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The company also marketed the drug to elderly patients, even though taking Abilify can be fatal for elderly patients with dementia. Other allegations claimed that Bristol-Myers Squibb marketed the drug to children, when the FDA had not approved it for treating children.

Anxiety Attention Deficit Hyperactivity Disorder Dementia Depression Insomnia Eating Disorders Obsessive-Compulsive Disorder Personality Disorder Post-Traumatic Stress Disorder Substance Abuse.

Being able to track ingestion of medications prescribed for mental illness may be useful for some patients, said Dr. Mitchell Mathis, director of the Division of Psychiatry Products in the FDA’s Center for Drug Evaluation and Research. The FDA . supports the development and use of new technology in prescription drugs and is committed to working with companies to understand how technology might benefit patients and prescribers.

Post-Marketing Surveillance Study of Aripiprazole in Patients With Autism; Assessment of Adverse Events in a Naive Pediatric Population Treated With an Antipsychotic; and Antipsychotic Induced Structural and Functional Brain Changes.

There are many ways that drugs and pharmaceuticals may be defective. This could include a design defect where the drug is not safe for the intended use or the drug manufacturer failed to properly warn the patientabout dangers involved with taking the drug.

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abilify is a brand name for the drug aripiprazole.