Centrum and Butrans drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Centrum (ascorbic acid; biotin; cyanocobalamin; dexpanthenol; ergocalciferol; folic acid; niacinamide; pyridoxine hydrochloride; riboflavin phosphate sodium; thiamine hydrochloride; vitamin a; vitamin e) and Butrans (buprenorphine). Common drug interactions include rash among females and somnolence among males.
The phase IV clinical study analyzes what interactions people have when they take Centrum and Butrans. It is created by eHealthMe based on reports of 21 people who take the same drugs from the FDA, and is updated regularly.
What is Centrum?
Centrum has active ingredients of ascorbic acid; biotin; cyanocobalamin; dexpanthenol; ergocalciferol; folic acid; niacinamide; pyridoxine hydrochloride; riboflavin phosphate sodium; thiamine hydrochloride; vitamin a; vitamin e. It is often used in vitamin supplementation. eHealthMe is studying from 34,686 Centrum users. Check the latest studies of Centrum.
What is Butrans?
Butrans has active ingredients of buprenorphine. It is often used in pain. eHealthMe is studying from 64,148 Butrans users. Check the latest studies of Butrans.
21 people who take Centrum and Butrans together, and have interactions are studied.

What are the common drug interactions of Centrum and Butrans, by gender? *:
female:
- Rash
- Application site discharge
- Application site discolouration
- Application site pain
- Application site pruritus (application site severe itching of the skin)
- Application site vesicles (small bubble within a cell at application site)
- Haemorrhage (bleeding)
- Drug dependence
- Drug ineffective
- Bacterial infection
male:
- Somnolence (a state of near-sleep, a strong desire for sleep)
- Accelerated hypertension (significant hypertension)
- Hepatic enzyme increased
- Hypersensitivity
- Infection
- Pneumonia aspiration (bronchopneumonia that develops due to the entrance of foreign materials into the bronchial tree)
- Tooth extraction
- Tooth infection
- Toothache (tooth pain)
- Urinary retention (the inability to completely or partially empty the bladder)
What are the common drug interactions of Centrum and Butrans, 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:
- Bacterial infection
- Gamma-glutamyltransferase increased
50-59:
- Bursitis (inflammation of a bursa, typically one in the knee, elbow, or shoulder)
- Carotid artery occlusion (artery blockage)
- Chronic kidney disease
- Deafness unilateral
- Drug ineffective
- Eye swelling
- Feeding disorder (when children refuse to eat certain food groups)
- Inflammation
- Insomnia (sleeplessness)
- Intervertebral disc operation
60+:
- Application site discharge
- Application site discolouration
- Dementia (madness)
- Dental caries
- Drug dependence
- Hepatic enzyme increased
- Hypersensitivity
- Infection
- Somnolence (a state of near-sleep, a strong desire for sleep)
- Tooth extraction
What are the existing conditions these people have? *
- Back Pain: 4 people, 19.05%
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 4 people, 19.05%
- High Blood Pressure: 4 people, 19.05%
- Diabetes: 3 people, 14.29%
- Neck Pain: 3 people, 14.29%
- Nausea (feeling of having an urge to vomit): 3 people, 14.29%
- High Blood Cholesterol: 3 people, 14.29%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 3 people, 14.29%
- Cataplexy (loss of muscle tone accompanied by full conscious awareness): 3 people, 14.29%
- Depression: 3 people, 14.29%
* Approximation only. Some reports may have incomplete information.
Do you take Centrum and Butrans?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Centrum and Butrans:
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 Centrum:
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 Butrans:
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 Centrum 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 Butrans 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 ascorbic acid; biotin; cyanocobalamin; dexpanthenol; ergocalciferol; folic acid; niacinamide; pyridoxine hydrochloride; riboflavin phosphate sodium; thiamine hydrochloride; vitamin a; vitamin e and buprenorphine (the active ingredients of Centrum and Butrans, respectively), and Centrum and Butrans (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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