Atrovent and Fibrin d dimer increased - a phase IV clinical study of FDA data

Summary:

Fibrin d dimer increased is reported as a side effect among people who take Atrovent (ipratropium bromide), especially for people who are female, 40-49 old, also take Albuterol, and have Birth control.

The phase IV clinical study analyzes which people have Fibrin d dimer increased when taking Atrovent. It is created by eHealthMe based on reports of 33,026 people who have side effects when taking Atrovent from the FDA, and is updated regularly.

What is Atrovent?

Atrovent has active ingredients of ipratropium bromide. It is often used in chronic obstructive pulmonary disease. eHealthMe is studying from 33,210 Atrovent users. Check the latest studies of Atrovent.

What is Fibrin d dimer increased?

Fibrin d dimer increased is found to be associated with 518 drugs and 836 conditions by eHealthMe. Check the latest studies of Fibrin d dimer increased.

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

33,026 people reported to have side effects when taking Atrovent.
Among them, 18 people (0.05%) have Fibrin d dimer increased.

Could Atrovent cause Fibrin d dimer increased?

Among these 18 people:

What is the gender of people who have Fibrin d dimer increased when taking Atrovent? *

female: 77.78 %
male: 22.22 %

What is the age of people who have Fibrin d dimer increased when taking Atrovent? *

What are other drugs people take besides Atrovent? *

What are other side effects people have besides Fibrin d dimer increased? *

Chest Pain: 8 people, 44.44%
Atelectasis (partial or complete collapse of the lung): 7 people, 38.89%
Weakness: 6 people, 33.33%
Hypotension (abnormally low blood pressure): 6 people, 33.33%
Thrombocytopenia (decrease of platelets in blood): 5 people, 27.78%
Constipation: 5 people, 27.78%
Pulmonary Embolism (blockage of the main artery of the lung): 5 people, 27.78%
Haemoglobin Decreased: 4 people, 22.22%
Hypokalemia (low potassium): 4 people, 22.22%
Nausea And Vomiting: 4 people, 22.22%

What are the existing conditions these people have? *

Birth Control: 3 people, 16.67%
Multiple Myeloma (cancer of the plasma cells): 2 people, 11.11%
Sepsis (a severe blood infection that can lead to organ failure and death): 1 person, 5.56%
Osteoporosis (bones weak and more likely to break): 1 person, 5.56%
High Blood Pressure: 1 person, 5.56%
Dyspnea (difficult or laboured breathing): 1 person, 5.56%
Chronic Myeloid Leukaemia (long lasting type of cancer that starts in the blood-forming cells of the bone marrow and invades the blood): 1 person, 5.56%
Cardiac Failure Congestive: 1 person, 5.56%

* Approximation only. Some reports may have incomplete information.

Do you take Atrovent and have Fibrin d dimer increased?

- Check whether Fibrin d dimer increased is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
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Related studies:

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

Atrovent (33,210 reports)

Browse all side effects of Atrovent:

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 Fibrin d dimer increased:

Fibrin d dimer increased (518 drugs)

Browse all the conditions that are associated with Fibrin d dimer increased:

Fibrin d dimer increased (836 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on ipratropium bromide (the active ingredients of Atrovent) and Atrovent (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.