Tacrolimus and Full blood count abnormal - a phase IV clinical study of FDA data

Summary:

Full blood count abnormal is reported as a side effect among people who take Tacrolimus (tacrolimus), especially for people who are female, 60+ old, also take Cresemba, and have Acute myeloid leukaemia.

The phase IV clinical study analyzes which people have Full blood count abnormal when taking Tacrolimus. It is created by eHealthMe based on reports of 115,828 people who have side effects when taking Tacrolimus from the FDA, and is updated regularly.

What is Tacrolimus?

Tacrolimus has active ingredients of tacrolimus. It is often used in kidney transplant. eHealthMe is studying from 116,161 Tacrolimus users. Check the latest studies of Tacrolimus.

What is Full blood count abnormal?

Full blood count abnormal is found to be associated with 628 drugs and 378 conditions by eHealthMe. Check the latest studies of Full blood count abnormal.

eHealthMe: drug outcomes in the real world

eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.

On Sep, 01, 2026

115,828 people reported to have side effects when taking Tacrolimus.
Among them, 14 people (0.01%) have Full blood count abnormal.

Could Tacrolimus cause Full blood count abnormal?

Among these 14 people:

What is the gender of people who have Full blood count abnormal when taking Tacrolimus? *

female: 53.85 %
male: 46.15 %

What is the age of people who have Full blood count abnormal when taking Tacrolimus? *

What are other drugs people take besides Tacrolimus? *

What are other side effects people have besides Full blood count abnormal? *

Thrombocytopenia (decrease of platelets in blood): 7 people, 50.00%
Haemoglobin Decreased: 6 people, 42.86%
Diarrhea: 6 people, 42.86%
Urinary Tract Infection: 5 people, 35.71%
Fall: 5 people, 35.71%
Agranulocytosis (a deficiency of granulocytes in the blood, causing increased vulnerability to infection): 1 person, 7.14%
Bacteraemia (presence of bacteria in the blood): 1 person, 7.14%
Blood Glucose Increased: 1 person, 7.14%
Bone Marrow Failure: 1 person, 7.14%
Circulatory Collapse: 1 person, 7.14%

What are the existing conditions these people have? *

Neuropathy Peripheral (surface nerve damage): 5 people, 35.71%
Mantle Cell Lymphoma (cancer of lymphocytes, a type of white blood cell): 5 people, 35.71%
Acute Myeloid Leukaemia (acute cancer in which the bone marrow makes abnormal myeloblasts): 5 people, 35.71%
Graft Versus Host Disease (the donated bone marrow or stem cells view the recipient's body as foreign, and the donated cells/bone marrow attack the body): 2 people, 14.29%
Acute Lymphocytic Leukemia (All) (cancer of the white blood cells characterized by excess lymphoblasts): 2 people, 14.29%
Schizophrenia (a mental disorder characterized by a breakdown of thought processes): 1 person, 7.14%
Kidney Transplant Rejection: 1 person, 7.14%

* Approximation only. Some reports may have incomplete information.

Do you take Tacrolimus and have Full blood count abnormal?

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Related studies:

Effectiveness of, long term effects of, and alternative drugs to Tacrolimus:

Tacrolimus (116,161 reports)

Browse all side effects of Tacrolimus:

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 the drugs that are associated with Full blood count abnormal:

Full blood count abnormal (628 drugs)

Browse all the conditions that are associated with Full blood count abnormal:

Full blood count abnormal (378 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on tacrolimus (the active ingredients of Tacrolimus) and Tacrolimus (the brand name). 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.