Abilify and Visual field defect - a phase IV clinical study of FDA data

Summary:

Visual field defect is reported as a side effect among people who take Abilify (aripiprazole), especially for people who are female, 40-49 old, have been taking the drug for 5 - 10 years also take Lamictal, and have Psychotic disorder.

The phase IV clinical study analyzes which people have Visual field defect when taking Abilify. It is created by eHealthMe based on reports of 97,308 people who have side effects when taking Abilify from the FDA, and is updated regularly.

What is Abilify?

Abilify has active ingredients of aripiprazole. It is often used in depression. eHealthMe is studying from 101,443 Abilify users. Check the latest studies of Abilify.

What is Visual field defect?

Visual field defect is found to be associated with 802 drugs and 1,024 conditions by eHealthMe. Check the latest studies of Visual field defect.

On Nov, 09, 2025

97,308 people reported to have side effects when taking Abilify.
Among them, 43 people (0.04%) have Visual field defect.

Could Abilify cause Visual field defect?

Among these 43 people:

How long have people been on Abilify when they have Visual field defect? *

What is the gender of people who have Visual field defect when taking Abilify? *

female: 69.77 %
male: 30.23 %

What is the age of people who have Visual field defect when taking Abilify? *

What are other drugs people take besides Abilify? *

What are other side effects people have besides Visual field defect? *

Dizziness: 12 people, 27.91%
Vision Blurred: 10 people, 23.26%
Weight Increased: 9 people, 20.93%
Hypotension (abnormally low blood pressure): 8 people, 18.60%
Tremor (trembling or shaking movements in one or more parts of your body): 7 people, 16.28%
Speech Impairment (Adult) (inability to speak (adult)): 7 people, 16.28%
High Blood Pressure: 6 people, 13.95%
Fatigue (feeling of tiredness): 6 people, 13.95%
Visual Impairment: 5 people, 11.63%
Memory Loss: 5 people, 11.63%

What are the existing conditions these people have? *

Psychotic Disorder: 7 people, 16.28%
Stress And Anxiety: 5 people, 11.63%
Attention Deficit Hyperactivity Disorder (a chronic condition including attention difficulty, hyperactivity, and impulsiveness): 4 people, 9.30%
Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development): 4 people, 9.30%
Insomnia (sleeplessness): 4 people, 9.30%
High Blood Pressure: 3 people, 6.98%
Intraocular Pressure Decreased: 3 people, 6.98%
Pain: 3 people, 6.98%
Multiple Sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath): 3 people, 6.98%
Diabetes: 2 people, 4.65%

* Approximation only. Some reports may have incomplete information.

Do you take Abilify and have Visual field defect?

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Related studies:

Effectiveness of, long term effects of, and alternative drugs to Abilify:

Abilify (101,443 reports)

Browse all side effects of Abilify:

a b c d e f g h i j k l m n o p q r s t u v w x y z

Browse all the drugs that are associated with Visual field defect:

Visual field defect (802 drugs)

Browse all the conditions that are associated with Visual field defect:

Visual field defect (1,024 conditions)

Drugs similar to Abilify and Visual field defect :

Related publications that referenced our studies

Cetin, M., Celik, M., Cakici, M., Polat, M., & Suner, A, "Aripiprazole-Induced Hoarseness", Turk Psikiyatri Dergisi, 2018 Jan .
Cetin M, Celik M, Cakici M, Polat M, Suner A, "Aripiprazole induced non-cardiogenic pulmonary edema: a case report", Turk Psikiyatri Dergisi, 2014 Dec .
Cetin, M., Celik, M., Cakici, M., Polat, M., & Suner, A, "Aripiprazole-Induced Hoarseness", Turk Psikiyatri Dergisi, 2018 Jan .
Cetin M, Celik M, Cakici M, Polat M, Suner A, "Aripiprazole induced non-cardiogenic pulmonary edema: a case report", Turk Psikiyatri Dergisi, 2014 Dec .

How the study uses the data?

The study uses data from the FDA. It is based on aripiprazole (the active ingredients of Abilify) and Abilify (the brand name). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Dosage of drugs is not considered in the study.

How to use the study?

DO NOT STOP MEDICATIONS without first consulting your doctor. If there are any serious or long term adverse effects discovered in the study, discuss the study with your doctor to ensure that proper medication management will be in place if applicable.

Who is eHealthMe?

With medical big data and proven AI/ML algorithms, eHealthMe provides a platform for everyone to run phase IV clinical trials. We study millions of patients and 5,000 more each day. Results of our real-world drug study have been referenced on 800+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and Nature. Our analysis results are available to researchers, health care professionals, patients (testimonials), and software developers (open API).

WARNING, DISCLAIMER, USE FOR PUBLICATION

WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.

DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only. Our phase IV clinical studies alone cannot establish cause-effect relationship. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.