Cellcept and Ranexa drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Cellcept (mycophenolate mofetil) and Ranexa (ranolazine). Common drug interactions include malaise among females and pain among males.

The phase IV clinical study analyzes what interactions people have when they take Cellcept and Ranexa. It is created by eHealthMe based on reports of 36 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 Ranexa?

Ranexa has active ingredients of ranolazine. It is often used in angina. eHealthMe is studying from 11,758 Ranexa users. Check the latest studies of Ranexa.



On Aug, 09, 2026

36 people who take Cellcept and Ranexa together, and have interactions are studied.

Cellcept and Ranexa drug interactions.

What are the common drug interactions of Cellcept and Ranexa, by gender? *:

female:

  1. Malaise (a feeling of general discomfort or uneasiness)
  2. Hospitalisation
  3. Pneumonia
  4. Sepsis (a severe blood infection that can lead to organ failure and death)
  5. Abdominal pain upper
  6. Crest syndrome (thick, dry and fibrous skin)
  7. Death
  8. Diabetes mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)
  9. Dyspnoea (difficult or laboured respiration)

male:

  1. Pain
  2. Arthralgia (joint pain)
  3. Gait disturbance
  4. Headache (pain in head)
  5. Hypoaesthesia (reduced sense of touch or sensation)
  6. Hypokinesia (decreased bodily movement)
  7. Sedation
  8. Urinary incontinence (inability to control the flow of urine and involuntary urination)
  9. Meningitis (inflammation of the protective membranes covering the brain and spinal cord, known collectively as the meninges)
  10. Nerve injury

What are the common drug interactions of Cellcept and Ranexa, by age (0-1 to 60+)? *:

0-1:

n/a

2-9:

n/a

10-19:

n/a

20-29:

n/a

30-39:

  1. Cardiac disorder
  2. Myocardial infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)

40-49:

  1. Chronic kidney disease
  2. Nephrogenic anaemia (anaemia due to kidney disease)
  3. Renal failure (kidney dysfunction)
  4. Dyspepsia (indigestion)
  5. Dyspnoea (difficult or laboured respiration)

50-59:

  1. Pneumonia
  2. Sepsis (a severe blood infection that can lead to organ failure and death)
  3. Blood glucose increased
  4. Crest syndrome (thick, dry and fibrous skin)
  5. Diabetes mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)
  6. Malaise (a feeling of general discomfort or uneasiness)

60+:

  1. Arthralgia (joint pain)
  2. Balance disorder
  3. Hypoaesthesia (reduced sense of touch or sensation)
  4. Hypokinesia (decreased bodily movement)
  5. Pain
  6. Sedation
  7. Urinary incontinence (inability to control the flow of urine and involuntary urination)
  8. Meningitis (inflammation of the protective membranes covering the brain and spinal cord, known collectively as the meninges)
  9. Nerve injury
  10. Arteriosclerosis coronary artery (thickening and hardening of arteries- coronary artery)

What are the existing conditions these people have? *

  1. Post Laminectomy Syndrome: 8 people, 22.22%
  2. Neuralgia (pain in one or more nerves): 8 people, 22.22%
  3. Spinal Osteoarthritis (joint cartilage loss in spine): 6 people, 16.67%
  4. Cardiac Failure Congestive: 6 people, 16.67%
  5. Psoriasis (immune-mediated disease that affects the skin): 5 people, 13.89%
  6. Nuclear Magnetic Resonance Imaging Abdominal: 4 people, 11.11%
  7. Chronic Renal Failure (kidney failure): 4 people, 11.11%
  8. Renal Artery Stenosis (narrowing of renal artery): 4 people, 11.11%
  9. Nuclear Magnetic Resonance Imaging Brain: 4 people, 11.11%
  10. Stable Angina (a constant chest pain): 4 people, 11.11%

* Approximation only. Some reports may have incomplete information.

Do you take Cellcept and Ranexa?

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Related studies:

Effectiveness of, side effects of, and alternative drugs to the 2 drugs:

Browse all drug interactions of Cellcept and Ranexa:

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 z

Sub-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 z

Browse all side effects of Ranexa:

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 z

Browse 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 z

Browse all interactions between Ranexa 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 z

How the study uses the data?

The study uses data from the FDA. It is based on mycophenolate mofetil and ranolazine (the active ingredients of Cellcept and Ranexa, respectively), and Cellcept and Ranexa (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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