Thiotepa and Azacitidine drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Thiotepa (thiotepa) and Azacitidine (azacitidine). Common drug interactions include nausea among females and blood bilirubin decreased among males.

The phase IV clinical study analyzes what interactions people have when they take Thiotepa and Azacitidine. It is created by eHealthMe based on reports of 75 people who take the same drugs from the FDA, and is updated regularly.

What is Thiotepa?

Thiotepa has active ingredients of thiotepa. eHealthMe is studying from 8,097 Thiotepa users. Check the latest studies of Thiotepa.

What is Azacitidine?

Azacitidine has active ingredients of azacitidine. eHealthMe is studying from 17,184 Azacitidine users. Check the latest studies of Azacitidine.



On Jul, 19, 2026

75 people who take Thiotepa and Azacitidine together, and have interactions are studied.

Thiotepa and Azacitidine drug interactions.

What are the common drug interactions of Thiotepa and Azacitidine, by gender? *:

female:

  1. Nausea (feeling of having an urge to vomit)
  2. Acute graft versus host disease (acute complication following an allogeneic tissue/blood transplant)
  3. Cardiac failure
  4. Cardiomyopathy (weakening of the heart muscle)
  5. Ejection fraction decreased (systolic heart failure)
  6. Chronic graft versus host disease (immune cells attack the host's body cells after transplant)
  7. Oedema peripheral (superficial swelling)
  8. Drug ineffective
  9. Graft versus host disease in skin (the donated bone marrow or stem cells view the recipient's body as foreign, and the donated cells/bone marrow attack the skin)
  10. Calculus urinary (stone in urinary system)

male:

  1. Blood bilirubin decreased
  2. Hepatic failure (liver failure)
  3. Bone marrow failure
  4. Basal cell carcinoma (a skin cancer, it rarely metastasizes or kills)
  5. Deafness
  6. Odontogenic cyst (a group of jaw cysts that are formed from tissues of teeth development)
  7. Second primary malignancy (after getting cure a cancer, a new cancer development)
  8. Acute graft versus host disease (acute complication following an allogeneic tissue/blood transplant)
  9. Ascites (accumulation of fluid in the abdominal cavity)
  10. Cytogenetic abnormality

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

0-1:

  1. Drug ineffective
  2. Acute myeloid leukaemia (acute cancer in which the bone marrow makes abnormal myeloblasts)
  3. Disease progression

2-9:

  1. Clostridium difficile colitis (inflammation of colon by clostridium difficile bacteria infection)
  2. Hepatitis (inflammation of the liver)
  3. Fungaemia (fungi circulate in the blood)
  4. Hepatic failure (liver failure)
  5. Nausea (feeling of having an urge to vomit)
  6. Abdominal distension
  7. Acute myeloid leukaemia (acute cancer in which the bone marrow makes abnormal myeloblasts)
  8. Hepatomegaly (abnormal enlargement of the liver)
  9. Malignant neoplasm progression (cancer tumour came back)
  10. Venoocclusive disease (small veins in the liver are obstructed)

10-19:

  1. Drug ineffective
  2. Nausea (feeling of having an urge to vomit)
  3. Vomiting
  4. Deafness
  5. Myelodysplastic syndrome (a group of conditions that occur when the blood-forming cells in the bone marrow are damaged)
  6. Osteosarcoma (a cancerous (malignant) bone tumour)
  7. Disease progression
  8. Acute graft versus host disease (acute complication following an allogeneic tissue/blood transplant)
  9. Bone marrow failure
  10. Cytogenetic abnormality

20-29:

  1. Blood bilirubin decreased
  2. Venoocclusive disease (small veins in the liver are obstructed)
  3. Aplasia (defective development or congenital absence of an organ or tissue)
  4. Drug ineffective
  5. Hepatic failure (liver failure)
  6. Renal failure (kidney dysfunction)
  7. Respiratory failure (inadequate gas exchange by the respiratory system)
  8. Venoocclusive liver disease (small veins in the liver are obstructed)
  9. Bone marrow failure
  10. Graft versus host disease in skin (the donated bone marrow or stem cells view the recipient's body as foreign, and the donated cells/bone marrow attack the skin)

