Medications & Treatments For discussion about medications and treatments for any disease or health condition, including issues of medication toxicity.


advertisement
Reply
 
Thread Tools Display Modes
Old 01-23-2008, 10:50 AM #1
Kristi's Avatar
Kristi Kristi is offline
Member
 
Join Date: Jan 2008
Location: Metro detroit area of Michigan
Posts: 200
15 yr Member
Kristi Kristi is offline
Member
Kristi's Avatar
 
Join Date: Jan 2008
Location: Metro detroit area of Michigan
Posts: 200
15 yr Member
Default Does anyone on Copaxone suffer from Insomnia ?

I've been Copaxone for 3 months and for the last several days,I'm not sleepy at night at all I'm wide awake and I can't figure it out. I've had to resort to taking Tylenol PM at night just to get a good night's sleep I don't want to get addicted to the drug and then feel like I can't go to sleep without it. I also take baclofen but only a small dose 10 mgs at bedtime. Maybe it's stress I don't know I did read the copaxone brochure that comes with my medicine when it's delevered and it say in 2 percent of patients it talks about insomnia and or sleep disorders.And copaxone also causes dry month too,I went to the dentist last week for a check-up and it's not good.I have early peridontal disease at my last check-up most of my teeeth were 2's and now I have 4's and one tooth is a 5 and I need about 6 teeth deep cleaned they have to numb me up and they clean under the gums or something like and it costs alot of money and I have No dental insurance. The hygentist said alot of people with auto-immune diseases suffer from alot of dental problems. I guess it could be stress as I am stressed out about all this. Thanks for listening Kristi.
__________________
Diagnosed Probable MS 9/21/07
.

Started Copaxone 10/16/07


3-6-9 the goose drank wine the monkey chewed tobacoo on the street car line the line broke the monkey got choked and they all went to heaven in a little row boat...
.
Kristi is offline   Reply With QuoteReply With Quote

advertisement
Old 01-29-2008, 12:59 PM #2
MizBarbie's Avatar
MizBarbie MizBarbie is offline
Junior Member
 
Join Date: Jan 2008
Location: Bottom of a Martini Glass
Posts: 49
15 yr Member
MizBarbie MizBarbie is offline
Junior Member
MizBarbie's Avatar
 
Join Date: Jan 2008
Location: Bottom of a Martini Glass
Posts: 49
15 yr Member
Default

Do you take your shot at night? Maybe changing it to morning would help.

I've read elsewhere that it has caused sleep problems for some people. I take other meds that disrupt my sleep pattern, so I take 0.5 mg of Ativan at bedtime. I've been doing that for years.

Hope you work it out.
__________________
Barbie

The woods are lovely, dark, and deep
but I have promises to keep,
and miles to go before I sleep,
and miles to go before I sleep.
--Robert Frost
MizBarbie is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Kristi (01-29-2008)
Old 01-29-2008, 04:20 PM #3
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
Lightbulb some people

react to amino acids this way. It depends on your metabolic status.
Everyone has different ratios of aminos in their systems.

Glutamic acid is a neurostimulant, and may be the culprit.
One remedy for reactions to glutamate in foods, is to use vitamin B6 to offset
reactions.

You might try using a P5P product-- activated B6 and see if that helps.
NOW makes one: One a day of this is plenty.
http://www.iherb.com/ProductDetails.aspx?c=1&pid=740

Stores that have a large NOW section may have it.. but it is reasonable online at iherb.

I do not know enough about MS and vitamins however, to suggest that B6 is helpful or interferes with other MS treatments. So keep that in mind. If you can use B-complex okay, then try that or the more active P5P.
__________________
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
"Thanks for this!" says:
Kristi (01-29-2008)
Old 01-29-2008, 05:50 PM #4
Kristi's Avatar
Kristi Kristi is offline
Member
 
Join Date: Jan 2008
Location: Metro detroit area of Michigan
Posts: 200
15 yr Member
Kristi Kristi is offline
Member
Kristi's Avatar
 
Join Date: Jan 2008
Location: Metro detroit area of Michigan
Posts: 200
15 yr Member
Default

Thanks Miz Barbie, I have though about taking my shots in the morning instead of at night I may try it and see how I feel.


Thanks mrsd, what you said sounds very interesting indeed.

Thanks again Kristi.
__________________
Diagnosed Probable MS 9/21/07
.

Started Copaxone 10/16/07


3-6-9 the goose drank wine the monkey chewed tobacoo on the street car line the line broke the monkey got choked and they all went to heaven in a little row boat...
.
Kristi is offline   Reply With QuoteReply With Quote
Old 01-31-2008, 02:30 PM #5
tovaxin_lab_rat's Avatar
tovaxin_lab_rat tovaxin_lab_rat is offline
Elder
 
Join Date: May 2007
Posts: 7,009
15 yr Member
tovaxin_lab_rat tovaxin_lab_rat is offline
Elder
tovaxin_lab_rat's Avatar
 
Join Date: May 2007
Posts: 7,009
15 yr Member
Default

Kristi

When I was on Copaxone, I took my shot in the morning. I didn't need any more sleep interruptions than I already had. When I first started it, I took my shot at night and had trouble sleeping. I just figured it was the C so changed the shot to morning right after my shower.

