Lucentis and Coordination abnormal - a phase IV clinical study of FDA data

Summary:

Coordination abnormal is reported as a side effect among people who take Lucentis (ranibizumab), especially for people who are male, 60+ old, have been taking the drug for 2 - 5 years also take Nexium, and have Age-related macular degeneration.

The phase IV clinical study analyzes which people have Coordination abnormal when taking Lucentis. It is created by eHealthMe based on reports of 25,577 people who have side effects when taking Lucentis from the FDA, and is updated regularly.

What is Lucentis?

Lucentis has active ingredients of ranibizumab. It is often used in macular degeneration. eHealthMe is studying from 25,647 Lucentis users. Check the latest studies of Lucentis.

What is Coordination abnormal?

Coordination abnormal (abnormal movement) is found to be associated with 983 drugs and 1,216 conditions by eHealthMe. Check the latest studies of Coordination abnormal.

On Jun, 25, 2026

25,577 people reported to have side effects when taking Lucentis.
Among them, 7 people (0.03%) have Coordination abnormal.

Could Lucentis cause Coordination abnormal?

Among these 7 people:

How long have people been on Lucentis when they have Coordination abnormal? *

What is the gender of people who have Coordination abnormal when taking Lucentis? *

female: 33.33 %
male: 66.67 %

What is the age of people who have Coordination abnormal when taking Lucentis? *

What are other drugs people take besides Lucentis? *

What are other side effects people have besides Coordination abnormal? *

Weakness: 5 people, 71.43%
Depression: 4 people, 57.14%
Macular Oedema (fluid and protein deposits collect on or under the macula of the eye (a yellow central area of the retina) and causes it to thicken): 3 people, 42.86%
Headache (pain in head): 3 people, 42.86%
Stress And Anxiety: 2 people, 28.57%
Memory Loss: 2 people, 28.57%
Malaise (a feeling of general discomfort or uneasiness): 2 people, 28.57%
Retinal Scar (development of scar tissue on retina): 2 people, 28.57%
Movement Disorder (neurological syndromes where they may be excess of movement or a paucity of movement that is not connected to weakness): 2 people, 28.57%
Stroke (sudden death of a portion of the brain cells due to a lack of oxygen): 2 people, 28.57%

What are the existing conditions these people have? *

Age-Related Macular Degeneration: 2 people, 28.57%
Lyme Disease (a bacterial infection that is spread to humans by infected ticks): 1 person, 14.29%
Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 1 person, 14.29%
Epilepsy (common and diverse set of chronic neurological disorders characterized by seizures): 1 person, 14.29%
Carcinoid Tumor: 1 person, 14.29%
Attention Deficit Hyperactivity Disorder (a chronic condition including attention difficulty, hyperactivity, and impulsiveness): 1 person, 14.29%

* Approximation only. Some reports may have incomplete information.

Do you take Lucentis and have Coordination abnormal?

- Check whether Coordination abnormal is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously

Related studies:

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

Lucentis (25,647 reports)

Browse all side effects of Lucentis:

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 Coordination abnormal:

Coordination abnormal (983 drugs)

Browse all the conditions that are associated with Coordination abnormal:

Coordination abnormal (1,216 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on ranibizumab (the active ingredients of Lucentis) and Lucentis (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.