Lactulose and Tekturna drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Lactulose (lactulose) and Tekturna (aliskiren hemifumarate). Common drug interactions include chronic kidney disease among females and chronic kidney disease among males.
The phase IV clinical study analyzes what interactions people have when they take Lactulose and Tekturna. It is created by eHealthMe based on reports of 18 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 Tekturna?
Tekturna has active ingredients of aliskiren hemifumarate. It is often used in high blood pressure. eHealthMe is studying from 4,730 Tekturna users. Check the latest studies of Tekturna.
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 >>>.
18 people who take Lactulose and Tekturna together, and have interactions are studied.

What are the common drug interactions of Lactulose and Tekturna, by gender? *:
female:
- Chronic kidney disease
- Renal failure (kidney dysfunction)
- Emotional disorder
- Fatigue (feeling of tiredness)
- Respiratory distress (difficulty in breathing)
- Restless legs syndrome (a powerful urge to move your legs)
- Tardive dyskinesia (a disorder that involves involuntary movements)
- Abdominal distension
- Abdominal pain
- Abdominal tenderness
male:
- Chronic kidney disease
- Nephrogenic anaemia (anaemia due to kidney disease)
- Vomiting
- Renal failure (kidney dysfunction)
- Acute myocardial infarction (acute heart attack)
- Coronary artery disease (plaque building up along the inner walls of the arteries of the heart, which narrows the arteries and restricts blood flow to the heart)
- Hyperparathyroidism secondary (an abnormally high concentration of parathyroid hormone in the blood, resulting in weakening of the bones through loss of calcium-secondary)
- Peritonitis (inflammation of the peritoneum, the thin tissue that lines the inner wall of the abdomen and covers most of the abdominal organs)
- Phlebitis (inflammation of the walls of a vein)
- Pleural effusion (water on the lungs)
What are the common drug interactions of Lactulose and Tekturna, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Chronic kidney disease
- Renal injury (kidney injury)
40-49:
- Chronic kidney disease
50-59:
- Pleural effusion (water on the lungs)
- Renal failure (kidney dysfunction)
- Chest pain
- Chronic kidney disease
- Dyspnoea (difficult or laboured respiration)
- Fatigue (feeling of tiredness)
- Fluid retention (an abnormal accumulation of fluid in the blood)
- Hyperparathyroidism secondary (an abnormally high concentration of parathyroid hormone in the blood, resulting in weakening of the bones through loss of calcium-secondary)
- Nephrogenic anaemia (anaemia due to kidney disease)
- Nephropathy (damage to or disease of a kidney)
60+:
- Chronic kidney disease
- Emotional disorder
- Blood urine present
- Coronary artery disease (plaque building up along the inner walls of the arteries of the heart, which narrows the arteries and restricts blood flow to the heart)
- Death
- Dry mouth
- Dysuria (painful or difficult urination)
- Eye disorder
- Fatigue (feeling of tiredness)
- Hyperparathyroidism secondary (an abnormally high concentration of parathyroid hormone in the blood, resulting in weakening of the bones through loss of calcium-secondary)
What are the existing conditions these people have? *
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 8 people, 44.44%
- Stress And Anxiety: 6 people, 33.33%
- Diabetes: 6 people, 33.33%
- High Blood Cholesterol: 5 people, 27.78%
- Infection: 5 people, 27.78%
- Hypersensitivity: 4 people, 22.22%
- Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 4 people, 22.22%
- Fluid Retention (an abnormal accumulation of fluid in the blood): 4 people, 22.22%
- Migraine (headache): 4 people, 22.22%
- Nasopharyngitis (inflammation of the nasopharynx): 4 people, 22.22%
* Approximation only. Some reports may have incomplete information.
Do you take Lactulose and Tekturna?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Lactulose and Tekturna:
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 zSub-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 zBrowse all side effects of Tekturna:
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 zBrowse 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 zBrowse all interactions between Tekturna 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 zHow the study uses the data?
The study uses data from the FDA. It is based on lactulose and aliskiren hemifumarate (the active ingredients of Lactulose and Tekturna, respectively), and Lactulose and Tekturna (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.
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