Home > Duraprep > Duraprep side effects
Review: Duraprep side effects
In this review, we analyze Duraprep side effects by the time on the drug, gender and age (0-60+) of the people who have side effects while taking Duraprep. The review is based on 121 people who have side effects while taking Duraprep from FDA and social media, and is updated regularly.
What is Duraprep
Duraprep (latest outcomes from 122 users) has active ingredients of iodine povacrylex; isopropyl alcohol. It is often used in preoperative care.
On Aug, 27, 2014: 121 people who reported to have side effects when taking Duraprep are studied
Most common side effects over time * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years||not specified |
|Caustic Injury||n/a||n/a||n/a||n/a||n/a||Headache - Tension||Thermal Burn |
|Excoriation||Application Site Vesicles |
|Application Site Reaction||Pruritus |
|Skin Disorder||Procedural Complication |
|Thermal Burn||Rash |
|Procedural Complication||Erythema |
|Iatrogenic Injury |
|Oedema Peripheral |
Most common side effects by gender * :
|Thermal Burn||Thermal Burn |
|Skin Irritation||Skin Disorder |
|Skin Reaction||Skin Exfoliation |
|Excoriation||Caustic Injury |
|Rash||Application Site Reaction |
|Caustic Injury||Excoriation |
|Pruritus||Skin Irritation |
|Blister||Skin Reaction |
|Skin Disorder||Burns Second Degree |
|Rash Pruritic||Pruritus |
Most common side effects by age * :
|Skin Reaction||n/a||Rash||Thermal Burn||Rash Erythematous||Thermal Burn||Thermal Burn||Thermal Burn |
|Hypersensitivity||Skin Reaction||Blister||Rash Macular||Skin Irritation||Procedural Complication||Burns Second Degree |
|Skin Irritation||Rash Pruritic||Erythema||Impaired Healing||Burns First Degree |
|Thermal Burn||Stevens-johnson Syndrome||Swelling Face||Headache - Tension||Procedural Complication |
|Oedema Genital||Stress||Skin Irritation |
|Thermal Burn||Palpitations|| |
|Rash||Burns Third Degree|| |
|Application Site Vesicles||Maternal Exposure During Delivery|| |
|Skin Irritation||Blood Pressure Increased|| |
* Some reports may have incomplete information.
Browse Duraprep side effects from A to Z:
Comments for this study:
jen schlitz (3 years ago):
I underwent a robotic laproscopic hesterectomy and was told duraprep was used prior to surgery even though I notified the surgeon and the hospital that I had an allergy to topical iodine, bracelet was worn and yet this duraprep was used. I have been dealing with a rash from my breast to mid thigh for two weeks and the pain, itching and blistering are unbearable. Very aggravated!
Reply the comment
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
Are you taking Duraprep?
Comments from related studies:
From this study (3 years ago):
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.
From this study (4 years ago):
Carmen on May, 25, 2010:
I had an iodine CT scan on Saturday night and Sunday I started itching and broke out in a hives type rash by monday...I had alot of tight coughing too, but not trouble breathing or anything else. Is this a reaction to the iodine? It is now Tuesday and the rash is still there although not anywhere near as itchy. Any info would be appreciated...thanks!
More questions for: Duraprep
More reviews for: Duraprep
Studies of common Duraprep drug interactions:
Browse Duraprep drug interactions with drugs from A to Z:
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.