I also didn't use the autoinflictor which cut down the site reactions but in the end, I had to quit C because of the severe fatigue that I was experiencing.
__________________
Cheryl
Dx: MS 2001 CRPS 2009




“When everything seems to be going against you, remember that the airplane takes off against the wind, not with it.” - Henry Ford
tovaxin_lab_rat is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Kristi (02-01-2008)
Old 02-01-2008, 05:07 PM #6
Kristi's Avatar
Kristi Kristi is offline
Member
 
Join Date: Jan 2008
Location: Metro detroit area of Michigan
Posts: 200
15 yr Member
Kristi Kristi is offline
Member
Kristi's Avatar
 
Join Date: Jan 2008
Location: Metro detroit area of Michigan
Posts: 200
15 yr Member
Default

Quote:
Originally Posted by Av8rgirl View Post
Kristi

When I was on Copaxone, I took my shot in the morning. I didn't need any more sleep interruptions than I already had. When I first started it, I took my shot at night and had trouble sleeping. I just figured it was the C so changed the shot to morning right after my shower.

I also didn't use the autoinflictor which cut down the site reactions but in the end, I had to quit C because of the severe fatigue that I was experiencing.
Hi,Av8rgirl

I have a question for you so how long were you on Copaxone before your sleep was interrupted see I 've been on C for almost 4 months now and this sleep issue justed started for me about 2 weeks ago out of the blue,I think I'm going to switch to morning shots and try it. See with me I'm not getting tired at night like I should be maybe it's the C or maybe stress heck I dunno. Thanks moderator
__________________
Diagnosed Probable MS 9/21/07
.

Started Copaxone 10/16/07


3-6-9 the goose drank wine the monkey chewed tobacoo on the street car line the line broke the monkey got choked and they all went to heaven in a little row boat...
.
Kristi is offline   Reply With QuoteReply With Quote
Old 02-02-2008, 01:54 AM #7
PolarExpress's Avatar
PolarExpress PolarExpress is offline
Grand Magnate
 
Join Date: Jan 2008
Location: Red Wing, MN
Posts: 3,166
15 yr Member
PolarExpress PolarExpress is offline
Grand Magnate
PolarExpress's Avatar
 
Join Date: Jan 2008
Location: Red Wing, MN
Posts: 3,166
15 yr Member
Default

Honestly, I had the exact opposite reaction. I didn't realize the Copaxone had anything to do with it until I quit. It wasn't the sole cause of my fatigue, but it has improved somewhat since I no longer take it..If it kept me awake, I'd probably still be taking it, whether it helped slow down MS or not..
__________________

.
PolarExpress is offline   Reply With QuoteReply With Quote
Old 02-02-2008, 09:31 AM #8
Kristi's Avatar
Kristi Kristi is offline
Member
 
Join Date: Jan 2008
Location: Metro detroit area of Michigan
Posts: 200
15 yr Member
Kristi Kristi is offline
Member
Kristi's Avatar
 
Join Date: Jan 2008
Location: Metro detroit area of Michigan
Posts: 200
15 yr Member
Default

This morning I did my first morning shot were see what happening I'll give this a month I'll see how I feel at night if there's no change at night within a month and I'm still not getting tired at night then it's probably not the Copaxone and it's something else.
__________________
Diagnosed Probable MS 9/21/07
.

Started Copaxone 10/16/07


3-6-9 the goose drank wine the monkey chewed tobacoo on the street car line the line broke the monkey got choked and they all went to heaven in a little row boat...
.
Kristi is offline   Reply With QuoteReply With Quote
Old 02-02-2008, 12:41 PM #9
Jules A Jules A is offline
Senior Member
 
Join Date: Jan 2008
Posts: 1,424
15 yr Member
Jules A Jules A is offline
Senior Member
 
Join Date: Jan 2008
Posts: 1,424
15 yr Member
Default

I've been on Copaxone for over 3 years now. I do my shots at night and don't have any sleep problems, knock wood!

Good luck figuring it out.
Jules A is offline   Reply With QuoteReply With Quote
Old 02-23-2008, 08:07 PM #10
Victorya Victorya is offline
Member
 
Join Date: Jan 2008
Location: Los Gatos, CA
Posts: 187
15 yr Member
Victorya Victorya is offline
Member
 
Join Date: Jan 2008
Location: Los Gatos, CA
Posts: 187
15 yr Member
Default

Wow...It's funny to be reading this thread. I've been taking Copaxone for about two years (?) and I've been dealing with pretty severe fatigue for the last six months or so.

This time, I'm pretty sure the fatigue has more to due with my nighttime sleep quality than anything else. I've tried switching my copaxone from nite to morning, and even stopped taking the shot for a short time...made no difference.

It gets to the point that I'm so exhausted, but in order to get a good nite's sleep, I have to take about three Tylenol PMs. Of course, the next day I feel slightly hung over...but at least I don't feel tired

It doesn't make sense to be so tired but still not be able to sleep through the night without taking a drug. The weird thing is, I have experimented with smaller doses of Tylenol PM and if I don't take three tablets, I don't sleep through the night. That's more than the dose they recommend, so it's not something I feel I can take often.

I guess it's time to go visit the neuro.
__________________
~Victorya~
------------------------------------------
Spring 2002/present - Double Vision
Feb./Dec. 2004 - Optic Neuritis
Dec. 17,2004 - Diagnosed RRMS
Feb. 9, 2005 - First Rebif injection
Mar. 7, 2006 - "Copaxonator"
------------------------------------------
Victorya is offline   Reply With QuoteReply With Quote
Reply


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
Does anyone on Copaxone suffer from Insomnia ? Kristi Multiple Sclerosis 11 01-24-2008 08:28 AM
Study on double dose Copaxone wannabe Multiple Sclerosis 6 05-07-2007 06:55 PM
Copaxone question greenapple Multiple Sclerosis 8 05-07-2007 04:30 PM
More Good News On Copaxone pantos Multiple Sclerosis 1 10-13-2006 09:32 AM


All times are GMT -5. The time now is 01:55 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.