This Is MS Multiple Sclerosis Community: Knowledge & Support

Welcome to the world's leading forum on Multiple Sclerosis research, support, and knowledge. For over 10 years, This is MS has provided an unbiased community dedicated to Multiple Sclerosis patients, caregivers, and affected loved ones.
It is currently Mon Jun 17, 2013 10:51 pm


All times are UTC - 8 hours [ DST ]




Post new topic Reply to topic  [ 6 posts ] 
Author Message
PostPosted: Wed Dec 26, 2012 11:35 pm 
Offline
Newbie

Joined: Wed Dec 26, 2012 11:20 pm
Posts: 2
I have just been on Rebif Since Nov. 21/12 I was on copaxone for 13 years and it was no longer working, witch was to bad as I had no side effects and tolerated it very well, not doing so well with the rebif, went to my full dose last night and today was not very good woke up with major flu like symptoms muscle and joint pain and headache, is this ever going to get any better, it has only been a month but I am getting so discouraged I have always had fatigue with my ms, but this is out of the world fatigue now, if I know it will get better I am sure I can manage to struggle thru it but if not I do not think I can keep taking it, does anyone have any advise or suggestions
thanks Julie


Top
 Profile  
 
PostPosted: Thu Dec 27, 2012 3:45 am 
Offline
Volunteer Moderator
User avatar

Joined: Sat Nov 20, 2004 4:00 pm
Posts: 2761
Hi Julie,
Welcome to ThisIsMS. What are you taking for Rebif's side effects? Many folks find that ibuprofen works fairly well to counteract the side effects from Ifn-B. Since you're on Rebif which is multiple shots every week, I would recommend trying to find the lowest effective dose of ibuprofen that helps. For example, try 200 mg at the time of your shot and then another 200 mg about 4 hours later. Some the next day might also be helpful for getting rid of the lingering aches and mental fog. If 200 mg doesn't work, then up it to 400 mg always being careful not to exceed the recommended dosage. Chronic use of ibuprofen can be problematic so that's why going with the lowest effective dose is best. See if 200 mg makes things more manageable.

NHE


Top
 Profile  
 
PostPosted: Fri Dec 28, 2012 8:32 pm 
Offline
Family Elder
User avatar

Joined: Fri Jun 04, 2004 3:00 pm
Posts: 163
Location: Canada - Ontario - South-West
To add to the above, take the ibuprofen about half an hour BEFORE the shot.

_________________
Carpe Diem


Top
 Profile  
 
PostPosted: Sat Dec 29, 2012 2:56 pm 
Offline
Family Elder
User avatar

Joined: Thu Apr 15, 2010 3:00 pm
Posts: 102
Location: Ohio
Hi Julie,

I was in a similar situation. Started on Copaxone & was on it for nine months. I turned out to be a non-optimal responder as well as suffering from severe hives at the injection site. I've been on Rebif now for almost three years. I can't recall exactly how long it took for my body to adjust, but I had the dreaded flu-like symptoms early on. Several things that may help you out. Staying well hydrated is crucial. Secondly, an earlier injection time may help as well. I was having problems with "wiftiness" and feeling like I were hit by a Mack truck the next day when I did it at night. It sounds counter-intuitive, but an MS Lifelines nurse explained that our metabolism slows down when we sleep and we can't stay hydrated during that time.

As for the Ibuprofen, I wouldn't worry too much about the dosage, save probably taking 800 mg is more than plenty. I take two tabs (400 mg) about an hour before the injection and then an additional tab (200 mg) a 1/2 hour before. It depends on where the injection is. You may also have to take more later on depending on how you feel. If you're concerned about the dosage, you can have your liver enzymes tested with blood work. I have mine done every six months or so and haven't had any problems. Yeah, more needles... Hope you feel better!


Top
 Profile  
 
PostPosted: Sat Feb 02, 2013 10:19 am 
Offline
Newbie
User avatar

Joined: Fri Feb 01, 2013 9:55 am
Posts: 6
Julieg

I shot rebif44 since August/2012, and always wonder, when I go up reactions?
I would answer, but MERCK not have that answer.

I using too Ibuprofeno 600mg and Dipirona Sódica 20mg (50drops).
My sintoms are: Flu, Fever and chills.
I'm here to help you and share my reactions.

By

Leandro

_________________
________________
Leandro Rogério Silva, 34. Married to the best wife who loves me and always motivates me.
Diagnosed July 10, 2012. Rebif44 since August 2012.


Top
 Profile  
 
PostPosted: Tue Feb 05, 2013 10:45 pm 
Offline
Getting to Know You...
User avatar

Joined: Wed Jul 12, 2006 3:00 pm
Posts: 16
Buy the big bottle of Ibu at Costco. My flu like symptoms lasted about 6 months. The reaction was really handy when I was feeling lazy. Been about 6 years since I've been able to use that excuse.


Top
 Profile  
 
Display posts from previous:  Sort by  
Post new topic Reply to topic  [ 6 posts ] 

All times are UTC - 8 hours [ DST ]


Related topics
 Topics   Author   Replies   Views   Last post 
There are no new unread posts for this topic. rebif---

[ Go to pageGo to page: 1, 2, 3 ]

lynn45

32

11778

Wed Oct 20, 2004 8:08 pm

Guest View the latest post

There are no new unread posts for this topic. Getting off of Rebif??

panda

1

3071

Tue May 24, 2005 6:21 am

Trudy View the latest post

There are no new unread posts for this topic. why Rebif?

ga_kristy

2

3284

Tue Oct 18, 2005 4:25 pm

carolsue View the latest post

There are no new unread posts for this topic. Where to buy Rebif?

smoldering

4

3524

Thu Jan 10, 2008 4:14 pm

smoldering View the latest post

There are no new unread posts for this topic. New to Rebif

catfreak

12

3429

Thu Jul 31, 2008 10:06 am

VodooDoll View the latest post

 


Who is online

Users browsing this forum: No registered users


You cannot post new topics in this forum
You cannot reply to topics in this forum
You cannot edit your posts in this forum
You cannot delete your posts in this forum

Search for:
Jump to:  


News News Site map Site map SitemapIndex SitemapIndex RSS Feed RSS Feed Channel list Channel list
Read hundreds of personal Multiple Sclerosis stories on Experience Project. Experience Project is an anonymous community where people connect through their life experiences, made by the same people who built This is MS. With over 30 million personal stories about every possible life experience, you can quickly find people like you!


Interesting: Secret Confessions | Dream Meanings | Ask Questions, Get Answers

Advertise on the premier multiple sclerosis forum