Home         Forums  

Go Back   Marrowforums > Practical Issues > Questions and Answers
Register FAQ Search Today's Posts Mark Forums Read

Questions and Answers Not sure where to post a question? Post it here.

Reply
 
Thread Tools Search this Thread
  #1  
Old Sat Nov 19, 2016, 07:47 AM
Lennyr Lennyr is offline
Member
 
Join Date: Nov 2016
Location: Somerset new jersey
Posts: 7
Amicar for low platelets

My husband is diagnosed with raeb2. He has blasts of14% and his platelets count is below 10. His doctors have put him on amicar 500mg 6 pills three times a day. Does anyone have any experience with taking this drug? Also it is extremely expensive . Can anyone share how to get financial assistance with this drug?
Reply With Quote
  #2  
Old Sat Nov 19, 2016, 10:14 AM
Margaret W Margaret W is offline
Member
 
Join Date: Dec 2015
Location: Michigan
Posts: 31
I certainly have experience with Amicar. It worked extremely well for me in many circumstances (I have aplastic anemia with a platelet count that, over the years, has been between 0 and about 30,000 usually). I can have no more platelet transfusions because, after 44 years, I've developed antibodies that prohibit my taking further blood products.

I was told about six months ago that Amicar would no longer be available to me. At first, I was told that "the drug is no longer being manufactured," and then I was told that no drug coverage would be available to me for Amicar and I'd have to pay for it out of my own pocket. (I'm on a Medicare Advantage plan through my husband's retirement benefits. I figure that as someone over 65, I'm being "phased out" myself.) Finally, I was told at the University of Michigan that no one would give me a prescription for it and, despite its fine success for me in the past with hemorrhaging problems, it would no longer be provided to me by any means.

Amicar caused no side effects for me, which was unusual because most drugs do, or I have allergies to them. Amicar worked well in stopping stopping spontaneous hemorrhaging and healing petechiae. Its unavailability to me is pretty distressing.

I wish your husband very well with this fine drug. I'm sorry it's so expensive for you - but at least it's available to him. Amicar (aminocaproic acid) helped me a lot!

Margaret
__________________
Margaret, SAA patient diagnosed 1972; ATG 1987; moderate AA for years; hep. C from transfusion 1987; now SAA is back.
Reply With Quote
  #3  
Old Sat Nov 19, 2016, 02:31 PM
bailie bailie is offline
Member
 
Join Date: Dec 2013
Location: McMinnville,OR
Posts: 825
Lennyr, unfortunately many of these drugs come down to insurance. What is your situation? I was also diagnosed with RAEB-II.
__________________
age 70, dx RAEB-2 on 11-26-2013 w/11% blasts. 8 cycles Vidaza 3w/Revlimid. SCT 8/15/2014, relapsed@Day+210 (AML). Now(SCT-Day+1005). Prepping w/ 10 days Dacogen for DLI on 6/9/2017.

Last edited by bailie : Sat Nov 19, 2016 at 05:08 PM.
Reply With Quote
  #4  
Old Sat Nov 19, 2016, 04:37 PM
Lennyr Lennyr is offline
Member
 
Join Date: Nov 2016
Location: Somerset new jersey
Posts: 7
Thank you for your information re amicar

Margaret And Ballie - We have Medicare and united heathcare aarp coverage. They do still make the drug in 500 mg tablets. By the way we just joined so I'm learning the ropes regarding numbers and symbolic letters in reporting blood levels and disease types. I can see already how helpful this site is. My husband is 75. Vidaza did not raise his platelet count . He had a trial on promacta and did not tolerate it well. We are currently waiting to see if he qualifies for a trial on atra at Colombia Presbyterian hospital in New York. He has had red blood cell transfusions and platelet transfusions. Thanks again for your responses
Reply With Quote
  #5  
Old Sun Nov 20, 2016, 01:36 AM
Margaret W Margaret W is offline
Member
 
Join Date: Dec 2015
Location: Michigan
Posts: 31
Well, maybe Amicar is in short supply or something and they only give prescriptions for it in the event that a person is diagnosed with RAEB.

That's fine, of course! I'm happy someone is getting it! I know it's expensive... But so is Promacta. I was told that Promacta would cost me $10,200 out of my own pocket for the first 25 days of treatment, with a 30% chance of doing me any good.

I'm about to book out of the University of Michigan.
__________________
Margaret, SAA patient diagnosed 1972; ATG 1987; moderate AA for years; hep. C from transfusion 1987; now SAA is back.
Reply With Quote
Reply


Thread Tools Search this Thread
Search this Thread:

Advanced Search

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

vB code is On
Smilies are On
[IMG] code is On
HTML code is Off
Forum Jump

Similar Threads
Thread Thread Starter Forum Replies Last Post
New Discovery on Increasing Platelets - Papaya Leaves fibogann Alternative Treatments 23 Tue Dec 23, 2014 07:06 AM
HLA Platelets. Have Some Questions????? Grifmat Transfusions and Iron Overload 10 Wed May 1, 2013 10:37 PM
Low platelets S001 MDS 27 Thu Aug 23, 2012 01:07 PM
?WHY?- low platelets STILL > 1 yr post BMT MGirl Transplants 2 Sun Mar 25, 2012 01:46 AM
LOW platelets with reaction & Vidaza cheri MDS 6 Thu Nov 18, 2010 08:49 AM


All times are GMT -4. The time now is 05:34 AM.


Powered by vBulletin® Version 3.6.7
Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.
Forum sites may contain non-authoritative and unverified information.
Medical decisions should be made in consultation with qualified medical professionals.
Site contents exclusive of member posts Copyright © 2006-2020 Marrowforums.org