Loniten and Protonix drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Loniten (minoxidil) and Protonix (pantoprazole sodium). Common drug interactions include activities of daily living impaired among females and chronic kidney disease among males.
The phase IV clinical study analyzes what interactions people have when they take Loniten and Protonix. It is created by eHealthMe based on reports of 30 people who take the same drugs from the FDA, and is updated regularly.
What is Loniten?
Loniten has active ingredients of minoxidil. eHealthMe is studying from 363 Loniten users. Check the latest studies of Loniten.
What is Protonix?
Protonix has active ingredients of pantoprazole sodium. It is often used in gastroesophageal reflux disease. eHealthMe is studying from 132,658 Protonix users. Check the latest studies of Protonix.
30 people who take Loniten and Protonix together, and have interactions are studied.

What are the common drug interactions of Loniten and Protonix, by gender? *:
female:
- Activities of daily living impaired
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Anxiety
- Chest pain
- Dry skin
- Emotional distress
- Joint contracture (a permanent shortening of a muscle or joint)
- Joint stiffness
- Mobility decreased (ability to move is reduced)
- Muscular weakness (muscle weakness)
male:
- Chronic kidney disease
- Renal failure (kidney dysfunction)
- Metabolic acidosis (body produces too much acid, or when the kidneys are not removing enough acid from the body)
- Myocardial infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)
- Weight bearing difficulty (difficulty due to weight of thigh fat deposition)
- Hyperparathyroidism secondary (an abnormally high concentration of parathyroid hormone in the blood, resulting in weakening of the bones through loss of calcium-secondary)
- Diarrhoea
- Drug hypersensitivity
- Dyspnoea (difficult or laboured respiration)
- Gout (uric acid crystals building up in the body)
What are the common drug interactions of Loniten and Protonix, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
- Pneumonia
- Gastroenteritis (inflammation of stomach and intestine)
- Gastrointestinal haemorrhage (bleeding gastrointestinal tract)
30-39:
- Anaemia (lack of blood)
- Hip arthroplasty
- Hyperkalaemia (damage to or disease of the kidney)
- Hypoxia (low oxygen in tissues)
- Leukopenia (less number of white blood cells in blood)
- Metabolic acidosis (body produces too much acid, or when the kidneys are not removing enough acid from the body)
- Weight bearing difficulty (difficulty due to weight of thigh fat deposition)
- Abdominal pain
- Blood pressure decreased
- Breath sounds
40-49:
- Drug hypersensitivity
- Nasal congestion (blockage of the nasal passages usually due to membranes lining the nose becoming swollen from inflamed blood vessels)
- Anaemia (lack of blood)
- Appetite disorder (abnormal eating habits)
- Arthralgia (joint pain)
- Asthenia (weakness)
- Chills (felling of cold)
- Chronic kidney disease
- Diarrhoea
- Dizziness
50-59:
- Activities of daily living impaired
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Anxiety
- Dry skin
- Emotional distress
- Joint contracture (a permanent shortening of a muscle or joint)
- Joint stiffness
- Mobility decreased (ability to move is reduced)
- Muscular weakness (muscle weakness)
- Nephrogenic systemic fibrosis (involves fibrosis of skin, joints, eyes due to kidney disease)
60+:
- Chronic kidney disease
- Renal injury (kidney injury)
- Anaphylactic reaction (serious allergic reaction)
- Myocardial infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)
- Nephrogenic anaemia (anaemia due to kidney disease)
- Renal failure (kidney dysfunction)
- Overdose
What are the existing conditions these people have? *
- Pain: 12 people, 40.00%
- High Blood Pressure: 11 people, 36.67%
- Diabetes: 9 people, 30.00%
- Anaemia (lack of blood): 8 people, 26.67%
- Nuclear Magnetic Resonance Imaging Brain: 6 people, 20.00%
- Chronic Obstructive Pulmonary Disease (a progressive disease that makes it hard to breathe): 6 people, 20.00%
- Nausea And Vomiting: 4 people, 13.33%
- Nausea (feeling of having an urge to vomit): 4 people, 13.33%
- High Blood Cholesterol: 4 people, 13.33%
- Haemolytic Uraemic Syndrome (blood clotting disease caused by e. coli infection, birth control pills, pneumonia, medications, and more): 4 people, 13.33%
* Approximation only. Some reports may have incomplete information.
Do you take Loniten and Protonix?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Loniten and Protonix:
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 Loniten:
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 Protonix:
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 Loniten 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 Protonix 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 zRelated publications that referenced our studies
- Dubrey SW, VanGriethuysen J, Edwards CM, "A hairy fall: syncope resulting from topical application of minoxidil", BMJ case reports, 2015 Sep .
- Dubrey SW, VanGriethuysen J, Edwards CM, "A hairy fall: syncope resulting from topical application of minoxidil", BMJ case reports, 2015 Sep .
How the study uses the data?
The study uses data from the FDA. It is based on minoxidil and pantoprazole sodium (the active ingredients of Loniten and Protonix, respectively), and Loniten and Protonix (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.
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