Parkinson's Disease Clinical Trials For posting and discussion of clinical trials related to Parkinson's Disease, and for the Parkinson Pipeline Project. All are welcome.


advertisement
Reply
 
Thread Tools Display Modes
Old 11-06-2013, 10:18 PM #1
debbiehub debbiehub is offline
Member
 
Join Date: Oct 2006
Location: Long Island NY
Posts: 765
15 yr Member
debbiehub debbiehub is offline
Member
 
Join Date: Oct 2006
Location: Long Island NY
Posts: 765
15 yr Member
Default Amantadine

Since I could nt handle sinemet my neuro is giving me amantadine,'any thoughts? I don't know anything about these drugs,
Ty
Debbie
debbiehub is offline   Reply With QuoteReply With Quote

advertisement
Old 11-16-2013, 05:15 AM #2
vlhperry's Avatar
vlhperry vlhperry is offline
Member aka Dianna Wood
 
Join Date: Oct 2006
Posts: 736
15 yr Member
vlhperry vlhperry is offline
Member aka Dianna Wood
vlhperry's Avatar
 
Join Date: Oct 2006
Posts: 736
15 yr Member
Default Hi Deb

Hello Deb,

I was started on Amantadine when originally diagnosed. It was called Eldepral back then (1990) but since I was in denial and didn't know about Sinemet yet
didn't give thought as to if it was the right treatment. Sinemet was added 2 years later. Try posting your question on the members forum. You might get better responce to your question.

Sincerely,
Vicky
vlhperry is offline   Reply With QuoteReply With Quote
Old 11-23-2013, 10:44 AM #3
Owlish's Avatar
Owlish Owlish is offline
Junior Member
 
Join Date: Nov 2013
Location: Northern Virginia, USA
Posts: 15
10 yr Member
Owlish Owlish is offline
Junior Member
Owlish's Avatar
 
Join Date: Nov 2013
Location: Northern Virginia, USA
Posts: 15
10 yr Member
Default medicine

Quote:
Originally Posted by debbiehub View Post
Since I could nt handle sinemet my neuro is giving me amantadine,'any thoughts? I don't know anything about these drugs,
Ty
Debbie
Hi, Debbie,
I haven't taken Amantadine so I can't tell you much about that. I take Carbidopa (Sinemet), Pramipexole, and just started Azilect. I think the medicines are necessary, but so are other tools. What else are you doing for your recovery? I'd be interested in learning new tools and sharing what I know.
Owlish is offline   Reply With QuoteReply With Quote
Old 04-26-2014, 06:11 PM #4
mcolo mcolo is offline
Junior Member
 
Join Date: Apr 2014
Location: Irvine
Posts: 10
8 yr Member
mcolo mcolo is offline
Junior Member
 
Join Date: Apr 2014
Location: Irvine
Posts: 10
8 yr Member
Default Amantadine

Quote:
Originally Posted by debbiehub View Post
Since I could nt handle sinemet my neuro is giving me amantadine,'any thoughts? I don't know anything about these drugs,
Ty
Debbie
I have used it for 5 months and haven't seen much of a difference
mcolo is offline   Reply With QuoteReply With Quote
Old 08-03-2014, 08:34 AM #5
zanpar321 zanpar321 is offline
Member
 
Join Date: Feb 2014
Posts: 365
10 yr Member
zanpar321 zanpar321 is offline
Member
 
Join Date: Feb 2014
Posts: 365
10 yr Member
Default

Quote:
Originally Posted by debbiehub View Post
Since I could nt handle sinemet my neuro is giving me amantadine,'any thoughts? I don't know anything about these drugs,
Ty
Debbie
Amantadine is a weak antagonist of the NMDA type glutamate receptor and is supposed to increase dopamine release. It didn't do anything for me. Hope you have better luck.
zanpar321 is offline   Reply With QuoteReply With Quote
Old 08-03-2014, 10:37 AM #6
mrsD's Avatar
mrsD mrsD is offline
Wisest Elder Ever
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
mrsD mrsD is offline
Wisest Elder Ever
mrsD's Avatar
 
Join Date: Aug 2006
Location: Great Lakes
Posts: 33,508
15 yr Member
Wink

Just a quick reminder here:

Amantadine was branded as Flumadine and
Was the first anti-flu drug long ago.

Eldepryl is selegiline.


Quote:
Originally Posted by vlhperry View Post
Hello Deb,

I was started on Amantadine when originally diagnosed. It was called Eldepral back then (1990) but since I was in denial and didn't know about Sinemet yet
didn't give thought as to if it was the right treatment. Sinemet was added 2 years later. Try posting your question on the members forum. You might get better responce to your question.

Sincerely,
Vicky
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei

************************************

.
Weezie looking at petunias 8.25.2017


****************************
These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
mrsD is offline   Reply With QuoteReply With Quote
Reply

Thread Tools
Display Modes

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
amantadine anon22217 Traumatic Brain Injury and Post Concussion Syndrome 2 05-17-2013 01:56 AM
Amantadine Dolfinwolf Traumatic Brain Injury and Post Concussion Syndrome 1 08-10-2012 07:15 AM
Amantadine Diego24 Parkinson's Disease 0 06-01-2012 11:19 AM
Amantadine and PCS penguinsfan7 Traumatic Brain Injury and Post Concussion Syndrome 1 03-25-2012 05:14 PM
Amantadine indigogo Parkinson's Disease 6 09-07-2006 01:41 PM


All times are GMT -5. The time now is 09:15 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.