Melphalan and Sorafenib drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Melphalan (melphalan) and Sorafenib (sorafenib). Common drug interactions include adenoviral hepatitis among females and acute graft versus host disease among males.
The phase IV clinical study analyzes what interactions people have when they take Melphalan and Sorafenib. It is created by eHealthMe based on reports of 30 people who take the same drugs from the FDA, and is updated regularly.
What is Melphalan?
Melphalan has active ingredients of melphalan. eHealthMe is studying from 20,052 Melphalan users. Check the latest studies of Melphalan.
What is Sorafenib?
Sorafenib has active ingredients of sorafenib. eHealthMe is studying from 3,201 Sorafenib users. Check the latest studies of Sorafenib.
30 people who take Melphalan and Sorafenib together, and have interactions are studied.

What are the common drug interactions of Melphalan and Sorafenib, by gender? *:
female:
- Adenoviral hepatitis (viral hepatitis)
- Respiratory failure (inadequate gas exchange by the respiratory system)
- Septic shock (shock due to blood infection)
- Adenovirus infection
- Pneumonia adenoviral (viral pneumonia caused by an adenovirus)
- Leukopenia (less number of white blood cells in blood)
- Tachycardia (a heart rate that exceeds the range of 100 beats/min)
- Pyrexia (fever)
- Hepatitis (inflammation of the liver)
- Pneumonia
male:
- Acute graft versus host disease (acute complication following an allogeneic tissue/blood transplant)
- Alanine aminotransferase increased
- Disseminated intravascular coagulation (systemic activation of blood coagulation)
- Febrile neutropenia (fever with reduced white blood cells)
- Hepatic failure (liver failure)
- Stomatitis (inflammation of mucous membrane of mouth)
- Aspartate aminotransferase increased
- Cardiac failure acute
- Palmar-plantar erythrodysaesthesia syndrome (hand-foot syndrome)
- Pulmonary haemorrhage (acute bleeding from the lung)
What are the common drug interactions of Melphalan and Sorafenib, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
- Acute graft versus host disease (acute complication following an allogeneic tissue/blood transplant)
- Alanine aminotransferase increased
- Aspartate aminotransferase increased
- Cardiac failure acute
- Palmar-plantar erythrodysaesthesia syndrome (hand-foot syndrome)
- Pulmonary haemorrhage (acute bleeding from the lung)
- Renal failure acute (rapid kidney dysfunction)
- Respiratory failure (inadequate gas exchange by the respiratory system)
- Acute myeloid leukaemia recurrent (acute cancer in which the bone marrow makes abnormal myeloblast- recurrent)
- Bone marrow toxicity (decrease in cells responsible for providing immunity, carrying oxygen, and those responsible for normal blood clotting)
10-19:
- Acute graft versus host disease (acute complication following an allogeneic tissue/blood transplant)
- Chronic graft versus host disease (immune cells attack the host's body cells after transplant)
- Cytomegalovirus infection
- Febrile neutropenia (fever with reduced white blood cells)
- Stomatitis (inflammation of mucous membrane of mouth)
20-29:
n/a
30-39:
n/a
40-49:
- Adenoviral hepatitis (viral hepatitis)
- Respiratory failure (inadequate gas exchange by the respiratory system)
- Febrile neutropenia (fever with reduced white blood cells)
- Atypical pneumonia (acute respiratory disease marked by high fever and coughing)
- Coagulopathy (blood's ability to clot is impaired)
- Lung consolidation (a condition whereby the lung tissues solidify because of the accumulation of solid and liquid material in the air spaces)
- Septic shock (shock due to blood infection)
- Adenovirus infection
- Pneumonia adenoviral (viral pneumonia caused by an adenovirus)
- Leukopenia (less number of white blood cells in blood)
50-59:
n/a
60+:
n/a
What are the existing conditions these people have? *
- Acute Myeloid Leukaemia (acute cancer in which the bone marrow makes abnormal myeloblasts): 18 people, 60.00%
- 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): 9 people, 30.00%
- Bone Marrow Conditioning Regimen: 5 people, 16.67%
- Neoplasm Malignant (cancer tumour): 4 people, 13.33%
- Acute Myeloid Leukaemia (In Remission): 2 people, 6.67%
* Approximation only. Some reports may have incomplete information.
Do you take Melphalan and Sorafenib?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Melphalan and Sorafenib:
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 Melphalan:
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 Sorafenib:
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 Melphalan 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 Sorafenib 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 zRelated publications that referenced our studies
- Musri FY, Mutlu H, K?vrak Salim D, Karakurt Ery?lmaz M, ?nal B, Tural D, ?enol Co?kun H, "Sorafenib-induced severe urticaria in a patient with hepatocellular cancer", Journal of Oncology Pharmacy Practice, 2016 Jan .
- Musri FY, Mutlu H, K?vrak Salim D, Karakurt Ery?lmaz M, ?nal B, Tural D, ?enol Co?kun H, "Sorafenib-induced severe urticaria in a patient with hepatocellular cancer", Journal of Oncology Pharmacy Practice, 2016 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on melphalan and sorafenib (the active ingredients of Melphalan and Sorafenib, respectively), and Melphalan and Sorafenib (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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