Any experience with Selegilene? - Cure Parkinson's

Cure Parkinson's

25,712 members27,039 posts

Any experience with Selegilene?

Anchor1 profile image
13 Replies

Three years post diagnosis, my neurologist wants me to try Selegilene.

Written by
Anchor1 profile image
Anchor1
To view profiles and participate in discussions please or .
13 Replies
park_bear profile image
park_bear

Helps a bit. No adverse effects experienced.

Zella23 profile image
Zella23

after 4 years on C/L my husband had Rasagaline a similar drug to Selegiline an MAO b inhibitor. It allowed him to keep dopamine drugs at the same level. Still taking it after 9 years.

Recently tapered it down then stopped it for 3 weeks, slowed down quite a bit. Started to slowly retake, it definitely makes a difference to him. But we all react differently to drugs.

Fricnfrac1999 profile image
Fricnfrac1999 in reply to Zella23

Rasagiline did not help my husband. But neither did Entacapone or Opicapone.... Still waiting on that miracle drug .

JH23 profile image
JH23

Just about to start Rasagiline so was going to ask the same question

cjCardio53 profile image
cjCardio53 in reply to JH23

Me, too. (for freezing and poor gait) Let me know how it goes.

MarionP profile image
MarionP

Pretty common, by now, MAO-B inhibitor. Intended to increase and extend the effects of levodopa. Pretty generally well tolerated but like any other drug, you try it and see.

Mandoblast profile image
Mandoblast

S is an earlier version of R. One of its metabolites is Methamphetamine. Doc thought it might give me a boost. I tried Seg in place of Ras for a month. I did feel a bit of a push.. But the constipation was prohibitive. HIs words: " I wonder if you would be one of the patients that do well on Seg...." I guess I wasn't, but still glad he sees the value in trying things.

HugoRipanykhazov profile image
HugoRipanykhazov

I started out on Selegilene and sinemet but stopped the selegilene after a slightly lengthy period 'cos it didnt seem to be doing anything with my very light and very slowly advancing PD. A brain surgeon friend of mine said it was a discredited drug that no one really used much any more.

As I understood it at the time, there had been a suggestion that it could arrest the symptoms of PD.

Ha Ha.

bassofspades profile image
bassofspades

I was on it for a little while. I dont want to get into details, but it was a horrible experience for me.

Farooqji profile image
Farooqji

It worked for me in the beginning of the disease. Still taking it but have not been so effective. It may reinforce levodopa

Farooqji profile image
Farooqji

There was a belief some time ago that selegiline may slow down the progression

PalmSprings profile image
PalmSprings

I have found like some others that it extends the life of the c/l. I stopped taking it for a significant period of time thinking it didn’t do much but then realized that I wasn’t feeling as well. I renewed my prescription and feel it adds to my occasional feeling of wellbeing. But only in conjunction with the c/l because I went the other way with Rasagiline only and I felt virtually no relief.

You may also like...