Experiences with

Entacapone

entacapone?

https://scitechdaily.com/new-study-uncovers-a-shocking-side-effect-of-a-parkinsons-drug/

I was diagnosed with PD since 4 years and I take Mucuna capsules, Carbidopa Levodopa 4x daily and my neurologist recently added Entacapone to my regimen but nothing has helped this nasty symptom. Any suggestions will be appreciated. Maddie

Standard Medical Treatment Glycopyrrolate 1 mg 3 times a day Carbidopa/levodopa 25-100mg 2 tablets three times daily ENTACAPONE 200 MG 1 tablet Orally three times a day 90 days Supplements/Additional Therapy He is trying the following supplements and therapy below.

Hi, I was prescribed Opicapone to extend my 'on' time after trying Entacapone which had made me nauseous and unable to eat. The Opicapone seemed to be a better candidate because of only needing to take it once, at bedtime, 10pm for me, rather than with every Madapar dose .

Entacapone introduced in February. Transferred to Stalevo over a period of four weeks, been on "all Stalevo" for about 5 days. Which, coincidentally (or perhaps not) is the same length of time I've been getting a tingling sensation confined to the tip of my penis (sorry ladies).

My Neuro Doctor prescribed ENTACAPONE 200mg for me. But, other doctor said that will causes my Dyskinesia worse. Besides, I don’t want to take too many med every day. Has anyone ever taken this med? How does it work? Any bad side effect?

I’ve been taking Entacapone for exactly three months because of wearing off times about 45 minutes prior to next Sinemet dose. It has provided a modest improvement in my overall functioning. I’ve been taking it three times per day with 25/100 c/l.

I have seen Entacapone and Amantadine mentioned but don’t know much about them so will try and discuss these too.

Has anybody tried both Entacapone and Opicapone, and which one do you prefer and why? Thank you in advance for the patience to read the above and for any comments you might have.

He is off to the Dr this week and will ask to trial entacapone to see if it smooths things out and he can space the dose timing out more and reduce the dose.

This is a link to info about this drug on the Parkinson's UK website https://www.parkinsons.org.uk/information-and-support/comt-inhibitors-entacapone-opicapone

I now take a pile of CD/LD every 3 hours, but it lasts 2-1/2 hours but I have been taking a new prescription of Entacapone ( 5 x 200 mg per day ) which does extend the time however it seems to cause me to see things that clearly are not there ( looking up the name ).

I'm on carbidopa/levodopa, entacapone and amantadine (100 mg 3x/day). Do you find it causes swelling in the feet, lower legs and hands? If you came off the drug, what was the upside and the downside? How did you come off of it? I understand that you can't quit it abruptly. Thanks for reponses

My consultant has also perscribed Entacapone 200 4 times daily to try and control the tremors.

Two months ago I stopped taking Entacapone, and again, I couldn’t tell any difference. I ran into opicapone, a.k.a. Ongentys, and it seemed to sound like a better option than Entacapone, so I ordered a three month supply of it.

It is not known if treatment with entacapone affects the risk of having prostate cancer. Therefore, it is important for men to have their regular prostate examinations during treatment with entacapone.

The entacapone helps the mucuna be utilised better. 11am. 1. madopar 50/12.5 + NOW dopa mucuna + 1/2 entacapone 2am. 1 madopar 50/12.5 + NOW dopa mucuna + 1/2 entacapone 5am. 1 madopar 50/12.5 8pm 1/2 madopar 50/12.5 this spreads the levodopa over the beginning of the day then reduces

derived neurotropic factor (BDNF) Borage Black Seed Oil (Nigella Saliva) BMPS/7 Broccholi Spores Butyric acid B-carotene Cannabis Cacao Cats Claw CBD Celastrol Celebrex Choline Cinnamon, Ceylon caffeine Coconut Oil Citicholine Citraline CoEnzyme Q10 Collagen COMT inhibitors (entacapone

I decided against entacapone because I already take a few meds that are mildly anticholinergic and I don't want to add to that list. I'd like to hear from those who have successfully switched to Rytary, what to expect from the transition? Any tips?