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Review: could Duraprep cause Rash vesicular?

Summary: there is no Rash vesicular reported by people who take Duraprep yet.

We study 121 people who have side effects while taking Duraprep from FDA and social media. Find out below who they are, when they have Rash vesicular and more.

You are not alone: join a mobile support group for people who take Duraprep and have Rash vesicular >>>


Duraprep has active ingredients of iodine povacrylex; isopropyl alcohol. It is often used in preoperative care. (latest outcomes from Duraprep 122 users)

Rash vesicular

Rash vesicular (rash with a small bubble) has been reported by people with rheumatoid arthritis, pain, high blood pressure, bipolar disorder, depression.(latest reports from Rash vesicular 1,618 patients)

On Dec, 19, 2014: No report is found

Do you have Rash Vesicular while taking Duraprep?

You are not alone! Join a mobile support group:
- support group for people who take Duraprep
- support group for people who have Rash Vesicular

Drugs in real world that are associated with:

Could your condition cause:

More questions for: Duraprep, Rash vesicular

More reviews for: Duraprep, Rash vesicular

Recent related drug studies (Check your drugs):

  • A study of side effects of Duraprep for a patient with Meningioma Surgery. The patient has Thermal Burn (burn by heat)
    Comments: My son had meniscus surgery. Two days post-op, his surgical site was red. After 3 days, blisters developed. The blisters got worse over the following week and my son experienced severe pain. He is now 6 weeks post-op and his skin is scarred.

More related studies for: Duraprep, Rash vesicular

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 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 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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