Orilissa and Bone loss - a phase IV clinical study of FDA data
Summary:
Bone loss is reported as a side effect among people who take Orilissa (elagolix sodium), especially for people who are female, 30-39 old, have been taking the drug for 1 - 6 months also take Calcium, and have Endometriosis.
The phase IV clinical study analyzes which people have Bone loss when taking Orilissa. It is created by eHealthMe based on reports of 3,300 people who have side effects when taking Orilissa from the FDA, and is updated regularly.
What is Orilissa?
Orilissa has active ingredients of elagolix sodium. eHealthMe is studying from 3,314 Orilissa users. Check the latest studies of Orilissa.
What is Bone loss?
Bone loss is found to be associated with 695 drugs and 559 conditions by eHealthMe. Check the latest studies of Bone loss.
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 >>>.
3,300 people reported to have side effects when taking Orilissa.
Among them, 11 people (0.33%) have Bone loss.

Among these 11 people:
How long have people been on Orilissa when they have Bone loss? *
- < 1 month: 0.0 %
- 1 - 6 months: 50 %
- 6 - 12 months: 25 %
- 1 - 2 years: 25 %
- 2 - 5 years: 0.0 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
What is the gender of people who have Bone loss when taking Orilissa? *
- female: 100 %
- male: 0.0 %
What is the age of people who have Bone loss when taking Orilissa? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 33.33 %
- 30-39: 66.67 %
- 40-49: 0.0 %
- 50-59: 0.0 %
- 60+: 0.0 %
What are other drugs people take besides Orilissa? *
- Vitamin D: 1 person, 9.09%
- Lupron Depot: 1 person, 9.09%
- Lupron: 1 person, 9.09%
- Calcium: 1 person, 9.09%
What are other side effects people have besides Bone loss? *
- Joint Pain: 3 people, 27.27%
- Pain: 3 people, 27.27%
- Osteonecrosis Of Jaw (death of bone of jaw): 2 people, 18.18%
- Adverse Drug Reaction: 2 people, 18.18%
- Mood Swings (an extreme or rapid change in mood): 2 people, 18.18%
- Hot Flush (sudden feelings of heat): 2 people, 18.18%
- Bone Pain: 1 person, 9.09%
- Citric Acid Urine Decreased (low levels of citric acid in urine): 1 person, 9.09%
- Dental Caries: 1 person, 9.09%
- Haemorrhage (bleeding): 1 person, 9.09%
What are the existing conditions these people have? *
- Endometriosis (appearance of endometrial tissue outside the uterus and causing pelvic pain): 9 people, 81.82%
- Stress And Anxiety: 1 person, 9.09%
* Approximation only. Some reports may have incomplete information.
Do you take Orilissa and have Bone loss?
- Check whether Bone loss 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 Orilissa:
- Orilissa (3,314 reports)
Bone loss treatments and more:
- Bone loss (27,142 reports)
How severe was Bone loss and when was it recovered:
Expand to all the drugs that have ingredients of elagolix sodium:
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 Orilissa:
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 Bone loss:
- Bone loss (695 drugs)
Browse all the conditions that are associated with Bone loss:
- Bone loss (559 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on elagolix sodium (the active ingredients of Orilissa) and Orilissa (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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