Is Anyone Taking Rotigotine Patches ? How Are You Getting On With Them And Have You Suffered Any Side Affects .... | MyParkinsonsTeam

Connect with others who understand.

sign up Log in
Resources
About MyParkinsonsTeam
Powered By
Real members of MyParkinsonsTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
Is Anyone Taking Rotigotine Patches ? How Are You Getting On With Them And Have You Suffered Any Side Affects ....
A MyParkinsonsTeam Member asked a question 💭

I am very concerned about the possible side effects that can be suffered by using the above patches x

posted February 8, 2018
View reactions
A MyParkinsonsTeam Member

I started on Rotigotine Neupro patches a couple of months ago. I began with 2mg and slowly increased them to 8mg, but had to drop back to 4mg because the stronger doses made me feel quite nauseous. The only problem I have with them now is skin irritation. Although I move the patch to a different spot every day and avoid using the same place within 14 days, as advised in the instructions, I still have some red, itchy patches that can last for a couple of weeks. Sometimes I have to replace a patch after about 10 hours as I can't stand the itchiness, which of course means that I go through a packet faster than I should.

posted February 11, 2020
A MyParkinsonsTeam Member

I tried patches years ago but they really didn’t work for me !
I later heard from A consultant that the patches should be kept very cold.
I’m not sure if the patches have changed medication format?

posted November 3, 2020
A MyParkinsonsTeam Member

I’ve been on the Neupro patch for a few years and have used the 2, 4, 6, and 8 mg. If I forget to put one on, Its for sure a bad few days for me! I’m using the 4 mg patch now along with taking Rytary capsules. The patch saves me and most of my symptoms, and one of the most annoying is the excessive tremors and sleepless nights. I make sure to put on a patch every day. Luckily, there are no side affects except some itching and I figured out using baby oil on a cotton ball will remove any adhesive marks left around the edges of the patches and rubbing it over the area where the skin where the patch was placed helps the skin. The patch works great for me!

posted July 30, 2020
A MyParkinsonsTeam Member

I use aRotigone patch every dayand take Stalevo. I oftan feel tired but haven't put it down to the patch.

posted February 17, 2018
A MyParkinsonsTeam Member

The printed instructions say not to place the patch in the same place for 14 days. There is a picture on the instructions that shows the silhouette (front, back, and side view) of a body. It has shadowed areas showing where to place the patch. I downloaded a picture similar, shadowed suggested areas, and number each spot on the paper as I apply a patch. That way I am using a different side and different place of the body for 14 days.🙂

posted April 5, 2022

Related content

View All
Has Anyone Taken Neupro ( Rotigotine Transdermal System. Any Bad Side Effects
A MyParkinsonsTeam Member asked a question 💭
I Have Trouble Reading Books & Newspaper Because Of Tremors. Any Suggestions?
A MyParkinsonsTeam Member asked a question 💭
I Have Developed Droop Neck I Do Neck Exercise But Little Improvement I Have Very Short Walking Distance. I Am 77 And Have 13 Years Diagnos
A MyParkinsonsTeam Member asked a question 💭
Continue with Facebook
Continue with Google
Lock Icon Your privacy is our priority. By continuing, you accept our Terms of use, and our Health Data and Privacy policies.
Already a Member? Log in