Amifostine and Mitoxantrone drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Amifostine (amifostine) and Mitoxantrone (mitoxantrone hydrochloride). Common drug interactions include chronic sinusitis among females and acute myeloid leukaemia among males.
The phase IV clinical study analyzes what interactions people have when they take Amifostine and Mitoxantrone. It is created by eHealthMe based on reports of 27 people who take the same drugs from the FDA, and is updated regularly.
What is Amifostine?
Amifostine has active ingredients of amifostine. eHealthMe is studying from 425 Amifostine users. Check the latest studies of Amifostine.
What is Mitoxantrone?
Mitoxantrone has active ingredients of mitoxantrone hydrochloride. eHealthMe is studying from 8,125 Mitoxantrone users. Check the latest studies of Mitoxantrone.
27 people who take Amifostine and Mitoxantrone together, and have interactions are studied.

What are the common drug interactions of Amifostine and Mitoxantrone, by gender? *:
female:
- Chronic sinusitis (long lasting inflammation of the paranasal sinuses)
- Disturbance in attention
- Gallbladder polyp (growths or lesions resembling growths (polypoid lesions) in the wall of the gallbladder)
- Mobility decreased (ability to move is reduced)
- Stomatitis (inflammation of mucous membrane of mouth)
- Surgery
- Tooth extraction
- Wound
- Hypoaesthesia oral (reduced sense of touch or sensation in mouth)
- Dyspnoea (difficult or laboured respiration)
male:
- Acute myeloid leukaemia (acute cancer in which the bone marrow makes abnormal myeloblasts)
- Bleeding time prolonged
- Pneumonia
- Pyrexia (fever)
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Splenomegaly (enlargement of spleen)
- Thrombocytopenia (decrease of platelets in blood)
- Full blood count decreased
- Infection
- Laboratory test abnormal
What are the common drug interactions of Amifostine and Mitoxantrone, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
n/a
40-49:
- Ascites (accumulation of fluid in the abdominal cavity)
- Blood bilirubin increased
- Coma (state of unconsciousness lasting more than six hours)
- Hypoxia (low oxygen in tissues)
- Abdominal distension
- Abdominal pain
- Acute respiratory distress syndrome
- Alanine aminotransferase increased
- Ammonia increased
- Aspartate aminotransferase increased
50-59:
- Chronic sinusitis (long lasting inflammation of the paranasal sinuses)
- Disturbance in attention
- Mobility decreased (ability to move is reduced)
- Stomatitis (inflammation of mucous membrane of mouth)
- Surgery
- Tooth extraction
- Wound
- Gallbladder polyp (growths or lesions resembling growths (polypoid lesions) in the wall of the gallbladder)
- Hypoaesthesia oral (reduced sense of touch or sensation in mouth)
- Migraine (headache)
60+:
- Acute myeloid leukaemia (acute cancer in which the bone marrow makes abnormal myeloblasts)
- Bleeding time prolonged
- Pneumonia
- Pyrexia (fever)
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Splenomegaly (enlargement of spleen)
- Thrombocytopenia (decrease of platelets in blood)
- Full blood count decreased
- Infection
- Laboratory test abnormal
What are the existing conditions these people have? *
- Ovarian Cancer (cancer of ovary): 21 people, 77.78%
- Neoplasm Malignant (cancer tumour): 21 people, 77.78%
- Migraine (headache): 21 people, 77.78%
- Hot Flush (sudden feelings of heat): 21 people, 77.78%
- Discomfort: 21 people, 77.78%
- Breast Cancer Metastatic: 21 people, 77.78%
- Breast Cancer: 21 people, 77.78%
- Granulocyte Count Decreased: 20 people, 74.07%
* Approximation only. Some reports may have incomplete information.
Do you take Amifostine and Mitoxantrone?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
- Amifostine (425 reports)
- Mitoxantrone (8,125 reports)
Browse all drug interactions of Amifostine and Mitoxantrone:
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 zSub-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 Amifostine:
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 zBrowse all side effects of Mitoxantrone:
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 zBrowse all interactions between Amifostine 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 zBrowse all interactions between Mitoxantrone 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 zHow the study uses the data?
The study uses data from the FDA. It is based on amifostine and mitoxantrone hydrochloride (the active ingredients of Amifostine and Mitoxantrone, respectively), and Amifostine and Mitoxantrone (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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