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Could Cellcept, Ursodiol together cause Blood bilirubin increased?

This is a real world study of Blood bilirubin increased among people who take Cellcept, Ursodiol. The study is created by eHealthMe based on 45 reports from FDA and social media.

What are the drugs

Cellcept (latest outcomes from 15,791 users) has active ingredients of mycophenolate mofetil. It is often used in systemic lupus erythematosus.

Ursodiol (latest outcomes from 3,436 users) has active ingredients of ursodiol. It is often used in biliary cirrhosis primary.

On Oct, 31, 2014: 675 people reported to have side effects when taking Cellcept, Ursodiol. Among them, 45 people (6.67%) have Blood Bilirubin Increased.

Trend of Blood bilirubin increased in Cellcept, Ursodiol

Gender of people who have Blood bilirubin increased when taking the drugs * :

FemaleMale
Blood bilirubin increased27%73%

Age of people who have Blood bilirubin increased when taking the drugs * :

0-12-910-1920-2930-3940-4950-5960+
Blood bilirubin increased0%0%14%14%11%6%25%31%

Severity of Blood bilirubin increased when taking the drugs ** :

n/a

How people recovered from Blood bilirubin increased ** :

n/a

* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

More about the drug combination: Cellcept, Ursodiol drug interactions

You can also:

NOTE: The study is based on active ingredients. Other drugs that have the same active ingredients are also considered.

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, and has not been supported by scientific studies or clinical trials unless otherwise stated. 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.

You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.

 

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