Ciprofloxacin and Dermatitis atopic aggravated - a phase IV clinical study of FDA data
Summary:
Dermatitis atopic aggravated is reported as a side effect among people who take Ciprofloxacin (ciprofloxacin), especially for people who are male, 40-49 old, also take Dupixent, and have Crohn's disease.
The phase IV clinical study analyzes which people have Dermatitis atopic aggravated when taking Ciprofloxacin. It is created by eHealthMe based on reports of 21,064 people who have side effects when taking Ciprofloxacin from the FDA, and is updated regularly.
What is Ciprofloxacin?
Ciprofloxacin has active ingredients of ciprofloxacin. It is often used in urinary tract infection. eHealthMe is studying from 22,256 Ciprofloxacin users. Check the latest studies of Ciprofloxacin.
What is Dermatitis atopic aggravated?
Dermatitis atopic aggravated (inflammatory, chronically relapsing, non-contagious and pruritic skin disorder) is found to be associated with 612 drugs and 179 conditions by eHealthMe. Check the latest studies of Dermatitis atopic aggravated.
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 >>>.
21,064 people reported to have side effects when taking Ciprofloxacin.
Among them, 18 people (0.09%) have Dermatitis atopic aggravated.

Among these 18 people:
What is the gender of people who have Dermatitis atopic aggravated when taking Ciprofloxacin? *
- female: 44.44 %
- male: 55.56 %
What is the age of people who have Dermatitis atopic aggravated when taking Ciprofloxacin? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 30.77 %
- 20-29: 0.0 %
- 30-39: 15.38 %
- 40-49: 30.77 %
- 50-59: 7.69 %
- 60+: 15.38 %
What are other drugs people take besides Ciprofloxacin? *
- Dupixent: 10 people, 55.56%
- Prednisone: 6 people, 33.33%
- Tacrolimus: 5 people, 27.78%
- Humira: 4 people, 22.22%
- Stelara: 4 people, 22.22%
- Azathioprine: 4 people, 22.22%
- Methotrexate Sodium: 4 people, 22.22%
- Budesonide: 4 people, 22.22%
- Metronidazole: 3 people, 16.67%
- Elidel: 3 people, 16.67%
What are other side effects people have besides Dermatitis atopic aggravated? *
- Rashes (redness): 6 people, 33.33%
- Crohn's Disease (a condition that causes inflammation of the gastrointestinal tract): 4 people, 22.22%
- Skin Disorder (skin disease): 4 people, 22.22%
- Vulvitis (inflammation of the vulva): 4 people, 22.22%
- Episcleritis (acute inflammatory disorder of the episclera of eye): 4 people, 22.22%
- Anal Fistula: 4 people, 22.22%
- Seborrhoeic Dermatitis (a common, inflammatory skin condition that causes flaky, white to yellowish scales to form on oily areas such as the scalp): 4 people, 22.22%
- Itching: 3 people, 16.67%
- Drug Ineffective: 3 people, 16.67%
- Discomfort: 3 people, 16.67%
What are the existing conditions these people have? *
- Vulvitis (inflammation of the vulva): 4 people, 22.22%
- Skin Disorder (skin disease): 4 people, 22.22%
- Crohn's Disease (a condition that causes inflammation of the gastrointestinal tract): 4 people, 22.22%
- Thrombotic Microangiopathy (a pathology that results in thrombosis in capillaries and arterioles, due to an endothelial injury): 2 people, 11.11%
- Eczema (patches of skin become rough and inflamed, with itching and bleeding blisters): 2 people, 11.11%
- Immunoglobulins Decreased: 1 person, 5.56%
- Eye Disorder: 1 person, 5.56%
- Epilepsy (common and diverse set of chronic neurological disorders characterized by seizures): 1 person, 5.56%
- Drug-Induced Liver Injury (diseases of the liver that are caused by physician-prescribed medications): 1 person, 5.56%
- Dermatitis (inflammation of the skin resulting from direct irritation by an external agent or an allergic reaction to it): 1 person, 5.56%
* Approximation only. Some reports may have incomplete information.
Do you take Ciprofloxacin and have Dermatitis atopic aggravated?
- Check whether Dermatitis atopic aggravated 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 Ciprofloxacin:
- Ciprofloxacin (22,256 reports)
Dermatitis atopic aggravated treatments and more:
- Dermatitis atopic aggravated (31 reports)
How severe was Dermatitis atopic aggravated and when was it recovered:
Expand to all the drugs that have ingredients of ciprofloxacin:
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 Ciprofloxacin:
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 Dermatitis atopic aggravated:
- Dermatitis atopic aggravated (612 drugs)
Browse all the conditions that are associated with Dermatitis atopic aggravated:
- Dermatitis atopic aggravated (179 conditions)
Related publications that referenced our studies
- Bolognesi M, Bolognesi D, "Medicine Ciprofloxacin-induced paroxysmal atrial fibrillation", , 2014 Mar .
- Bolognesi M, Bolognesi D, "Ciprofloxacin-induced paroxysmal atrial fibrilation", OA Case Reports, 2012 Jan .
- Bolognesi M, Bolognesi D, "Medicine Ciprofloxacin-induced paroxysmal atrial fibrillation", , 2014 Mar .
- Bolognesi M, Bolognesi D, "Ciprofloxacin-induced paroxysmal atrial fibrilation", OA Case Reports, 2012 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on ciprofloxacin (the active ingredients of Ciprofloxacin) and Ciprofloxacin (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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