Experiences with

Rasagiline

I’m not going to stop taking rasagiline, and I’d rather not start taking Sinemet!

I’m on rasagiline and sometimes mucuna and carbidopa….and should they be discontinued before? If so, how long before? Thanks!

my partner has just been prescribed rasagiline to help with sleep and stiffness she is not on any other medications - done if the side effects look grim - anyone out there tried this?

I am also early stage PD (diagnosed 12/23) and take low dose of levocarbidopa and Rasagiline. I was wondering if this could be PD related? Does anyone else here have this as well as PD? Thank you in advance. I don’t post much but have found this community very helpful. 🙏

I finally had an appointment with the Nurse Practitioner at my MDS office (UCSF), and she suggested a schedule of every four hours - 8am (Rytary), 4x95 plus 1/2 25/100 IR, plus rasagiline 12, 4 pm - one 50/200 CR, and 1/2 25/100 IR.

I want to start medication and would prefer to start with Rasagiline (trying to postpone Levodopa) but doubt if it does anything for dystonia. There is very little resource on this.

I had PD for 5 years, now, have Dystonia and Dyskinesia after took Sinemet, Doctor asks me try Rasagiline, I worry that I take too much med. Dose anyone have experience of Rasagiline？

Hello all, I have been experiencing off times about 3 1/2 hours after taking one C/L, so my MDS suggested one of these three medications as an add on. (I started with Nourianz, which had no effect. I’m wondering about what people’s experiences has been with any of these drugs? Pros and cons? Thanks

I googled it, seems I should stop taking other med include Amantadine and Rasagiline . Does anyone have knowledge and experience of Benzatropine?

I understand that there are complimentary drugs such MAO-B Inhibitors (such as Selegiline, Rasagiline, and Safinamide) I've done some cursory reseach which indicates that MAO-B inhibitors are neuroprotective, may delay alpha-synuclein aggregation and therefore may have disease modifying effects.

I have identified 5 possible reasons for dizziness/lack of balance. 1. decreasing rasagiline too quickly 2. too much carbidopa 3. nOH (neurogenic orthostatic hypotension) Can be caused by rasagilene+rytary) 4. side effect of midodrine (increases when combined with rasagiline) 5.

Hi ! My hwp (77) diagnosed 2017. But of course with hindsight symptoms manifested earlier. Started C/L last year : 25/100 @ 3 times a day. Azilect 1 mg once a day . Walking became a really serious problem a month ago. Partly because of ongoing "sciatica" but also freezing a few times a day. Two weeks

Now the pharmacy says Rasagiline is in short supply in the UK and likely to become unobtainable.

Due to drug shortages we've been unable to get rasagiline and had to swap to selegiline. Since the swap mum has had lots of unusual bleeding and the GP thinks it may be a side effect of the selegiline. Just wondered if anyone else has had similar problems and if so how did you resolve things?.

Victoza)zz GLP-1 (Victoza) GPC L‑alpha‑Glycerylphosphorylcholine (GPC; also known as choline alfoscerate)  L-5-hydroxytryptophan (5-HTP) Kelp Lecithin Licorice Luteolin L-Theanine Lecithin L-Alpha Cysteine Lactoferrin Leucitine Lycopene Magnesium Mannitol MAO-B inhibitors Selegiline, Rasagiline

I have taken Rasagiline for 6 months with no side effects. Neurologist said that it may delay disease progression. Just bought 90 day supply of 1 mg for $100 with GoodRx

I had an appointment with a neurologist who wants me to continue taking Carbidopa-levodopa, but also take Rasagiline. The side effects and food interactions list seem onerous and dangerous to me. And, it is rather expensive. I canceled the prescription until I understand this drug better.

I’m only on rasagiline, B1,

I'm also on Ropinerole 4mg and Rasagiline 1mg. Also I was put on Atorvastatin 20mg two weeks before Madopar and wondered if this pain is caused by them and not Madopar. It's annoying the side effects when you are on a lot of meds.

I’m 2 years into a PD Dx, only on rasagiline and very close to finding my B1 sweet spot, between 100-200 mg. Oral B1. My movement has been improved with B1 after 7 weeks! While going for a ball in pickelball, both my knees just locked, and I fell forward.