Ventavis and Hip fracture - a phase IV clinical study of FDA data

Summary:

Hip fracture is reported as a side effect among people who take Ventavis (iloprost), especially for people who are female, 60+ old, have been taking the drug for 6 - 12 months also take Tracleer, and have Primary pulmonary hypertension.

The phase IV clinical study analyzes which people have Hip fracture when taking Ventavis. It is created by eHealthMe based on reports of 11,968 people who have side effects when taking Ventavis from the FDA, and is updated regularly.

What is Ventavis?

Ventavis has active ingredients of iloprost. eHealthMe is studying from 11,982 Ventavis users. Check the latest studies of Ventavis.

What is Hip fracture?

Hip fracture is found to be associated with 1,325 drugs and 1,087 conditions by eHealthMe. Check the latest studies of Hip fracture.

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, 27, 2026

11,968 people reported to have side effects when taking Ventavis.
Among them, 48 people (0.4%) have Hip fracture.

$Could Ventavis cause Hip fracture?$

Among these 48 people:

How long have people been on Ventavis when they have Hip fracture? *

What is the gender of people who have Hip fracture when taking Ventavis? *

female: 84.38 %
male: 15.62 %

What is the age of people who have Hip fracture when taking Ventavis? *

What are other drugs people take besides Ventavis? *

What are other side effects people have besides Hip fracture? *

Fall: 32 people, 66.67%
Death: 8 people, 16.67%
Pneumonia: 7 people, 14.58%
Head Injury: 7 people, 14.58%
Dizziness: 7 people, 14.58%
Dyspnea (difficult or laboured breathing): 6 people, 12.50%
Hypotension (abnormally low blood pressure): 5 people, 10.42%
Cardiac Arrest: 5 people, 10.42%
Oedema Peripheral (superficial swelling): 5 people, 10.42%
Fainting (loss of consciousness and postural tone): 4 people, 8.33%

What are the existing conditions these people have? *

Primary Pulmonary Hypertension (primary high blood pressure that affects the arteries in the lungs and the right side of your heart): 39 people, 81.25%
Pulmonary Hypertension (increase in blood pressure in the lung artery): 5 people, 10.42%
Respiratory Distress (difficulty in breathing): 2 people, 4.17%
Pain: 2 people, 4.17%
Osteopenia (a condition where bone mineral density is lower than normal): 1 person, 2.08%
Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 1 person, 2.08%
Cor Pulmonale Chronic (long lasting enlargement of the right ventricle of the heart): 1 person, 2.08%

* Approximation only. Some reports may have incomplete information.

Do you take Ventavis and have Hip fracture?

- Check whether Hip fracture 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 Ventavis:

Ventavis (11,982 reports)

Hip fracture treatments and more:

Hip fracture (39,233 reports)

Browse all side effects of Ventavis:

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 Hip fracture:

Hip fracture (1,325 drugs)

Browse all the conditions that are associated with Hip fracture:

Hip fracture (1,087 conditions)

How the study uses the data?

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