Prolia and Faecal vomiting - a phase IV clinical study of FDA data

Summary:

Faecal vomiting is reported as a side effect among people who take Prolia (denosumab), especially for people who are female, 50-59 old, also take Sandostatin, and have Gastrointestinal hypomotility.

The phase IV clinical study analyzes which people have Faecal vomiting when taking Prolia. It is created by eHealthMe based on reports of 150,727 people who have side effects when taking Prolia from the FDA, and is updated regularly.

What is Prolia?

Prolia has active ingredients of denosumab. It is often used in osteoporosis. eHealthMe is studying from 151,389 Prolia users. Check the latest studies of Prolia.

What is Faecal vomiting?

Faecal vomiting (faeces in vomiting) is found to be associated with 53 drugs and 358 conditions by eHealthMe. Check the latest studies of Faecal vomiting.

eHealthMe: drug outcomes in the real world

eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.

On Aug, 30, 2026

150,727 people reported to have side effects when taking Prolia.
Among them, 22 people (0.01%) have Faecal vomiting.

Among these 22 people:

What is the gender of people who have Faecal vomiting when taking Prolia? *

female: 100 %
male: 0.0 %

What is the age of people who have Faecal vomiting when taking Prolia? *

What are other drugs people take besides Prolia? *

Sandostatin: 20 people, 90.91%
Vitamin D: 5 people, 22.73%
Codeine: 3 people, 13.64%
Vitamin B12: 2 people, 9.09%
Venlafaxine Hydrochloride: 2 people, 9.09%
Cetirizine Hydrochloride: 2 people, 9.09%
Vitamin D3: 1 person, 4.55%
Probiotic: 1 person, 4.55%
Ondansetron: 1 person, 4.55%
Nexium: 1 person, 4.55%

What are other side effects people have besides Faecal vomiting? *

Nausea (feeling of having an urge to vomit): 22 people, 100.00%
Swallowing Difficulty: 22 people, 100.00%
Weakness: 21 people, 95.45%
Abnormal Faeces (abnormal stool): 21 people, 95.45%
Body Temperature Decreased: 21 people, 95.45%
Bowel Movement Irregularity: 21 people, 95.45%
Diarrhea: 21 people, 95.45%
Flatulence (flatus expelled through the anus): 21 people, 95.45%
Headache (pain in head): 21 people, 95.45%
Injection Site Pain: 21 people, 95.45%

What are the existing conditions these people have? *

Gastrointestinal Hypomotility (less activity of the intestinal tract): 17 people, 77.27%
Primary Intestinal Pseudo-Obstruction (symptoms of intestinal blockage without any physical signs of a blockage): 16 people, 72.73%
Hypersensitivity: 6 people, 27.27%
Short-Bowel Syndrome (a condition in which the body cannot absorb enough fluids and nutrients because part of the small intestine is missing): 1 person, 4.55%

* Approximation only. Some reports may have incomplete information.

Do you take Prolia and have Faecal vomiting?

- Check whether Faecal vomiting is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously

Related studies:

Effectiveness of, long term effects of, and alternative drugs to Prolia:

Prolia (151,389 reports)

Browse all side effects of Prolia:

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 the drugs that are associated with Faecal vomiting:

Faecal vomiting (53 drugs)

Browse all the conditions that are associated with Faecal vomiting:

Faecal vomiting (358 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on denosumab (the active ingredients of Prolia) and Prolia (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.