Topamax and Prohance drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Topamax (topiramate) and Prohance (gadoteridol). Common drug interactions include deformity among females and nephrogenic systemic fibrosis among males.
The phase IV clinical study analyzes what interactions people have when they take Topamax and Prohance. It is created by eHealthMe based on reports of 24 people who take the same drugs from the FDA, and is updated regularly.
What is Topamax?
Topamax has active ingredients of topiramate. It is often used in migraine. eHealthMe is studying from 58,954 Topamax users. Check the latest studies of Topamax.
What is Prohance?
Prohance has active ingredients of gadoteridol. eHealthMe is studying from 3,734 Prohance users. Check the latest studies of Prohance.
24 people who take Topamax and Prohance together, and have interactions are studied.

What are the common drug interactions of Topamax and Prohance, by gender? *:
female:
- Deformity (disfigurement)
- Extremity contracture (permanent shortening of a muscle or joint of arms and legs)
- Hyperkeratosis (thickening of the outer layer of the skin)
- Joint range of motion decreased (disease of joint movement)
- Joint stiffness
- Muscular weakness (muscle weakness)
- Musculoskeletal stiffness (stiffness of the body's muscles, joints, tendons, ligaments and nerves)
- Nephrogenic systemic fibrosis (involves fibrosis of skin, joints, eyes due to kidney disease)
- Oedema (fluid collection in tissue)
- Oedema peripheral (superficial swelling)
male:
- Nephrogenic systemic fibrosis (involves fibrosis of skin, joints, eyes due to kidney disease)
- Cardiac arrest
- Pulmonary fibrosis (formation or development of excess fibrous connective tissue (fibrosis) in the lungs)
- Skin tightness
- Subcutaneous nodule
- Xerosis (abnormal dryness of the skin or mucus membranes)
- Endocardial fibrosis (cardiac fibrosis refers to an abnormal thickening of the heart valves)
- Joint contracture (a permanent shortening of a muscle or joint)
- Skin fibrosis (fibrous tissue formation on skin)
- Discomfort
What are the common drug interactions of Topamax and Prohance, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
- Nephrogenic systemic fibrosis (involves fibrosis of skin, joints, eyes due to kidney disease)
- Cardiac arrest
- Fibrosis (formation of excess fibrous connective tissue in an organ or tissue)
- Metaplasia (change in the type of adult cells in a tissue to a form abnormal for that tissue)
- Mobility decreased (ability to move is reduced)
- Muscle contracture (a permanent shortening of a muscle)
- Myocardial fibrosis (a condition in which the heart's muscle cells are impaired)
- Pain in extremity
- Pulmonary fibrosis (formation or development of excess fibrous connective tissue (fibrosis) in the lungs)
- Skin induration (an abnormally hard spot or area on the skin)
20-29:
n/a
30-39:
- Skin hypertrophy (skin cells enlarges)
- Skin induration (an abnormally hard spot or area on the skin)
- Deformity (disfigurement)
- Hyperkeratosis (thickening of the outer layer of the skin)
- Joint stiffness
- Muscular weakness (muscle weakness)
- Musculoskeletal stiffness (stiffness of the body's muscles, joints, tendons, ligaments and nerves)
- Rash
- Skin discolouration (change of skin colour)
- Joint contracture (a permanent shortening of a muscle or joint)
40-49:
- Anaphylactoid reaction (type of anaphylaxis that does not involve an allergic reaction but is due to direct mast cell degranulation)
- Chest pain
- Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body)
50-59:
n/a
60+:
n/a
What are the existing conditions these people have? *
- Catheter Related Complication: 8 people, 33.33%
- Joint Pain: 8 people, 33.33%
- Pain: 6 people, 25.00%
- Nuclear Magnetic Resonance Imaging Abdominal: 6 people, 25.00%
- Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body): 5 people, 20.83%
- Weight Increased: 4 people, 16.67%
- Dry Skin: 4 people, 16.67%
- Conductive Deafness (deafness due to a problem in conducting sound waves): 4 people, 16.67%
- Dizziness: 4 people, 16.67%
- Dry Eyes (lack of adequate tears): 4 people, 16.67%
* Approximation only. Some reports may have incomplete information.
Do you take Topamax and Prohance?
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Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Topamax and Prohance:
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 Topamax:
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 Prohance:
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 Topamax 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 Prohance 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
- Baloch M, Siddiqui MA, "Topiramate induced sudden loss of vision", JPMA, 2012 Oct .
- Kocamaz, M., & Karadag, O., "Topiramate-Induced Acute Myopia, Diplopia, and Photosensitivity: A Case Report", Beyoglu Eye Journal, 2019 Jan .
- Baloch M, Siddiqui MA, "Topiramate induced sudden loss of vision", JPMA, 2012 Oct .
- Kocamaz, M., & Karadag, O., "Topiramate-Induced Acute Myopia, Diplopia, and Photosensitivity: A Case Report", Beyoglu Eye Journal, 2019 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on topiramate and gadoteridol (the active ingredients of Topamax and Prohance, respectively), and Topamax and Prohance (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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