Cellcept and Soma drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Cellcept (mycophenolate mofetil) and Soma (carisoprodol). Common drug interactions include brain injury among females and electrocardiogram qt prolonged among males.
The phase IV clinical study analyzes what interactions people have when they take Cellcept and Soma. It is created by eHealthMe based on reports of 42 people who take the same drugs from the FDA, and is updated regularly.
What is Cellcept?
Cellcept has active ingredients of mycophenolate mofetil. It is often used in systemic lupus erythematosus. eHealthMe is studying from 41,872 Cellcept users. Check the latest studies of Cellcept.
What is Soma?
Soma has active ingredients of carisoprodol. It is often used in muscle spasms. eHealthMe is studying from 17,137 Soma users. Check the latest studies of Soma.
42 people who take Cellcept and Soma together, and have interactions are studied.

What are the common drug interactions of Cellcept and Soma, by gender? *:
female:
- Brain injury
- Cardiac disorder
- Cardiovascular disorder (heart diseases)
- Cerebrovascular accident (sudden death of some brain cells due to lack of oxygen when the blood flow to the brain is impaired by blockage or rupture)
- Chronic inflammatory demyelinating polyradiculoneuropathy (long lasting infection of nerves outside brain and spinal cord)
- Depression
- Dizziness
- Drug administration error
- Drug effect decreased
- Dysphonia (speech disorder attributable to a disorder of phonation)
male:
- Electrocardiogram qt prolonged
- Device related infection
- Urinary tract infection
- Abdominal pain
- Abdominal pain upper
- Acne (skin problems that cause pimples)
- Asthenia (weakness)
- Blindness transient (sudden loss of vision)
- Blood cholesterol increased
- Blood creatinine decreased
What are the common drug interactions of Cellcept and Soma, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Hysterectomy
- Lupus nephritis (a chronic inflammatory autoimmune disorder that may affect kidney tissue)
- Spinal fracture (fracture in one of vertebrae)
- Therapeutic response unexpected
- Transaminases increased
- Device related infection
- Hereditary angioedema (recurrent episodes of severe swelling)
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Amenorrhoea (absence of a menstrual period in a woman of reproductive age)
- Arthralgia (joint pain)
40-49:
- Drug hypersensitivity
- Chest pain
- Rash
- Vomiting
- Coma (state of unconsciousness lasting more than six hours)
- Diarrhoea
- Eating disorder
- Encephalitis (inflammation of the brain)
- Hypoaesthesia oral (reduced sense of touch or sensation in mouth)
- Immunosuppression
50-59:
- Electrocardiogram qt prolonged
- Gastrointestinal hypomotility (less activity of the intestinal tract)
- Obstructive airways disorder (a progressive disease that makes it hard to breathe)
- Productive cough
- Pyrexia (fever)
- Sarcoidosis (an inflammatory disease that affects multiple organs in the body, but mostly the lungs and lymph glands)
- Small intestinal obstruction (blockage in small intestine)
- Urinary tract infection
- Abdominal discomfort
- Blindness
60+:
- Abdominal pain upper
- Blood creatinine decreased
- Cytomegalovirus infection
- Dehydration (dryness resulting from the removal of water)
- Device related infection
- Mental status changes (general changes in brain function, such as confusion, amnesia (memory loss), loss of alertness, loss of orientation)
- Muscular weakness (muscle weakness)
- Pneumonia
- Renal failure (kidney dysfunction)
- Skin cancer
What are the existing conditions these people have? *
- Pain: 16 people, 38.10%
- Depression: 7 people, 16.67%
- Neuropathy Peripheral (surface nerve damage): 5 people, 11.90%
- Systemic Sclerosis (Scleroderma) (an autoimmune or connective tissue disease. it is characterized by thickening of the skin): 4 people, 9.52%
- Dyspnea (difficult or laboured breathing): 4 people, 9.52%
- Essential Hypertension (primary hypertension): 4 people, 9.52%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 4 people, 9.52%
- Hereditary Angioedema (recurrent episodes of severe swelling): 4 people, 9.52%
- High Blood Pressure: 4 people, 9.52%
- Primary Pulmonary Hypertension (primary high blood pressure that affects the arteries in the lungs and the right side of your heart): 4 people, 9.52%
* Approximation only. Some reports may have incomplete information.
Do you take Cellcept and Soma?
- 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:
Browse all drug interactions of Cellcept and Soma:
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 Cellcept:
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 Soma:
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 Cellcept 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 Soma 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 mycophenolate mofetil and carisoprodol (the active ingredients of Cellcept and Soma, respectively), and Cellcept and Soma (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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