Taxol and Vitiligo - a phase IV clinical study of FDA data
Summary:
Vitiligo is reported as a side effect among people who take Taxol (paclitaxel), especially for people who are female, 50-59 old, have been taking the drug for 1 - 2 years also take Carboplatin, and have High blood pressure.
The phase IV clinical study analyzes which people have Vitiligo when taking Taxol. It is created by eHealthMe based on reports of 33,313 people who have side effects when taking Taxol from the FDA, and is updated regularly.
What is Taxol?
Taxol has active ingredients of paclitaxel. It is often used in breast cancer. eHealthMe is studying from 33,554 Taxol users. Check the latest studies of Taxol.
What is Vitiligo?
Vitiligo (pigment is lost from areas of the skin) is found to be associated with 167 drugs and 306 conditions by eHealthMe. Check the latest studies of Vitiligo.
33,313 people reported to have side effects when taking Taxol.
Among them, 11 people (0.03%) have Vitiligo.

Among these 11 people:
How long have people been on Taxol when they have Vitiligo? *
- < 1 month: 25 %
- 1 - 6 months: 0.0 %
- 6 - 12 months: 0.0 %
- 1 - 2 years: 75 %
- 2 - 5 years: 0.0 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
What is the gender of people who have Vitiligo when taking Taxol? *
- female: 100 %
- male: 0.0 %
What is the age of people who have Vitiligo when taking Taxol? *
- 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 Taxol? *
- Keytruda: 6 people, 54.55%
- Cyclophosphamide: 6 people, 54.55%
- Carboplatin: 6 people, 54.55%
- Promethazine: 3 people, 27.27%
- Palonosetron: 3 people, 27.27%
- Cisplatin: 3 people, 27.27%
- Norvasc: 1 person, 9.09%
- Neulasta: 1 person, 9.09%
- Lorazepam: 1 person, 9.09%
- Lisinopril And Hydrochlorothiazide: 1 person, 9.09%
What are other side effects people have besides Vitiligo? *
- Neuropathy Peripheral (surface nerve damage): 6 people, 54.55%
- Diarrhea: 6 people, 54.55%
- Abdominal Pain: 6 people, 54.55%
- Urticaria (rash of round, red welts on the skin that itch intensely): 1 person, 9.09%
- Tooth Loss: 1 person, 9.09%
- Thrombocytopenia (decrease of platelets in blood): 1 person, 9.09%
- Stomatitis (inflammation of mucous membrane of mouth): 1 person, 9.09%
- Seborrhoeic Dermatitis (a common, inflammatory skin condition that causes flaky, white to yellowish scales to form on oily areas such as the scalp): 1 person, 9.09%
- Hypoaesthesia Facial (reduced sense of touch or sensation on face): 1 person, 9.09%
- Hypoaesthesia (reduced sense of touch or sensation): 1 person, 9.09%
What are the existing conditions these people have? *
- High Blood Pressure: 1 person, 9.09%
* Approximation only. Some reports may have incomplete information.
Do you take Taxol and have Vitiligo?
- Check whether Vitiligo 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 Taxol:
- Taxol (33,554 reports)
Vitiligo treatments and more:
- Vitiligo (3,513 reports)
How severe was Vitiligo and when was it recovered:
Expand to all the drugs that have ingredients of paclitaxel:
- Vitiligo and drugs with ingredients of paclitaxel (19 reports)
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 Taxol:
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 Vitiligo:
- Vitiligo (167 drugs)
Browse all the conditions that are associated with Vitiligo:
- Vitiligo (306 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on paclitaxel (the active ingredients of Taxol) and Taxol (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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