Neupro Patch: Here in the US I believe that... - Cure Parkinson's

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Neupro Patch

Brooke profile image
13 Replies

Here in the US I believe that they have approved use of the Neupro Patch. Can anyone tell me if is worth trying. I was planning on asking my Dr, to prescribe it.

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Brooke profile image
Brooke
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13 Replies
shasha profile image
shasha

i was on it for about 3/4 months and found it ti be useless as well as being very annoying to use

lmacquinn profile image
lmacquinn

I used it about 5 years ago, before it was recalled. It is worth trying.

soniadakini profile image
soniadakini

I am on neupro 10mg a day and have found them very good. They are the only medication that don't give other side effects,

I have been on them for over a year increasing the dose very slowly.

Soniadakini

Brooke profile image
Brooke in reply tosoniadakini

Thank you very much.......Blessings/ I plan to try it.

cabbagecottage profile image
cabbagecottage

My husband is on it now 6mg . Seems to be the one thing that suits him best he also takes Sinemet which I am beginning to think is making him worse . I found the patch helped his mental reasonling

Brooke profile image
Brooke in reply tocabbagecottage

Thank you Cabbagecottage I hope to try it.

Kadie57 profile image
Kadie57

I have good going with mine says taking pils, mine is a 6 mg good for 24 hrs, takes a while to settle in or acutally work well. I have adhesive problems and have had no problems with this patch. it is worth a try if it saves taking pills.

Hikoi profile image
Hikoi

Brooke

The patch is a dopamine agonist similar to ropinerole and with the same potential side effects, drowsiness and sleep attacks, low BP, addictive behaviour etc. In early PD may be given alone then after a time usually with sinemet (L Dopa). It is a good medication for many people. Hope it works well for you.

bleu22 profile image
bleu22 in reply toHikoi

My husband has been on patch for years and has sleep attacks he insists are not happening , in addition to all the other dopamine agonist side effects (compulsions, no sleeping at night, manic mood swings, constant talking in circles about same thing, hostility, misperception and anger)

He loves this drug, because he believes it stops his tremor, I think delusion plays a factor in that. Dr thinks he is doing great.

Recently he totaled car falling asleep at wheel, He is lucky he didn't kill anyone.

Beware

sjannie profile image
sjannie

iam on the neupro patches for about 3 years. i started with 2mg and slowly went up to 12 mg. i am very happy with it and iam doing well without side efects!! wish you the best!!

cabbagecottage profile image
cabbagecottage

My husband has very sensitive skin and occasionally the patch will catch as it's removed but I just cleanse and put some suda creme on it NO problem

.

export profile image
export

I am on 12mg was on 16mg . I told my neuro iI wanted to stop them. In the day time kept falling asleep. Night time couldn't sleep.

PROBLEMS with Neupro they don't stick very well .they only work on my belly. No way do they last 24 hours. Weight increase ,can't stop sweating , skin rash.

yours EXPORT

rory3028 profile image
rory3028

Has anybody had problems with Amantadine? Mine interacted with Reclast, the once-a-year osteoporosis medication, and gave me hallucinations, two years in a row. We weren't sure that was it after the first year, so we took a chance the second year and it happened again.. It was terrible, you feel as if you've lost your mind. Also, my potassium was low and I've been told that contributed to it. I'm on a potassium supplement now, and everythng has cleared up. The hallucinations were terrible, because I knew rhey weren't real, yet I was seeing them right before my eyes. Talk about confusion!!! In addition to the Amantadine, my other Parkinson's meds are Mirapex and Sinemet.

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