Gemcitabine and Nexavar drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Gemcitabine (gemcitabine) and Nexavar (sorafenib tosylate). Common drug interactions include abdominal pain upper among females and dyspnoea among males.

The phase IV clinical study analyzes what interactions people have when they take Gemcitabine and Nexavar. It is created by eHealthMe based on reports of 24 people who take the same drugs from the FDA, and is updated regularly.

What is Gemcitabine?

Gemcitabine has active ingredients of gemcitabine. eHealthMe is studying from 31,337 Gemcitabine users. Check the latest studies of Gemcitabine.

What is Nexavar?

Nexavar has active ingredients of sorafenib tosylate. It is often used in hepatocellular carcinoma. eHealthMe is studying from 23,250 Nexavar users. Check the latest studies of Nexavar.



On Jul, 15, 2026

24 people who take Gemcitabine and Nexavar together, and have interactions are studied.

Gemcitabine and Nexavar drug interactions.

What are the common drug interactions of Gemcitabine and Nexavar, by gender? *:

female:

  1. Abdominal pain upper
  2. Fatigue (feeling of tiredness)
  3. Hypertension (high blood pressure)
  4. Cardiac failure
  5. Dyspnoea (difficult or laboured respiration)
  6. Pleural effusion (water on the lungs)
  7. Urinary tract obstruction

male:

  1. Dyspnoea (difficult or laboured respiration)
  2. Diarrhoea
  3. Skin disorder (skin disease)
  4. Skin fibrosis (fibrous tissue formation on skin)
  5. Blood bilirubin increased
  6. Arteriospasm coronary (spasm of the large- or medium-sized coronary arteries)
  7. Ejection fraction decreased (systolic heart failure)
  8. Hepatic neoplasm malignant (liver cancer)
  9. Hypotension (abnormally low blood pressure)
  10. Multi-organ failure (multisystem organ failure)

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

0-1:

n/a

2-9:

  1. Drug ineffective
  2. Hepatoblastoma (liver cancer)
  3. Malignant neoplasm progression (cancer tumour came back)
  4. Terminal state (the transitional states between life and biological death)

10-19:

  1. Urinary tract obstruction

20-29:

n/a

30-39:

n/a

40-49:

n/a

50-59:

  1. Anxiety
  2. Arteriospasm coronary (spasm of the large- or medium-sized coronary arteries)
  3. Arthropathy
  4. Cardiac disorder
  5. Dyspnoea (difficult or laboured respiration)
  6. Ejection fraction decreased (systolic heart failure)
  7. Hepatic neoplasm malignant (liver cancer)
  8. Hypotension (abnormally low blood pressure)
  9. Mobility decreased (ability to move is reduced)
  10. Multi-organ failure (multisystem organ failure)

60+:

  1. Diarrhoea
  2. Fatigue (feeling of tiredness)
  3. Dysphonia (speech disorder attributable to a disorder of phonation)
  4. Hospitalisation
  5. Hypersomnia (excessive daytime sleepiness (eds))
  6. Hypertension (high blood pressure)
  7. Impaired work ability
  8. Jaundice (a yellowish pigmentation of the skin, the conjunctival membranes)
  9. Palmar-plantar erythrodysaesthesia syndrome (hand-foot syndrome)
  10. Pyrexia (fever)

What are the existing conditions these people have? *

  1. Pain: 5 people, 20.83%
  2. High Blood Pressure: 5 people, 20.83%
  3. Hepatic Neoplasm Malignant (liver cancer): 5 people, 20.83%
  4. Tumor: 4 people, 16.67%
  5. Stress And Anxiety: 4 people, 16.67%
  6. Pancreatic Carcinoma (pancreatic cancer): 4 people, 16.67%
  7. Neoplasm Malignant (cancer tumour): 4 people, 16.67%
  8. Constipation: 4 people, 16.67%
  9. Type 2 Diabetes: 3 people, 12.50%
  10. Renal Cell Carcinoma Stage Unspecified (kidney cancer in unknown stage): 2 people, 8.33%

* Approximation only. Some reports may have incomplete information.

Do you take Gemcitabine and Nexavar?

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Related studies:

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

Browse all drug interactions of Gemcitabine and Nexavar:

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 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 z

Browse all side effects of Nexavar:

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 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 z

Browse all interactions between Nexavar 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

Related publications that referenced our studies


How the study uses the data?

The study uses data from the FDA. It is based on gemcitabine and sorafenib tosylate (the active ingredients of Gemcitabine and Nexavar, respectively), and Gemcitabine and Nexavar (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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