Femara and Acarodermatitis - a phase IV clinical study of FDA data
Summary:
Acarodermatitis is reported as a side effect among people who take Femara (letrozole), especially for people who are female, 50-59 old, also take Kisqali, and have Gastritis.
The phase IV clinical study analyzes which people have Acarodermatitis when taking Femara. It is created by eHealthMe based on reports of 19,093 people who have side effects when taking Femara from the FDA, and is updated regularly.
What is Femara?
Femara has active ingredients of letrozole. It is often used in breast cancer. eHealthMe is studying from 19,630 Femara users. Check the latest studies of Femara.
What is Acarodermatitis?
Acarodermatitis (skin inflammation caused by mites (acarids)) is found to be associated with 208 drugs and 311 conditions by eHealthMe. Check the latest studies of Acarodermatitis.
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 >>>.
19,093 people reported to have side effects when taking Femara.
Among them, 14 people (0.07%) have Acarodermatitis.

Among these 14 people:
What is the gender of people who have Acarodermatitis when taking Femara? *
- female: 100 %
- male: 0.0 %
What is the age of people who have Acarodermatitis when taking Femara? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 100 %
- 60+: 0.0 %
What are other drugs people take besides Femara? *
- Kisqali: 14 people, 100.00%
- Zoledronic Acid: 11 people, 78.57%
- Vitamin D3: 11 people, 78.57%
- Thiamine: 11 people, 78.57%
- Omeprazole: 11 people, 78.57%
- Folic Acid: 11 people, 78.57%
- Calcium Carbonate: 11 people, 78.57%
- Calcium: 11 people, 78.57%
- Hydrocodone: 7 people, 50.00%
- Letrozole: 1 person, 7.14%
What are other side effects people have besides Acarodermatitis? *
- White Blood Cell Count Decreased: 14 people, 100.00%
- Rashes (redness): 14 people, 100.00%
- Elbow Deformity: 14 people, 100.00%
- Eye Disorder: 14 people, 100.00%
- Pain: 14 people, 100.00%
- Eye Swelling: 14 people, 100.00%
- Fever: 14 people, 100.00%
- Haemoglobin Decreased: 14 people, 100.00%
- Haemorrhoids (a swollen vein or group of veins in the region of the anus): 14 people, 100.00%
- Headache (pain in head): 14 people, 100.00%
What are the existing conditions these people have? *
- Gastritis (inflammation of stomach): 11 people, 78.57%
- Breast Cancer Metastatic: 3 people, 21.43%
- Pain: 1 person, 7.14%
* Approximation only. Some reports may have incomplete information.
Do you take Femara and have Acarodermatitis?
- Check whether Acarodermatitis 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 Femara:
- Femara (19,630 reports)
Acarodermatitis treatments and more:
- Acarodermatitis (2,497 reports)
How severe was Acarodermatitis and when was it recovered:
Expand to all the drugs that have ingredients of letrozole:
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 Femara:
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 Acarodermatitis:
- Acarodermatitis (208 drugs)
Browse all the conditions that are associated with Acarodermatitis:
- Acarodermatitis (311 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on letrozole (the active ingredients of Femara) and Femara (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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