Cellcept and Depakote drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Cellcept (mycophenolate mofetil) and Depakote (divalproex sodium). Common drug interactions include international normalised ratio increased among females and pain among males.
The phase IV clinical study analyzes what interactions people have when they take Cellcept and Depakote. It is created by eHealthMe based on reports of 90 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 Depakote?
Depakote has active ingredients of divalproex sodium. It is often used in bipolar disorder. eHealthMe is studying from 55,581 Depakote users. Check the latest studies of Depakote.
90 people who take Cellcept and Depakote together, and have interactions are studied.

What are the common drug interactions of Cellcept and Depakote, by gender? *:
female:
- International normalised ratio increased
- Limb discomfort (discomfort in leg)
- Loss of consciousness
- Lower limb fracture
- Oropharyngeal pain
- Pneumonia
- Pneumonia aspiration (bronchopneumonia that develops due to the entrance of foreign materials into the bronchial tree)
- Pruritus (severe itching of the skin)
- Pyrexia (fever)
- Seizure (abnormal excessive or synchronous neuronal activity in the brain)
male:
- Pain
- Back injury
- Cardiac failure congestive
- Fall
- Gastrointestinal disorder (functional problems of gastrointestinal tract)
- Graft complication
- Hospitalisation
- Hypertensive crisis
- Oxygen saturation decreased
- Pleural effusion (water on the lungs)
What are the common drug interactions of Cellcept and Depakote, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
- Laryngitis (inflammation of the larynx)
- Sinusitis (inflammation of sinus)
- Back injury
- Dehydration (dryness resulting from the removal of water)
- Depression
- Fall
- Gastrointestinal disorder (functional problems of gastrointestinal tract)
- Growth hormone deficiency
- Hospitalisation
- Kidney transplant rejection
20-29:
- Cardiac failure congestive
- Pleural effusion (water on the lungs)
- Pulmonary oedema (fluid accumulation in the lungs)
- Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body)
- Migraine (headache)
- Decreased appetite
- Depressed level of consciousness
- Diarrhoea
- Disease recurrence
- Local swelling (swelling at the site of some application of substance or injury)
30-39:
- Blindness unilateral
- Anxiety
- Depression
- Obsessive-compulsive disorder (an anxiety disorder characterized by intrusive thoughts that produce uneasiness, apprehension, fear, or worry;)
- Arthralgia (joint pain)
- Chronic kidney disease
- Pancreatic disorder
- Visual acuity reduced (reduced clearness of vision)
40-49:
- Anxiety
- Abdominal pain upper
- Anhedonia (inability to experience pleasure from activities usually found enjoyable)
- Arthralgia (joint pain)
- Blood glucose decreased
- Blood glucose fluctuation
- Burning sensation
- Cholestasis (a condition where bile cannot flow from the liver to the duodenum)
- Drug exposure during pregnancy
- Dry skin
50-59:
- Chills (felling of cold)
- Diabetic gastroparesis (paralysis of the muscles of the stomach caused by diabetes)
- Disease progression
- Drug ineffective
- Dyspnoea (difficult or laboured respiration)
- Fall
- Foot fracture
- Headache (pain in head)
- Hyperglycaemia (high blood sugar)
- Insomnia (sleeplessness)
60+:
- Bone marrow depression (decreased ability or inability of the bone marrow to produce blood cells)
- Anaemia (lack of blood)
- Hypertensive crisis
- International normalised ratio increased
- Mental status changes (general changes in brain function, such as confusion, amnesia (memory loss), loss of alertness, loss of orientation)
- Oedema peripheral (superficial swelling)
- Pneumonia aspiration (bronchopneumonia that develops due to the entrance of foreign materials into the bronchial tree)
- Acute respiratory distress syndrome
- Aphasia (damage to the parts of the brain that control language)
- Balance disorder
What are the existing conditions these people have? *
- Myasthenia Gravis (a chronic condition that causes muscles to tire and weaken easily): 10 people, 11.11%
- Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 6 people, 6.67%
- Seizures (abnormal excessive or synchronous neuronal activity in the brain): 5 people, 5.56%
* Approximation only. Some reports may have incomplete information.
Do you take Cellcept and Depakote?
- 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 Depakote:
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 Depakote:
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 Depakote 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 divalproex sodium (the active ingredients of Cellcept and Depakote, respectively), and Cellcept and Depakote (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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