Lactulose and Pegintron drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Lactulose (lactulose) and Pegintron (peginterferon alfa-2b). Common drug interactions include haemoglobin decreased among females and weight decreased among males.

The phase IV clinical study analyzes what interactions people have when they take Lactulose and Pegintron. It is created by eHealthMe based on reports of 29 people who take the same drugs 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 Pegintron?

Pegintron has active ingredients of peginterferon alfa-2b. It is often used in hepatitis c. eHealthMe is studying from 10,326 Pegintron users. Check the latest studies of Pegintron.



On Aug, 02, 2026

29 people who take Lactulose and Pegintron together, and have interactions are studied.

Lactulose and Pegintron drug interactions.

What are the common drug interactions of Lactulose and Pegintron, by gender? *:

female:

  1. Haemoglobin decreased
  2. Pyrexia (fever)
  3. Urinary tract infection
  4. White blood cell count decreased
  5. Blood bilirubin increased
  6. Disseminated intravascular coagulation (systemic activation of blood coagulation)
  7. Neutrophil count decreased (less than normal number of neutrophil a type of blood cell)
  8. Platelet count decreased
  9. Sepsis (a severe blood infection that can lead to organ failure and death)
  10. Stomatitis (inflammation of mucous membrane of mouth)

male:

  1. Weight decreased
  2. Asthenia (weakness)
  3. Hyperammonaemia
  4. Infection reactivation
  5. Intervertebral discitis (infection in the intervertebral disc space)
  6. Diarrhoea
  7. Headache (pain in head)
  8. Infection
  9. Mobility decreased (ability to move is reduced)
  10. Nausea (feeling of having an urge to vomit)

What are the common drug interactions of Lactulose and Pegintron, by age (0-1 to 60+)? *:

0-1:

n/a

2-9:

n/a

10-19:

n/a

20-29:

n/a

30-39:

n/a

40-49:

  1. Gastrointestinal haemorrhage (bleeding gastrointestinal tract)
  2. Hyperuricaemia (level of uric acid in the blood that is abnormally high)
  3. Renal impairment (severely reduced kidney function)

50-59:

  1. Headache (pain in head)
  2. Pain
  3. Pyrexia (fever)
  4. Anaemia (lack of blood)
  5. Back pain
  6. Brain death
  7. Chills (felling of cold)
  8. Chronic kidney disease
  9. Death
  10. Flatulence (flatus expelled through the anus)

60+:

  1. Haemoglobin decreased
  2. Urinary tract infection
  3. Asthenia (weakness)
  4. Fatigue (feeling of tiredness)
  5. Activities of daily living impaired
  6. Anaemia (lack of blood)
  7. Atelectasis (partial or complete collapse of the lung)
  8. Blood glucose increased
  9. Cerebrovascular accident (sudden death of some brain cells due to lack of oxygen when the blood flow to the brain is impaired by blockage or rupture)
  10. Cough

What are the existing conditions these people have? *

  1. Hepatic Cirrhosis (chronic liver disease characterized by replacement of liver tissue by fibrosis, scar tissue): 3 people, 10.34%
  2. Pain: 2 people, 6.90%
  3. Itching: 2 people, 6.90%
  4. Iron Deficiency Anaemia: 2 people, 6.90%
  5. Insomnia (sleeplessness): 2 people, 6.90%
  6. Hiv Infection: 2 people, 6.90%
  7. Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 2 people, 6.90%
  8. Gastritis (inflammation of stomach): 2 people, 6.90%
  9. Anaemia (lack of blood): 2 people, 6.90%

* Approximation only. Some reports may have incomplete information.

Do you take Lactulose and Pegintron?

- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously



Related studies:

Effectiveness of, side effects of, and alternative drugs to the 2 drugs:

Browse all drug interactions of Lactulose and Pegintron:

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

Sub-studies by gender and age:

Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

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 side effects of Pegintron:

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 interactions between Lactulose and drugs from A to Z:

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 interactions between Pegintron and drugs from A to Z:

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

How the study uses the data?

The study uses data from the FDA. It is based on lactulose and peginterferon alfa-2b (the active ingredients of Lactulose and Pegintron, respectively), and Lactulose and Pegintron (the brand names). 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.



Recent studies on eHealthMe: