Lactulose and Viith nerve paralysis - a phase IV clinical study of FDA data

Summary:

Viith nerve paralysis is reported as a side effect among people who take Lactulose (lactulose), especially for people who are female, 60+ old, have been taking the drug for 1 - 6 months also take Lantus, and have Diabetes.

The phase IV clinical study analyzes which people have Viith nerve paralysis when taking Lactulose. It is created by eHealthMe based on reports of 46,694 people who have side effects when taking Lactulose from the FDA, and is updated regularly.

What is Lactulose?

Lactulose has active ingredients of lactulose. It is often used in constipation. eHealthMe is studying from 46,960 Lactulose users. Check the latest studies of Lactulose.

What is Viith nerve paralysis?

Viith nerve paralysis is found to be associated with 521 drugs and 837 conditions by eHealthMe. Check the latest studies of Viith nerve paralysis.

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, 24, 2026

46,694 people reported to have side effects when taking Lactulose.
Among them, 11 people (0.02%) have Viith nerve paralysis.

Could Lactulose cause Viith nerve paralysis?

Among these 11 people:

How long have people been on Lactulose when they have Viith nerve paralysis? *

What is the gender of people who have Viith nerve paralysis when taking Lactulose? *

female: 54.55 %
male: 45.45 %

What is the age of people who have Viith nerve paralysis when taking Lactulose? *

What are other drugs people take besides Lactulose? *

What are other side effects people have besides Viith nerve paralysis? *

Weakness: 7 people, 63.64%
Speech Impairment (Adult) (inability to speak (adult)): 7 people, 63.64%
Fatigue (feeling of tiredness): 5 people, 45.45%
Hemiparesis (weakness on one side of the body): 5 people, 45.45%
Dizziness: 5 people, 45.45%
Dyspnea (difficult or laboured breathing): 4 people, 36.36%
Movement - Uncoordinated: 4 people, 36.36%
Pneumonia: 4 people, 36.36%
Metabolic Acidosis (body produces too much acid, or when the kidneys are not removing enough acid from the body): 4 people, 36.36%
Memory Loss: 4 people, 36.36%

What are the existing conditions these people have? *

Diabetes: 4 people, 36.36%
Multiple Myeloma (cancer of the plasma cells): 3 people, 27.27%
Lipids Increased (excess lipid in body): 3 people, 27.27%
Flatulence (flatus expelled through the anus): 3 people, 27.27%
Chronic Renal Failure (kidney failure): 3 people, 27.27%
Skin Disorder (skin disease): 1 person, 9.09%
Pain: 1 person, 9.09%
Osteoporosis (bones weak and more likely to break): 1 person, 9.09%
Knee Deformity (functional disability of knee): 1 person, 9.09%
Itching: 1 person, 9.09%

* Approximation only. Some reports may have incomplete information.

Do you take Lactulose and have Viith nerve paralysis?

- Check whether Viith nerve paralysis 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 Lactulose:

Lactulose (46,960 reports)

Browse all side effects of Lactulose:

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 Viith nerve paralysis:

Viith nerve paralysis (521 drugs)

Browse all the conditions that are associated with Viith nerve paralysis:

Viith nerve paralysis (837 conditions)

How the study uses the data?

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