30-39:

  1. Acute graft versus host disease in intestine (acute complication in intestine following an allogeneic tissue/blood transplant)
  2. Acute graft versus host disease in skin (acute complication on skin following an allogeneic tissue/blood transplant)
  3. Blood bilirubin increased
  4. Rectal haemorrhage (bleeding from anus)
  5. Shock haemorrhagic (a life-threatening condition with symptoms like low blood pressure, weakness, shallow breathing, cold, clammy skin due to excess bleeding)
  6. Staphylococcal bacteraemia (a bacterial infection of blood)
  7. Venoocclusive liver disease (small veins in the liver are obstructed)

40-49:

  1. Acute graft versus host disease (acute complication following an allogeneic tissue/blood transplant)
  2. Chronic graft versus host disease (immune cells attack the host's body cells after transplant)
  3. Oedema peripheral (superficial swelling)
  4. Calculus urinary (stone in urinary system)
  5. Diarrhoea
  6. Febrile neutropenia (fever with reduced white blood cells)
  7. Graft versus host disease in skin (the donated bone marrow or stem cells view the recipient's body as foreign, and the donated cells/bone marrow attack the skin)
  8. Nausea (feeling of having an urge to vomit)
  9. Pyrexia (fever)
  10. Encephalitis viral (inflammation of the brain due to viral infection)

50-59:

  1. Pulmonary veno-occlusive disease (obstructive disease of the pulmonary veins)
  2. Acute graft versus host disease in liver (acute complication in liver following an allogeneic tissue/blood transplant)
  3. Acute graft versus host disease in skin (acute complication on skin following an allogeneic tissue/blood transplant)
  4. Pulmonary hypertension (increase in blood pressure in the lung artery)
  5. Chronic graft versus host disease in skin (damage by immune cells to skin after grafting)
  6. Headache (pain in head)
  7. Hypersensitivity
  8. Neutropenia (an abnormally low number of neutrophils)
  9. Pancytopenia (medical condition in which there is a reduction in the number of red and white blood cells, as well as platelets)
  10. Rash maculo-papular (red area on the skin that is covered with small confluent bumps)

60+:

  1. Cardiac failure
  2. Cardiomyopathy (weakening of the heart muscle)
  3. Epstein-barr virus infection
  4. Pleural effusion (water on the lungs)
  5. Respiratory failure (inadequate gas exchange by the respiratory system)
  6. Ejection fraction decreased (systolic heart failure)
  7. Ascites (accumulation of fluid in the abdominal cavity)
  8. Hepatic failure (liver failure)
  9. Pericardial effusion (fluid around the heart)
  10. Hepatotoxicity (chemical-driven liver damage)

What are the existing conditions these people have? *

  1. Acute Myeloid Leukaemia (acute cancer in which the bone marrow makes abnormal myeloblasts): 39 people, 52.00%
  2. Bone Marrow Conditioning Regimen: 30 people, 40.00%
  3. Myelodysplastic Syndrome (a group of conditions that occur when the blood-forming cells in the bone marrow are damaged): 18 people, 24.00%
  4. Nausea (feeling of having an urge to vomit): 12 people, 16.00%
  5. Febrile Neutropenia (fever with reduced white blood cells): 12 people, 16.00%
  6. Chronic Myeloid Leukaemia (long lasting type of cancer that starts in the blood-forming cells of the bone marrow and invades the blood): 9 people, 12.00%
  7. Acute Graft Versus Host Disease (acute complication following an allogeneic tissue/blood transplant): 8 people, 10.67%
  8. Medulloblastoma (a fast-growing, high-grade tumour that always begins in the cerebellum): 4 people, 5.33%

* 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 Thiotepa and Azacitidine:

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 Thiotepa:

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 Azacitidine:

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 Thiotepa 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 Azacitidine 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 thiotepa and azacitidine (the active ingredients of Thiotepa and Azacitidine, respectively), and Thiotepa and Azacitidine (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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