Subsys and Cachexia - a phase IV clinical study of FDA data
Summary:
Cachexia is reported only by a few people who take Subsys.
The study analyzes which people take Subsys and have Cachexia. It is created by eHealthMe based on reports of 9,232 people who have side effects while taking Subsys from the FDA, and is updated regularly.
What is Subsys?
Subsys has active ingredients of fentanyl. eHealthMe is studying from 9,239 Subsys users. Check the latest studies of Subsys.
What is Cachexia?
Cachexia (loss of weight) is found to be associated with 710 drugs and 1,194 conditions by eHealthMe. Check the latest studies of Cachexia.
9,232 people reported to have side effects when taking Subsys.
Among them, 3 people (0.03%) have Cachexia.

Among these 3 people:
How long have people been on Subsys when they have Cachexia? *
- < 1 month: 100 %
- 1 - 6 months: 0.0 %
- 6 - 12 months: 0.0 %
- 1 - 2 years: 0.0 %
- 2 - 5 years: 0.0 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
What is the gender of people who have Cachexia when taking Subsys? *
- female: 100 %
- male: 0.0 %
What is the age of people who have Cachexia when taking Subsys? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 100 %
- 40-49: 0.0 %
- 50-59: 0.0 %
- 60+: 0.0 %
What are other drugs people take besides Subsys? *
- Xanax: 3 people, 100.00%
- Wellbutrin: 3 people, 100.00%
- Valium: 3 people, 100.00%
- Toradol: 3 people, 100.00%
- Medrol: 3 people, 100.00%
- Dilaudid: 3 people, 100.00%
- Decadron: 3 people, 100.00%
- Belsomra: 3 people, 100.00%
- Ativan: 3 people, 100.00%
- Adderall: 3 people, 100.00%
What are other side effects people have besides Cachexia? *
- Weight Decreased: 3 people, 100.00%
- Swelling Face: 3 people, 100.00%
- Suicidal Ideation: 3 people, 100.00%
- Photophobia (extreme sensitivity to light): 3 people, 100.00%
- Paraesthesia (sensation of tingling, tickling, prickling, pricking, or burning of a person's skin with no apparent long-term physical effect): 3 people, 100.00%
- Paleness (unusual lightness of skin colour): 3 people, 100.00%
- Overdose: 3 people, 100.00%
- Nausea (feeling of having an urge to vomit): 3 people, 100.00%
- Interleukin Level Increased: 3 people, 100.00%
- Fatigue (feeling of tiredness): 3 people, 100.00%
What are the existing conditions these people have? *
- Pain: 3 people, 100.00%
- Fibromyalgia (a long-term condition which causes pain all over the body): 3 people, 100.00%
- Complex Regional Pain Syndrome (long lasting pain condition most often affecting one of the limbs (arms, legs, hands, or feet)): 3 people, 100.00%
* Approximation only. Some reports may have incomplete information.
Do you take Subsys and have Cachexia?
- Check whether Cachexia is associated with a drug or a condition (FREE)
- Predict drug outcomes for up to one year with AI (FREE)
- Get an AI agent to monitor your drugs continuously (FREE)
Related studies:
Effectiveness of, long term effects of, and alternative drugs to Subsys:
- Subsys (9,239 reports)
Cachexia treatments and more:
- Cachexia (7,763 reports)
How severe was Cachexia and when was it recovered:
Expand to all the drugs that have ingredients of fentanyl:
- Cachexia and drugs with ingredients of fentanyl (177 reports)
Sub-studies by age:
0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+
Browse all side effects of Subsys:
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 the drugs that are associated with Cachexia:
- Cachexia (710 drugs)
Browse all the conditions that are associated with Cachexia:
- Cachexia (1,194 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on fentanyl (the active ingredients of Subsys) and Subsys (the brand name). 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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