropenia, and Agranulocytosis: Leukopenia, neutropenia, and agranulocytosis have been reported with antipsychotics. Monitor complete blood count in patients with pre-existing low white blood cell count (WBC)/absolute neutrophil count or history of drug-induced leukopenia/neutropenia. Discontinue ABILIFY ASIMTUFII or ABILIFY MAINTENA at the first sign of a clinically significant decline in WBC and in severely neutropenic patients.

Seizures: ABILIFY ASIMTUFII and ABILIFY MAINTENA should be used with caution in patients with a history of seizures or with conditions that lower the seizure threshold.

Potential for Cognitive and Motor Impairment: ABILIFY ASIMTUFII and ABILIFY MAINTENA may impair judgment, thinking, or motor skills. Patients should be cautioned about performing activities that require mental alertness such as operating hazardous machinery or operating a motor vehicle, until they are reasonably certain that therapy with ABILIFY ASIMTUFII or ABILIFY MAINTENA does not affect them adversely.

Body Temperature Regulation: Use ABILIFY ASIMTUFII or ABILIFY MAINTENA with caution in patients who may experience conditions that increase body temperature (e.g., strenuous exercise, extreme heat, dehydration, or concomitant use with anticholinergics).

Dysphagia: Esophageal dysmotility and aspiration have been associated with aripiprazole. Use caution in patients at risk for aspiration.

Alcohol: Advise patients to avoid alcohol while taking ABILIFY ASIMTUFII or ABILIFY MAINTENA.

Concomitant Medications: Dosage reductions are recommended in patients who are CYP2D6 poor metabolizers and/or in patients taking concomitant CYP3A4 inhibitors or CYP2D6 inhibitors for greater than 14 days. Avoid concomitant use of CYP3A4 inducers with ABILIFY ASIMTUFII and ABILIFY MAINTENA for greater than 14 days. Dosage adjustments are not recommended for patients with concomitant use of CYP3A4 inhibitors, CYP2D6 inhibitors or CYP3A4 inducers for less than 14 days.

Most Commonly Observed Adverse Reactions: The most commonly observed adverse reactions with ABILIFY MAINTENA in patients with schizophrenia (incidence of ≥5% and at least twice that for placebo) were increased weight, akathisia, injection site pain, and sedation.

Injection Site Reactions:

  • ABILIFY MAINTENA: In a short-term, clinical trial with ABILIFY MAINTENA in patients with schizophrenia treated with gluteally administered ABILIFY MAINTENA, the percent of patients reporting any injection site-related adverse reaction was 5.4% and 0.6% for placebo. In an open-label study of ABILIFY MAINTENA administered in the deltoid or gluteal muscle, injection site pain was observed at approximately equal rates.
  • ABILIFY ASIMTUFII: In an open-label study in patients with schizophrenia or bipolar I disorder, the percent of patients reporting any injection site-related adverse reactions was 19% for ABILIFY ASIMTUFII and 9.0% for ABILIFY MAINTENA. In both treatment groups, the majority of the injection site pain events coincided with the first injection and were reported with decreasing frequency upon subsequent injections. Patient-reported rating of pain was similar in both treatment groups at the last injection.

Dystonia: Symptoms of dystonia may occur in susceptible individuals during the first days of treatment and at low doses.

Pregnancy: Neonates exposed to antipsychotic drugs, including aripiprazole, during the third trimester of pregnancy are at risk for extrapyramidal and/or withdrawal symptoms. There are risks to the mother associated with untreated schizophrenia or bipolar I disorder and with exposure to antipsychotics, including ABILIFY ASIMTUFII and ABILIFY MAINTENA, during pregnancy.

Lactation: Aripiprazole is present in human breast milk. Monitor the breastfed infant for dehydration and lack of appropriate weight gain. The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for ABILIFY ASIMTUFII or ABILIFY MAINTENA and any potential adverse effects on the breastfed infant from ABILIFY ASIMTUFII or ABILIFY MAINTENA or from the underlying maternal condition.

To report SUSPECTED ADVERSE REACTIONS, contact Otsuka America Pharmaceutical, Inc. at 1‑800‑438-9927 or FDA at 1-800-FDA-1088 (www.fda.gov/medwatch).

INDICATIONS

ABILIFY ASIMTUFII® (aripiprazole) is an atypical antipsychotic indicated for treatment of schizophrenia in adults and maintenance monotherapy treatment of bipolar I disorder in adults.

ABILIFY MAINTENA® (aripiprazole) is an atypical antipsychotic indicated for treatment of schizophrenia in adults and maintenance monotherapy treatment of bipolar I disorder in adults.

Please see FULL PRESCRIBING INFORMATION, including BOXED WARNING, for ABILIFY ASIMTUFII and ABILIFY MAINTENA.

References: 1. ABILIFY ASIMTUFII® (aripiprazole) Prescribing Information. 2. ABILIFY MAINTENA® (aripiprazole) Prescribing Information. 3. Data on file. ABIMAI-124. 4. Kane JM, et al. Aripiprazole once-monthly in the acute treatment of schizophrenia: findings from a 12-week, randomized, double-blind, placebo-controlled study. J Clin Psychiatry. 2014;75(11):1254–1260. 5. Data on file. ABIASI-025. 6. Harlin M, et al. A randomized, open-label, multiple-dose, parallel-arm, pivotal study to evaluate the safety, tolerability, and pharmacokinetics of aripiprazole 2-month long-acting injectable in adults with schizophrenia or bipolar I disorder. CNS Drugs. 2023;37:337–350.