Soliris and Gemcitabine drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Soliris (eculizumab) and Gemcitabine (gemcitabine). Common drug interactions include acute myeloid leukaemia among females and leukopenia among males.
The phase IV clinical study analyzes what interactions people have when they take Soliris and Gemcitabine. 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 Soliris?
Soliris has active ingredients of eculizumab. It is often used in paroxysmal nocturnal hemoglobinuria (pnh). eHealthMe is studying from 58,821 Soliris users. Check the latest studies of Soliris.
What is Gemcitabine?
Gemcitabine has active ingredients of gemcitabine. eHealthMe is studying from 31,337 Gemcitabine users. Check the latest studies of Gemcitabine.
27 people who take Soliris and Gemcitabine together, and have interactions are studied.

What are the common drug interactions of Soliris and Gemcitabine, by gender? *:
female:
- Acute myeloid leukaemia (acute cancer in which the bone marrow makes abnormal myeloblasts)
- Anaemia (lack of blood)
- Headache (pain in head)
- Influenza
- Nausea (feeling of having an urge to vomit)
- Pyrexia (fever)
- Rhinorrhoea (watery mucus discharge from the nose)
- Disease progression
- Pancreatic carcinoma recurrent (pancreatic cancer - recurrent)
- Rash pruritic (redness with itching)
male:
- Leukopenia (less number of white blood cells in blood)
- Carbohydrate antigen 19-9 increased
- Adenocarcinoma (malignant tumour formed from glandular structures in epithelial tissue)
- Cardiac failure congestive
- Haematotoxicity (toxins that destroy red blood cells)
- Ischaemic stroke (stroke; caused by an interruption in the flow of blood to the brain)
- Metastases to bone (cancer spreads to bone)
- Metastases to liver (cancer spreads to liver)
- Metastasis (spreadable cancer to other organ from origin)
- Pancreatic carcinoma (pancreatic cancer)
What are the common drug interactions of Soliris and Gemcitabine, 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:
- Blood lactate dehydrogenase increased
- Haptoglobin decreased
50-59:
- Disease progression
- Carbohydrate antigen 19-9 increased
- General physical health deterioration (weak health status)
- Haemolytic uraemic syndrome (blood clotting disease caused by e. coli infection, birth control pills, pneumonia, medications, and more)
- Hepatic failure (liver failure)
- Pancreatic carcinoma recurrent (pancreatic cancer - recurrent)
- Rash pruritic (redness with itching)
- Thrombotic microangiopathy (a pathology that results in thrombosis in capillaries and arterioles, due to an endothelial injury)
- Adenocarcinoma (malignant tumour formed from glandular structures in epithelial tissue)
- Haematotoxicity (toxins that destroy red blood cells)
60+:
- Acute myeloid leukaemia (acute cancer in which the bone marrow makes abnormal myeloblasts)
- Anaemia (lack of blood)
- General physical health deterioration (weak health status)
- Haemolysis (breaking open of red blood cells and the release of haemoglobin into the surrounding fluid)
- Haemolytic anaemia (anaemia due to haemolysis)
- Infection
- Lung cancer metastatic (lung cancer spreads to other parts)
- Lymphangiosis carcinomatosa (inflammation of the lymph vessels can lead to cancer)
- Renal failure (kidney dysfunction)
- Respiratory distress (difficulty in breathing)
What are the existing conditions these people have? *
- Haemolytic Uraemic Syndrome (blood clotting disease caused by e. coli infection, birth control pills, pneumonia, medications, and more): 14 people, 51.85%
- Thrombotic Microangiopathy (a pathology that results in thrombosis in capillaries and arterioles, due to an endothelial injury): 5 people, 18.52%
- Paroxysmal Nocturnal Haemoglobinuria (haemoglobin in the urine): 5 people, 18.52%
- Neoplasm Malignant (cancer tumour): 3 people, 11.11%
- Breast Cancer: 3 people, 11.11%
- Pancreatic Carcinoma (pancreatic cancer): 2 people, 7.41%
- Non-Small Cell Lung Cancer Stage Iiib: 2 people, 7.41%
- Lung Neoplasm Malignant (cancer tumour of lung): 2 people, 7.41%
* Approximation only. Some reports may have incomplete information.
Do you take Soliris and Gemcitabine?
- 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:
- Soliris (58,821 reports)
- Gemcitabine (31,337 reports)
Browse all drug interactions of Soliris and Gemcitabine:
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 Soliris:
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 Gemcitabine:
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 Soliris 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 Gemcitabine 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
- Alam, S., Illo, C., Ma, Y. T., & Punia, P. , "Gemcitabine-induced cardiotoxicity in patients receiving adjuvant chemotherapy for pancreatic cancer: a case series", Case reports in oncology, 2018 Jan .
- Alam, S., Illo, C., Ma, Y. T., & Punia, P. , "Gemcitabine-induced cardiotoxicity in patients receiving adjuvant chemotherapy for pancreatic cancer: a case series", Case reports in oncology, 2018 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on eculizumab and gemcitabine (the active ingredients of Soliris and Gemcitabine, respectively), and Soliris and Gemcitabine (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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