Remember Me     Forgot Login?   Sign up   •  Web site Help & Info

!!! DISCUSSION GROUP RULES !!!

1. You must be a registered website user in order to post and comment. Guests may read only.
2. Be kind and helpful, not rude and cynical.
3. Don't advertise or promote anything. You will be banned from the group.
4. Report problems to the moderators. THANK YOU!

Revolade side effects

  • nadeau07@hotmail.com
  • Topic Author
  • Offline
More
14 years 3 weeks ago #23463 by nadeau07@hotmail.com
Revolade side effects was created by nadeau07@hotmail.com
Hi everyone,
I was diagnosed officially with ITP in February. I had two rounds of Prednisone and I had two IVIgs; nothing worked. So now, I am thinking of taking Revolade. I would like to know if someone has tried it and if there were many side effects.
Thank you
Jocelyne

Please Log in or Create an account to join the conversation.

More
14 years 3 weeks ago #23482 by Ann
Replied by Ann on topic Re: Revolade side effects
I haven't taken it so can't help in that way. But it's called Promacta in the US and we tend to call it eltrombopag in the UK. There are several threads about it under those names here so have a read of them and see if they help.

Please Log in or Create an account to join the conversation.

More
14 years 3 weeks ago #23490 by chasty
Replied by chasty on topic Re: Revolade side effects
This is the 2nd week I've been on Promacta and so far the biggest side effect is fatigue.

Please Log in or Create an account to join the conversation.

More
14 years 3 weeks ago #23496 by dmblank
Replied by dmblank on topic Re: Revolade side effects
I just started a new thread with my count but I've been on Promacta for 3 years and have great counts and no side effects. Love it!

Please Log in or Create an account to join the conversation.

  • weirdjack
More
14 years 3 weeks ago #23514 by weirdjack
Replied by weirdjack on topic Re: Revolade side effects
I've taken Promacta for over two years now. It has the least side effects of anything I've used over the past years for treating ITP.
Took awhile to get the dosage right and my count to stabilize on 75mg/day. But after 6 months, I was able to reduce that to 50mg/day and still maintain ≥50k counts. No liver problems, etc.
Side bonus was that it is so stable, I now only need to see my hematologist twice a year.

But, Promacta doesn't work for everyone.
.

Please Log in or Create an account to join the conversation.

You’re not alone. We have answers! Contact PDSA to connect with life altering information, resources and referrals. 440.746.9003 (877.528.3538 toll-free) or PDSA@PDSA.org.

Platelet Disorder Support Association

Platelet Disorder Support Association
8751 Brecksville Road Suite 150
Cleveland, OH 44141
440.746.9003  |  pdsa@pdsa.org
The Platelet Disorder Support Association is a 501(c)3 organization and donations are tax deductible to the fullest extent allowed by law.

IMPORTANT!

The Platelet Disorder Support Association does not provide medical advice or endorse any medication, vitamins or herbs. The information contained herein is not intended nor implied to be a substitute for professional medical advice and is provided for educational purposes only. Always seek the advice of your physician or other qualified healthcare provider before starting any new treatment, discontinuing an existing treatment and to discuss any questions you may have regarding your unique medical condition.