Sutent and Fentanyl-100 drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Sutent (sunitinib malate) and Fentanyl-100 (fentanyl). Common drug interactions include toxic epidermal necrolysis among females and osteonecrosis of jaw among males.

The phase IV clinical study analyzes what interactions people have when they take Sutent and Fentanyl-100. It is created by eHealthMe based on reports of 11 people who take the same drugs from the FDA, and is updated regularly.

What is Sutent?

Sutent has active ingredients of sunitinib malate. It is often used in renal cell carcinoma. eHealthMe is studying from 44,554 Sutent users. Check the latest studies of Sutent.

What is Fentanyl-100?

Fentanyl-100 has active ingredients of fentanyl. It is often used in pain. eHealthMe is studying from 7,047 Fentanyl-100 users. Check the latest studies of Fentanyl-100.



On Jul, 27, 2026

11 people who take Sutent and Fentanyl-100 together, and have interactions are studied.

Sutent and Fentanyl-100 drug interactions.

What are the common drug interactions of Sutent and Fentanyl-100, by gender? *:

female:

  1. Toxic epidermal necrolysis (a rare, life-threatening skin condition that is usually caused by a reaction to drugs causes wide spread skin destruction)

male:

  1. Osteonecrosis of jaw (death of bone of jaw)
  2. Anaemia (lack of blood)
  3. Respiratory failure (inadequate gas exchange by the respiratory system)
  4. Dermatitis contact (skin reaction (dermatitis) resulting from exposure to allergens)
  5. Abdominal pain
  6. Arteriosclerosis (thickening and hardening of arteries)
  7. Cellulitis (infection under the skin)
  8. Gastrointestinal haemorrhage (bleeding gastrointestinal tract)
  9. Haematemesis (vomiting of blood)
  10. Haematochezia (passage of stools containing blood)

What are the common drug interactions of Sutent and Fentanyl-100, by age (0-1 to 60+)? *:

0-1:

n/a

2-9:

n/a

10-19:

n/a

20-29:

  1. Dermatitis contact (skin reaction (dermatitis) resulting from exposure to allergens)
  2. Interstitial lung disease

30-39:

n/a

40-49:

  1. Constipation
  2. Death

50-59:

  1. Bone lesion (bone with abnormalities. bone lesions can result from growth formations, infections, or injuries)
  2. Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body)
  3. Exposed bone in jaw
  4. General physical health deterioration (weak health status)
  5. Jaw fracture
  6. Leukopenia (less number of white blood cells in blood)
  7. Metastases to bone (cancer spreads to bone)
  8. Metastases to lung (cancer spreads to lung)
  9. Neoplasm malignant (cancer tumour)
  10. Neoplasm progression (growth of tumour)

60+:

  1. Abdominal pain
  2. Anxiety
  3. Osteonecrosis of jaw (death of bone of jaw)
  4. Pleural effusion (water on the lungs)
  5. Pulmonary oedema (fluid accumulation in the lungs)
  6. Respiratory failure (inadequate gas exchange by the respiratory system)
  7. Toxic epidermal necrolysis (a rare, life-threatening skin condition that is usually caused by a reaction to drugs causes wide spread skin destruction)
  8. Abdominal discomfort
  9. Actinic keratosis (skin disease due to sun exposure)
  10. Agitation (state of anxiety or nervous excitement)

What are the existing conditions these people have? *

  1. Neoplasm Malignant (cancer tumour): 2 people, 18.18%
  2. Prostate Cancer: 1 person, 9.09%
  3. Pancreatic Neuroendocrine Tumor: 1 person, 9.09%
  4. Nausea And Vomiting: 1 person, 9.09%
  5. Metastatic Renal Cell Carcinoma (spreadable kidney cell tumour): 1 person, 9.09%
  6. Insomnia (sleeplessness): 1 person, 9.09%
  7. Indigestion: 1 person, 9.09%
  8. Gastrointestinal Stromal Tumor: 1 person, 9.09%
  9. Depression: 1 person, 9.09%
  10. Constipation: 1 person, 9.09%

* Approximation only. Some reports may have incomplete information.

Do you take Sutent and Fentanyl-100?

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Related studies:

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

Browse all drug interactions of Sutent and Fentanyl-100:

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 Sutent:

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 Fentanyl-100:

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 Sutent 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 Fentanyl-100 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 sunitinib malate and fentanyl (the active ingredients of Sutent and Fentanyl-100, respectively), and Sutent and Fentanyl-100 (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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