Lucentis and Haematuria aggravated - a phase IV clinical study of FDA data

Summary:

Haematuria aggravated 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 1 - 6 months also take Aspirin, and have Age-related macular degeneration.

The phase IV clinical study analyzes which people have Haematuria aggravated 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 Haematuria aggravated?

Haematuria aggravated (presence of blood in urine) is found to be associated with 1,725 drugs and 1,767 conditions by eHealthMe. Check the latest studies of Haematuria aggravated.

On Jul, 17, 2026

25,577 people reported to have side effects when taking Lucentis.
Among them, 16 people (0.06%) have Haematuria aggravated.

Could Lucentis cause Haematuria aggravated?

Among these 16 people:

How long have people been on Lucentis when they have Haematuria aggravated? *

What is the gender of people who have Haematuria aggravated when taking Lucentis? *

female: 30.77 %
male: 69.23 %

What is the age of people who have Haematuria aggravated when taking Lucentis? *

What are other drugs people take besides Lucentis? *

Avastin: 3 people, 18.75%
Aspirin: 3 people, 18.75%
Acetaminophen: 2 people, 12.50%
Fish Oil: 2 people, 12.50%
Bimatoprost: 2 people, 12.50%
Zymar: 2 people, 12.50%
Axitinib: 1 person, 6.25%
Amiodarone Hydrochloride: 1 person, 6.25%
Carvedilol: 1 person, 6.25%
Coumadin: 1 person, 6.25%

What are other side effects people have besides Haematuria aggravated? *

Anaemia (lack of blood): 5 people, 31.25%
High Blood Pressure: 3 people, 18.75%
Oedema (fluid collection in tissue): 3 people, 18.75%
Hypokalemia (low potassium): 2 people, 12.50%
Renal Impairment (severely reduced kidney function): 2 people, 12.50%
Vitreous Haemorrhage (intraocular (inside the eye) bleeding): 2 people, 12.50%
Dry Eyes (lack of adequate tears): 2 people, 12.50%
Death: 2 people, 12.50%
Mood Swings (an extreme or rapid change in mood): 2 people, 12.50%
Cystoid Macular Oedema (fluid accumulation after cataract surgery): 2 people, 12.50%

What are the existing conditions these people have? *

Age-Related Macular Degeneration: 4 people, 25.00%
Renal Cell Carcinoma (a kidney cancer): 1 person, 6.25%
Diabetic Retinal Oedema (excessive build-up of fluid in the retina due to diabetes): 1 person, 6.25%
Choroidal Neovascularisation (creation of new blood vessels in vascular layer of eye): 1 person, 6.25%
Bladder Cancer: 1 person, 6.25%

* Approximation only. Some reports may have incomplete information.

Do you take Lucentis and have Haematuria aggravated?

- Check whether Haematuria aggravated 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 Haematuria aggravated:

Haematuria aggravated (1,725 drugs)

Browse all the conditions that are associated with Haematuria aggravated:

Haematuria aggravated (1,767 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.