Ludiomil and Dizziness aggravated - a phase IV clinical study of FDA data

Summary:

Dizziness aggravated is reported as a side effect among people who take Ludiomil (maprotiline hydrochloride), especially for people who are female, 60+ old, have been taking the drug for < 1 month also take Lyrica, and have Depression.

The phase IV clinical study analyzes which people have Dizziness aggravated when taking Ludiomil. It is created by eHealthMe based on reports of 1,290 people who have side effects when taking Ludiomil from the FDA, and is updated regularly.

What is Ludiomil?

Ludiomil has active ingredients of maprotiline hydrochloride. eHealthMe is studying from 1,300 Ludiomil users. Check the latest studies of Ludiomil.

What is Dizziness aggravated?

Dizziness aggravated is found to be associated with 2,803 drugs and 974 conditions by eHealthMe. Check the latest studies of Dizziness aggravated.

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 Aug, 28, 2026

1,290 people reported to have side effects when taking Ludiomil.
Among them, 27 people (2.09%) have Dizziness aggravated.

Could Ludiomil cause Dizziness aggravated?

Among these 27 people:

How long have people been on Ludiomil when they have Dizziness aggravated? *

What is the gender of people who have Dizziness aggravated when taking Ludiomil? *

female: 66.67 %
male: 33.33 %

What is the age of people who have Dizziness aggravated when taking Ludiomil? *

What are other drugs people take besides Ludiomil? *

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

Dyspnea (difficult or laboured breathing): 7 people, 25.93%
Stress And Anxiety: 7 people, 25.93%
Malaise (a feeling of general discomfort or uneasiness): 6 people, 22.22%
Agitation (state of anxiety or nervous excitement): 6 people, 22.22%
Nausea And Vomiting: 6 people, 22.22%
Fall: 5 people, 18.52%
Sensation Of Pressure: 4 people, 14.81%
Fear: 4 people, 14.81%
Feeling Abnormal: 4 people, 14.81%
Hypoaesthesia (reduced sense of touch or sensation): 4 people, 14.81%

What are the existing conditions these people have? *

Depression: 16 people, 59.26%
Stress And Anxiety: 4 people, 14.81%
Trigeminal Neuralgia (a painful condition of the nerve responsible for most facial sensation): 3 people, 11.11%
Hypoaesthesia (reduced sense of touch or sensation): 3 people, 11.11%
Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development): 2 people, 7.41%
Insomnia (sleeplessness): 2 people, 7.41%
Ill-Defined Disorder: 2 people, 7.41%
High Blood Pressure: 2 people, 7.41%
Hallucination, Auditory (perceiving sounds without auditory stimulus): 1 person, 3.70%
Back Pain: 1 person, 3.70%

* Approximation only. Some reports may have incomplete information.

Do you take Ludiomil and have Dizziness aggravated?

- Check whether Dizziness aggravated is associated with a drug or a condition
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Related studies:

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

Ludiomil (1,300 reports)

Browse all side effects of Ludiomil:

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 Dizziness aggravated:

Dizziness aggravated (2,803 drugs)

Browse all the conditions that are associated with Dizziness aggravated:

Dizziness aggravated (974 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on maprotiline hydrochloride (the active ingredients of Ludiomil) and Ludiomil (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.