Who have Kerion with Zytiga - from FDA reports


There is no Kerion reported by people who take Zytiga yet. This review analyzes which people have Kerion with Zytiga. It is created by eHealthMe based on reports from FDA, and is updated regularly.

How to use this study: bring a copy to your health teams to ensure drug risks and benefits are fully discussed and understood.


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On Feb, 10, 2019

No report is found.

Do you have Kerion while taking Zytiga?


You are not alone:




Related studies

Zytiga

Zytiga has active ingredients of abiraterone acetate. It is often used in prostate cancer metastatic. (latest outcomes from Zytiga 14,705 users)

Kerion

Kerion (the result of the host's response to a fungal ringworm infection of the hair follicles of the scalp and beard accompanied by secondary bacterial infection(s)) has been reported by people with dermatophytosis, alopecia areata, kerion, rheumatoid arthritis, trichophyton infection (latest reports from 15 Kerion patients).


Drugs that are associated with Kerion
Kerion
Could your condition cause Kerion
Kerion
Zytiga side effects

Browse 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+


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What would happen?

Predict new side effects and undetected conditions when you take Zytiga and have Kerion




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NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.

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, and has not been supported by scientific studies or clinical trials unless otherwise stated. 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.

You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.

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