Lactulose and Performance status decreased - a phase IV clinical study of FDA data

Summary:

Performance status decreased is reported as a side effect among people who take Lactulose (lactulose), especially for people who are male, 50-59 old, have been taking the drug for 1 - 6 months also take Morphine, and have Pain.

The phase IV clinical study analyzes which people have Performance status decreased 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 Performance status decreased?

Performance status decreased is found to be associated with 515 drugs and 636 conditions by eHealthMe. Check the latest studies of Performance status decreased.

On Jul, 17, 2026

46,694 people reported to have side effects when taking Lactulose.
Among them, 28 people (0.06%) have Performance status decreased.

Could Lactulose cause Performance status decreased?

Among these 28 people:

How long have people been on Lactulose when they have Performance status decreased? *

What is the gender of people who have Performance status decreased when taking Lactulose? *

female: 39.29 %
male: 60.71 %

What is the age of people who have Performance status decreased when taking Lactulose? *

What are other drugs people take besides Lactulose? *

What are other side effects people have besides Performance status decreased? *

Weight Decreased: 13 people, 46.43%
Weakness: 10 people, 35.71%
Fatigue (feeling of tiredness): 9 people, 32.14%
Nausea (feeling of having an urge to vomit): 9 people, 32.14%
Dyspnea (difficult or laboured breathing): 8 people, 28.57%
Appetite - Decreased (decreased appetite occurs when you have a reduced desire to eat): 7 people, 25.00%
Gait Disturbance: 7 people, 25.00%
Oedema Peripheral (superficial swelling): 6 people, 21.43%
Paraesthesia (sensation of tingling, tickling, prickling, pricking, or burning of a person's skin with no apparent long-term physical effect): 5 people, 17.86%
Hypoaesthesia (reduced sense of touch or sensation): 5 people, 17.86%

What are the existing conditions these people have? *

Pain: 5 people, 17.86%
Multiple Myeloma (cancer of the plasma cells): 4 people, 14.29%
Stress And Anxiety: 3 people, 10.71%
Muscle Spasms (muscle contraction): 3 people, 10.71%
Metastatic Renal Cell Carcinoma (spreadable kidney cell tumour): 2 people, 7.14%
Breast Cancer: 2 people, 7.14%
Nausea (feeling of having an urge to vomit): 2 people, 7.14%
Glioma (a type of tumour that starts in the brain or spine): 2 people, 7.14%
Uterine Leiomyosarcoma (uterus cancer of smooth muscle connective tissue): 1 person, 3.57%
Herpes Zoster: 1 person, 3.57%

* Approximation only. Some reports may have incomplete information.

Do you take Lactulose and have Performance status decreased?

- Check whether Performance status decreased 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 Performance status decreased:

Performance status decreased (515 drugs)

Browse all the conditions that are associated with Performance status decreased:

Performance status decreased (636 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.