Rasagaline: Hello, Lately Parkinson has... - Cure Parkinson's

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Rasagaline

Bouffere85 profile image
7 Replies

Hello, Lately Parkinson has been winning on me ! My Doctor today prescribed Rasagaline, I am undecided if I should add it to Sinemete or my other option she said is increase Sinemet.

Any of you take it? any side effects? About the combination with Sinemet? any comments?

Thank you

chantal

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Bouffere85
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johntPM profile image
johntPM

1mg rasagiline gives total symptomatic relief roughly equivalent to about 100mg levodopa (taken with carbidopa). The nice thing about it is that it has an almost level effect over a whole day, whereas levodopa only lasts for about 3 hours. The bad news is that since its benefit is spread across the whole day, its impact at any moment is low. (100mg levodopa over 3 hours = 33mg/hr; 1mg rasagiline over 24 hours = 100/24 = 4mg/hr levodopa equivalent.) For most people the dose is 1mg/day; taking more gives no advantage.

Rasagiline possibly slows down the rate of progression of the disease. There has been much controversy amongst researchers and regulators as to whether this is the case. The latest research suggests that rasagiline may slow progression by 20%.

John

ruff1 profile image
ruff1 in reply tojohntPM

My husband added 1mg to his stelevo a couple of years ago gradually made a difference , very few off periods . No side affects 😀😀

sjannie profile image
sjannie

i have rasagiline 1 mg for about 7 years together with stalevo and neuropatch 4 mg. no side afects

Sane1 profile image
Sane1

I have been on Rasagiline along with Mirapex for about 2 years( since diagnosed). I am donig well with the combo. No noticeable side effects thus far.

cabinfevermt profile image
cabinfevermt

Be very careful. I am on Sinemet, and last year my Neurologist prescribed Rasagiline to complement my Sinemet. The complement soon became an insult. I went into a downward spiral into depression, which eventually led to my attempt to end my life. I have been off of the Rasagiline since October, and life looks a whole lot different now. I can't recall who said this the other day, but I think it is very wise advice; "My advice is to make changes ever so carefully, titrating up or down cautiously. Have very low expectations, and monitor changes closely, caring not to infer quickly any correlation. Managing symptoms and consequences is an art form requiring a very large dose of patients. There is no cure, or panacea for that matter." Be well and take charge of your own health care.

onlysize3feet profile image
onlysize3feet

I was on a sinemet only regime and my neurologist was increasing the dosage every time I went to see them producing some bad side effects. I am now on a medication regime that involves a cocktail of drugs and I'm the best I have ever been. My idea is to try anything that's offered to me and if it doesn't work then try something else also to research to find out if there are any more drugs that might help me and have a discussion about them with my neurologist the next time I see them. Everyone is different.

Bouffere85 profile image
Bouffere85

Thank you all for your responses.

Wish you the best!

Chantal

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