Zaditor and Cellulitis - a phase IV clinical study of FDA data
Summary:
Cellulitis is reported as a side effect among people who take Zaditor (ketotifen fumarate), especially for people who are female, 60+ old, also take Symbicort, and have Immunodeficiency common variable.
The phase IV clinical study analyzes which people have Cellulitis when taking Zaditor. It is created by eHealthMe based on reports of 4,423 people who have side effects when taking Zaditor from the FDA, and is updated regularly.
What is Zaditor?
Zaditor has active ingredients of ketotifen fumarate. It is often used in eye allergy. eHealthMe is studying from 4,448 Zaditor users. Check the latest studies of Zaditor.
What is Cellulitis?
Cellulitis (infection under the skin) is found to be associated with 2,084 drugs and 2,338 conditions by eHealthMe. Check the latest studies of Cellulitis.
4,423 people reported to have side effects when taking Zaditor.
Among them, 11 people (0.25%) have Cellulitis.

Among these 11 people:
What is the gender of people who have Cellulitis when taking Zaditor? *
- female: 100 %
- male: 0.0 %
What is the age of people who have Cellulitis when taking Zaditor? *
- 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: 0.0 %
- 60+: 100 %
What are other drugs people take besides Zaditor? *
- Zyrtec: 11 people, 100.00%
- Singulair: 11 people, 100.00%
- Crestor: 11 people, 100.00%
- Fiorinal: 11 people, 100.00%
- Lexapro: 11 people, 100.00%
- Ondansetron: 11 people, 100.00%
- Proair Hfa: 11 people, 100.00%
- Lyrica: 11 people, 100.00%
- Topamax: 11 people, 100.00%
- Symbicort: 11 people, 100.00%
What are other side effects people have besides Cellulitis? *
- Infusion Site Urticaria (rash of round, red welts on the skin at infusion site): 9 people, 81.82%
- Infusion Site Pruritus (severe itching at infusion site): 9 people, 81.82%
- Infusion Site Erythema (reddening of the skin at infusion site): 8 people, 72.73%
- Seasonal Allergy (allergic condition due to certain season): 8 people, 72.73%
- Thyroid Diseases: 6 people, 54.55%
- Multiple Allergies (allergy to multiple agents): 5 people, 45.45%
- Asthma: 5 people, 45.45%
- Infusion Site Rash: 4 people, 36.36%
- Sneezing: 3 people, 27.27%
- Rhinorrhea (watery mucus discharge from the nose): 3 people, 27.27%
What are the existing conditions these people have? *
- Immunodeficiency Common Variable: 11 people, 100.00%
* Approximation only. Some reports may have incomplete information.
Do you take Zaditor and have Cellulitis?
- Check whether Cellulitis 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 Zaditor:
- Zaditor (4,448 reports)
Cellulitis treatments and more:
- Cellulitis (75,290 reports)
How severe was Cellulitis and when was it recovered:
Expand to all the drugs that have ingredients of ketotifen fumarate:
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 Zaditor:
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 Cellulitis:
- Cellulitis (2,084 drugs)
Browse all the conditions that are associated with Cellulitis:
- Cellulitis (2,338 conditions)
Related publications that referenced our studies
- Yaylaci S, Yilmaz EU, Guclu E, Kumsar NA, Tamer A, Karabay O, "Clozapine-Induced Febrile Neutropenia and Cellulitis", Turkish journal of emergency medicine, 2014 Mar .
- Yaylaci S, Yilmaz EU, Guclu E, Kumsar NA, Tamer A, Karabay O, "Clozapine-Induced Febrile Neutropenia and Cellulitis", Turkish journal of emergency medicine, 2014 Mar .
How the study uses the data?
The study uses data from the FDA. It is based on ketotifen fumarate (the active ingredients of Zaditor) and Zaditor (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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