Esbriet and Evista drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Esbriet (pirfenidone) and Evista (raloxifene hydrochloride). Common drug interactions include nausea among females.
The phase IV clinical study analyzes what interactions people have when they take Esbriet and Evista. It is created by eHealthMe based on reports of 13 people who take the same drugs from the FDA, and is updated regularly.
What is Esbriet?
Esbriet has active ingredients of pirfenidone. eHealthMe is studying from 39,858 Esbriet users. Check the latest studies of Esbriet.
What is Evista?
Evista has active ingredients of raloxifene hydrochloride. It is often used in osteoporosis. eHealthMe is studying from 25,891 Evista users. Check the latest studies of Evista.
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 >>>.
13 people who take Esbriet and Evista together, and have interactions are studied.

What are the common drug interactions of Esbriet and Evista, by gender? *:
female:
- Nausea (feeling of having an urge to vomit)
- Decreased appetite
- Sinusitis (inflammation of sinus)
- Abdominal discomfort
- Ephelides (tanned macules found on the skin)
- Hypopnoea (decrease in the breathing rate)
- Insomnia (sleeplessness)
- Oedema (fluid collection in tissue)
- Respiratory disorder (respiratory disease)
- Transient ischaemic attack (a transient episode of neurologic dysfunction caused by ischemia (loss of blood flow))
male:
n/a
What are the common drug interactions of Esbriet and Evista, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
n/a
40-49:
n/a
50-59:
n/a
60+:
- Nausea (feeling of having an urge to vomit)
- Back disorder
- Insomnia (sleeplessness)
- Oedema (fluid collection in tissue)
- Respiratory disorder (respiratory disease)
- Transient ischaemic attack (a transient episode of neurologic dysfunction caused by ischemia (loss of blood flow))
- Abdominal discomfort
- Abdominal pain upper
- Headache (pain in head)
- Shock (a life-threatening condition with symptoms like low blood pressure, weakness, shallow breathing, cold, clammy skin)
What are the existing conditions these people have? *
- Idiopathic Pulmonary Fibrosis (chronic lung disease): 13 people, 100.00%
- Nausea (feeling of having an urge to vomit): 2 people, 15.38%
- High Blood Cholesterol: 2 people, 15.38%
- Stress And Anxiety: 1 person, 7.69%
- Irritable Bowel Syndrome: 1 person, 7.69%
- Hypersensitivity: 1 person, 7.69%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 1 person, 7.69%
- Atrial Fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles): 1 person, 7.69%
* Approximation only. Some reports may have incomplete information.
Do you take Esbriet and Evista?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Esbriet and Evista:
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 zSub-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 Esbriet:
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 side effects of Evista:
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 interactions between Esbriet and drugs from A to Z:
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 interactions between Evista and drugs from A to Z:
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 zHow the study uses the data?
The study uses data from the FDA. It is based on pirfenidone and raloxifene hydrochloride (the active ingredients of Esbriet and Evista, respectively), and Esbriet and Evista (the brand names). 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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