Lactulose and Blood phosphorus increased - a phase IV clinical study of FDA data

Summary:

Blood phosphorus increased is reported as a side effect among people who take Lactulose (lactulose), especially for people who are male, 60+ old, have been taking the drug for < 1 month also take Tylenol, and have Acute lymphocytic leukemia (all).

The phase IV clinical study analyzes which people have Blood phosphorus increased 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 Blood phosphorus increased?

Blood phosphorus increased is found to be associated with 443 drugs and 529 conditions by eHealthMe. Check the latest studies of Blood phosphorus increased.

On Jul, 04, 2026

46,694 people reported to have side effects when taking Lactulose.
Among them, 24 people (0.05%) have Blood phosphorus increased.

Could Lactulose cause Blood phosphorus increased?

Among these 24 people:

How long have people been on Lactulose when they have Blood phosphorus increased? *

What is the gender of people who have Blood phosphorus increased when taking Lactulose? *

female: 17.39 %
male: 82.61 %

What is the age of people who have Blood phosphorus increased when taking Lactulose? *

What are other drugs people take besides Lactulose? *

What are other side effects people have besides Blood phosphorus increased? *

Blood Creatinine Increased: 12 people, 50.00%
Haemoglobin Decreased: 10 people, 41.67%
Blood Calcium Decreased: 10 people, 41.67%
Hyperkalemia (damage to or disease of the kidney): 7 people, 29.17%
Thrombocytopenia (decrease of platelets in blood): 7 people, 29.17%
Haematocrit Decreased: 7 people, 29.17%
Blood Urea Increased: 7 people, 29.17%
Lymphocyte Count Decreased: 6 people, 25.00%
White Blood Cell Count Decreased: 6 people, 25.00%
Blood Sodium Decreased: 5 people, 20.83%

What are the existing conditions these people have? *

Acute Lymphocytic Leukemia (All) (cancer of the white blood cells characterized by excess lymphoblasts): 3 people, 12.50%
High Blood Pressure: 2 people, 8.33%
Blood Phosphorus Abnormal: 2 people, 8.33%
Blood Uric Acid Increased: 2 people, 8.33%
Cardiac Disorder: 2 people, 8.33%
Multiple Myeloma (cancer of the plasma cells): 2 people, 8.33%
Metastatic Renal Cell Carcinoma (spreadable kidney cell tumour): 2 people, 8.33%
Rashes (redness): 2 people, 8.33%
Hepatic Cirrhosis (chronic liver disease characterized by replacement of liver tissue by fibrosis, scar tissue): 2 people, 8.33%
Crohn's Disease (a condition that causes inflammation of the gastrointestinal tract): 1 person, 4.17%

* Approximation only. Some reports may have incomplete information.

Do you take Lactulose and have Blood phosphorus increased?

- Check whether Blood phosphorus increased is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
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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 Blood phosphorus increased:

Blood phosphorus increased (443 drugs)

Browse all the conditions that are associated with Blood phosphorus increased:

Blood phosphorus increased (529 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.