Temaz and Multihance drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Temaz (temazepam) and Multihance (gadobenate dimeglumine). Common drug interactions include nephrogenic systemic fibrosis among females and nephrogenic systemic fibrosis among males.
The phase IV clinical study analyzes what interactions people have when they take Temaz and Multihance. It is created by eHealthMe based on reports of 35 people who take the same drugs from the FDA, and is updated regularly.
What is Temaz?
Temaz has active ingredients of temazepam. It is often used in insomnia. eHealthMe is studying from 42,293 Temaz users. Check the latest studies of Temaz.
What is Multihance?
Multihance has active ingredients of gadobenate dimeglumine. eHealthMe is studying from 5,786 Multihance users. Check the latest studies of Multihance.
35 people who take Temaz and Multihance together, and have interactions are studied.

What are the common drug interactions of Temaz and Multihance, by gender? *:
female:
- Nephrogenic systemic fibrosis (involves fibrosis of skin, joints, eyes due to kidney disease)
- Emotional distress
- Mobility decreased (ability to move is reduced)
- Pain
- Anxiety
- Skin discolouration (change of skin colour)
- Asthenia (weakness)
- Fibrosis (formation of excess fibrous connective tissue in an organ or tissue)
- General physical health deterioration (weak health status)
- Oedema peripheral (superficial swelling)
male:
- Nephrogenic systemic fibrosis (involves fibrosis of skin, joints, eyes due to kidney disease)
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Muscle tightness
- Myosclerosis (hardening of muscle tissue)
- Oedema peripheral (superficial swelling)
- Skin induration (an abnormally hard spot or area on the skin)
- Skin tightness
- Activities of daily living impaired
- Fatigue (feeling of tiredness)
- Frustration (a form of poorly expressed anger)
What are the common drug interactions of Temaz and Multihance, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Anxiety
- Emotional distress
- Fibrosis (formation of excess fibrous connective tissue in an organ or tissue)
- General physical health deterioration (weak health status)
- Mobility decreased (ability to move is reduced)
- Nephrogenic systemic fibrosis (involves fibrosis of skin, joints, eyes due to kidney disease)
- Pain
- Scar
- Bronchopneumonia (inflammation of the lungs, arising in the bronchi or bronchioles)
40-49:
- Nephrogenic systemic fibrosis (involves fibrosis of skin, joints, eyes due to kidney disease)
- Anxiety
- Emotional distress
- Injury
- Pain
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Extremity contracture (permanent shortening of a muscle or joint of arms and legs)
- Joint contracture (a permanent shortening of a muscle or joint)
- Joint range of motion decreased (disease of joint movement)
- Muscle fibrosis (fibrous muscle)
50-59:
- Anxiety
- Asthenia (weakness)
- Emotional distress
- Joint range of motion decreased (disease of joint movement)
- Muscle tightness
- Musculoskeletal stiffness (stiffness of the body's muscles, joints, tendons, ligaments and nerves)
- Quality of life decreased
- Skin discolouration (change of skin colour)
- Fatigue (feeling of tiredness)
- Skin hyperpigmentation (disorders affect the colour of your skin)
60+:
- Hypersensitivity
- Hypotension (abnormally low blood pressure)
- Hypoxia (low oxygen in tissues)
- Tachycardia (a heart rate that exceeds the range of 100 beats/min)
What are the existing conditions these people have? *
- Nuclear Magnetic Resonance Imaging Brain: 9 people, 25.71%
- Nuclear Magnetic Resonance Imaging Abdominal: 9 people, 25.71%
- Kidney Transplant Rejection: 4 people, 11.43%
- Osteomyelitis (infection of bone): 2 people, 5.71%
- Diabetic Foot: 2 people, 5.71%
* Approximation only. Some reports may have incomplete information.
Do you take Temaz and Multihance?
- 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:
- Temaz (42,293 reports)
- Multihance (5,786 reports)
Browse all drug interactions of Temaz and Multihance:
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 Temaz:
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 Multihance:
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 Temaz 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 Multihance 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 temazepam and gadobenate dimeglumine (the active ingredients of Temaz and Multihance, respectively), and Temaz and Multihance (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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