Darifenacin hydrobromide and Memory loss - a phase IV clinical study of FDA data

Summary:

Memory loss is reported as a side effect among people who take Darifenacin hydrobromide (darifenacin hydrobromide), especially for people who are female, 50-59 old, also take Lisinopril, and have Arthritis.

The phase IV clinical study analyzes which people have Memory loss when taking Darifenacin hydrobromide. It is created by eHealthMe based on reports of 511 people who have side effects when taking Darifenacin hydrobromide from the FDA, and is updated regularly.

What is Darifenacin hydrobromide?

Darifenacin hydrobromide has active ingredients of darifenacin hydrobromide. eHealthMe is studying from 512 Darifenacin hydrobromide users. Check the latest studies of Darifenacin hydrobromide.

What is Memory loss?

Memory loss is found to be associated with 2,726 drugs and 4,378 conditions by eHealthMe. Check the latest studies of Memory loss.

eHealthMe: drug outcomes in the real world

eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.

On Sep, 04, 2026

511 people reported to have side effects when taking Darifenacin hydrobromide.
Among them, 15 people (2.94%) have Memory loss.

Could Darifenacin hydrobromide cause Memory loss?

Among these 15 people:

What is the gender of people who have Memory loss when taking Darifenacin hydrobromide? *

female: 93.33 %
male: 6.67 %

What is the age of people who have Memory loss when taking Darifenacin hydrobromide? *

What are other drugs people take besides Darifenacin hydrobromide? *

What are other side effects people have besides Memory loss? *

Fatigue (feeling of tiredness): 13 people, 86.67%
Muscle Spasms (muscle contraction): 12 people, 80.00%
Stress And Anxiety: 12 people, 80.00%
Pain In Extremity: 12 people, 80.00%
Fall: 12 people, 80.00%
Drug Effect Decreased: 11 people, 73.33%
Malaise (a feeling of general discomfort or uneasiness): 11 people, 73.33%
Joint Pain: 11 people, 73.33%
Irritability: 11 people, 73.33%
Headache (pain in head): 11 people, 73.33%

What are the existing conditions these people have? *

Thyroid Diseases: 11 people, 73.33%
Quit Smoking: 11 people, 73.33%
Asthma: 11 people, 73.33%
Bladder Disorder: 11 people, 73.33%
Depression: 11 people, 73.33%
High Blood Cholesterol: 11 people, 73.33%
High Blood Pressure: 11 people, 73.33%
Neuralgia (pain in one or more nerves): 11 people, 73.33%
Pneumonia: 11 people, 73.33%
Arthritis (form of joint disorder that involves inflammation of one or more joints): 11 people, 73.33%

* Approximation only. Some reports may have incomplete information.

Do you take Darifenacin hydrobromide and have Memory loss?

- Check whether Memory loss 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 Darifenacin hydrobromide:

Darifenacin hydrobromide (512 reports)

Memory loss treatments and more:

Memory loss (244,445 reports)

Browse all side effects of Darifenacin hydrobromide:

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 Memory loss:

Memory loss (2,726 drugs)

Browse all the conditions that are associated with Memory loss:

Memory loss (4,378 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on darifenacin hydrobromide (the active ingredients of Darifenacin hydrobromide) and Darifenacin hydrobromide (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.