Besponsa and Prograf drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Besponsa (inotuzumab ozogamicin) and Prograf (tacrolimus). Common drug interactions include cytokine release syndrome among females and venoocclusive liver disease among males.

The phase IV clinical study analyzes what interactions people have when they take Besponsa and Prograf. It is created by eHealthMe based on reports of 31 people who take the same drugs from the FDA, and is updated regularly.

What is Besponsa?

Besponsa has active ingredients of inotuzumab ozogamicin. eHealthMe is studying from 801 Besponsa users. Check the latest studies of Besponsa.

What is Prograf?

Prograf has active ingredients of tacrolimus. It is often used in kidney transplant. eHealthMe is studying from 42,230 Prograf users. Check the latest studies of Prograf.



On Jul, 04, 2026

31 people who take Besponsa and Prograf together, and have interactions are studied.

Besponsa and Prograf drug interactions.

What are the common drug interactions of Besponsa and Prograf, by gender? *:

female:

  1. Cytokine release syndrome (immediate complication occurring with the use of anti-t cell antibody infusions)
  2. Septic shock (shock due to blood infection)
  3. Venoocclusive liver disease (small veins in the liver are obstructed)
  4. Venoocclusive disease (small veins in the liver are obstructed)
  5. Thrombotic microangiopathy (a pathology that results in thrombosis in capillaries and arterioles, due to an endothelial injury)
  6. 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)
  7. Oral disorder (mouth disease)
  8. Pleural effusion (water on the lungs)
  9. Fluid retention (an abnormal accumulation of fluid in the blood)
  10. Hepatic vein occlusion (blockage of the hepatic vein)

male:

  1. Venoocclusive liver disease (small veins in the liver are obstructed)
  2. Engraftment syndrome (inflammatory condition during neutrophil recovery after hematopoietic stem cell transplantation)
  3. Alanine aminotransferase increased
  4. Chronic graft versus host disease in skin (damage by immune cells to skin after grafting)
  5. Pneumonia
  6. Platelet count decreased
  7. Fungal infection
  8. Meningitis bacterial (bacterial inflammation of the protective membranes covering the brain and spinal cord, known collectively as the meninges)
  9. Coma hepatic (accumulation in the bloodstream of toxic substances that are normally removed by the liver leads coma)
  10. 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)

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

0-1:

n/a

2-9:

  1. Fungal infection
  2. Meningitis bacterial (bacterial inflammation of the protective membranes covering the brain and spinal cord, known collectively as the meninges)
  3. Venoocclusive liver disease (small veins in the liver are obstructed)
  4. Pneumonia

10-19:

  1. Engraftment syndrome (inflammatory condition during neutrophil recovery after hematopoietic stem cell transplantation)
  2. Platelet count decreased
  3. Venoocclusive liver disease (small veins in the liver are obstructed)
  4. Coma hepatic (accumulation in the bloodstream of toxic substances that are normally removed by the liver leads coma)
  5. 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)
  6. Hepatic encephalopathy (spectrum of neuropsychiatric abnormalities in patients with liver failure)
  7. Hepatic failure (liver failure)
  8. Immune system disorder

20-29:

  1. Cytokine release syndrome (immediate complication occurring with the use of anti-t cell antibody infusions)
  2. Septic shock (shock due to blood infection)
  3. Venoocclusive disease (small veins in the liver are obstructed)
  4. Venoocclusive liver disease (small veins in the liver are obstructed)
  5. Thrombotic microangiopathy (a pathology that results in thrombosis in capillaries and arterioles, due to an endothelial injury)
  6. 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)
  7. Oral disorder (mouth disease)
  8. Fluid retention (an abnormal accumulation of fluid in the blood)
  9. Hepatic vein occlusion (blockage of the hepatic vein)
  10. Neutrophil count decreased (less than normal number of neutrophil a type of blood cell)

30-39:

n/a

40-49:

  1. Neutropenia (an abnormally low number of neutrophils)
  2. Tumour lysis syndrome (a group of metabolic complications that can occur after treatment of cancer, these complications are caused by the breakdown products of dying cancer cells)

50-59:

  1. Blood glucose increased
  2. Blood lactate dehydrogenase decreased
  3. Blood lactate dehydrogenase increased
  4. Blood potassium decreased
  5. Blood urea decreased
  6. Blood urea increased
  7. C-reactive protein increased
  8. Diarrhoea
  9. Gamma-glutamyltransferase increased
  10. 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)

60+:

  1. Alanine aminotransferase increased
  2. Chronic graft versus host disease in skin (damage by immune cells to skin after grafting)

What are the existing conditions these people have? *

  1. Acute Lymphocytic Leukaemia Recurrent (cancer in which the bone marrow makes too many lymphocytes-recurrent): 19 people, 61.29%
  2. Acute Lymphocytic Leukemia (All) (cancer of the white blood cells characterized by excess lymphoblasts): 9 people, 29.03%
  3. B Precursor Type Acute Leukaemia (lymphoid cancer): 6 people, 19.35%
  4. Immunodeficiency Disorders: 6 people, 19.35%
  5. Pain: 4 people, 12.90%
  6. Febrile Neutropenia (fever with reduced white blood cells): 4 people, 12.90%
  7. Constipation: 4 people, 12.90%
  8. Hyperuricaemia (level of uric acid in the blood that is abnormally high): 4 people, 12.90%
  9. 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): 4 people, 12.90%
  10. Cytokine Release Syndrome (immediate complication occurring with the use of anti-t cell antibody infusions): 3 people, 9.68%

* Approximation only. Some reports may have incomplete information.

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Related studies:

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

Browse all drug interactions of Besponsa and Prograf:

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 Besponsa:

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 Prograf:

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 Besponsa 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 Prograf 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 inotuzumab ozogamicin and tacrolimus (the active ingredients of Besponsa and Prograf, respectively), and Besponsa and Prograf (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.

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