Home Menu

Site Navigation




advertisement
NeuroTalk Support Groups > > >

Tysabri Information and Check In part 2

Closed Thread
Page 13 of 75 « First 31112 13 14152363 Last »
 
Thread Tools Display Modes
Old 07-13-2009, 10:30 PM #121
Natalie8's Avatar
Natalie8 Natalie8 is offline
Member
  
Join Date: Apr 2008
Posts: 900
15 yr Member
Natalie8 Natalie8 is offline
Member
Natalie8's Avatar
 
Join Date: Apr 2008
Posts: 900
15 yr Member
Default
Does anyone know what the wholesale cost of one dose of Tysabri is right now? Thanks!
__________________
On Tysabri and love it.
.
Natalie8 is offline  

advertisement
Old 07-14-2009, 01:54 PM #122
Harry Z Harry Z is offline
Member
  
Join Date: Sep 2006
Location: London, Canada
Posts: 241
15 yr Member
Harry Z Harry Z is offline
Member
 
Join Date: Sep 2006
Location: London, Canada
Posts: 241
15 yr Member
Default
Quote:
Originally Posted by Natalie8 View Post
Does anyone know what the wholesale cost of one dose of Tysabri is right now? Thanks!
The wholesale cost of Tysabri is just below $ 2400.00 When it was initially released, the cost was just over $ 1800.00. But Biogen had to pass on their extra costs from fixing their hasty release to someone!

The big expense comes from the infusions which range anywhere from about $ 2500.00 to over $ 8000.00!!

Harry
Harry Z is offline  
Old 07-14-2009, 05:36 PM #123
Natalie8's Avatar
Natalie8 Natalie8 is offline
Member
  
Join Date: Apr 2008
Posts: 900
15 yr Member
Natalie8 Natalie8 is offline
Member
Natalie8's Avatar
 
Join Date: Apr 2008
Posts: 900
15 yr Member
Default
Thanks for the price quote. Although my infusion costs $498 a pop. That's a far cry from thousands of dollars.
__________________
On Tysabri and love it.
.
Natalie8 is offline  
Old 07-15-2009, 09:00 AM #124
Harry Z Harry Z is offline
Member
  
Join Date: Sep 2006
Location: London, Canada
Posts: 241
15 yr Member
Harry Z Harry Z is offline
Member
 
Join Date: Sep 2006
Location: London, Canada
Posts: 241
15 yr Member
Default
Quote:
Originally Posted by Natalie8 View Post
Thanks for the price quote. Although my infusion costs $498 a pop. That's a far cry from thousands of dollars.
Is that what you pay for the infusion or what the insurance company is billed? I haven't heard of infusion costs this low. The highest cost I've seen is from one MS patient in Alaska who was paying about $ 8000.00 per session!!!

Harry
Harry Z is offline  
Old 07-15-2009, 10:15 AM #125
ewizabeth's Avatar
ewizabeth ewizabeth is offline
Elder
  
Join Date: Sep 2006
Location: northern Illinois
Posts: 5,258
15 yr Member
ewizabeth ewizabeth is offline
Elder
ewizabeth's Avatar
 
Join Date: Sep 2006
Location: northern Illinois
Posts: 5,258
15 yr Member
Default
I heard that Rush in Chicago charges more than 10k per infusion.
__________________
Wiz

Turn Left at the next election.
.


RRMS DX 01/28/03 Started Copaxone again on 12/09/09
ewizabeth is offline  
"Thanks for this!" says:
Natalie8 (07-15-2009)
Old 07-15-2009, 12:40 PM #126
Grammie 2 3 Grammie 2 3 is offline
Member
  
Join Date: Aug 2007
Location: Colorado
Posts: 374
15 yr Member
Grammie 2 3 Grammie 2 3 is offline
Member
 
Join Date: Aug 2007
Location: Colorado
Posts: 374
15 yr Member
Default
Quote:
Originally Posted by Harry Z View Post
Is that what you pay for the infusion or what the insurance company is billed? I haven't heard of infusion costs this low. The highest cost I've seen is from one MS patient in Alaska who was paying about $ 8000.00 per session!!!

Harry
I get my infusion either in AZ or CO at hospitals-they are paid approx $490 per infusion and $2,000 for med-this is thru Medicare.
Grammie 2 3 is offline  
"Thanks for this!" says:
Natalie8 (07-15-2009)
Old 07-15-2009, 01:44 PM #127
Natalie8's Avatar
Natalie8 Natalie8 is offline
Member
  
Join Date: Apr 2008
Posts: 900
15 yr Member
Natalie8 Natalie8 is offline
Member
Natalie8's Avatar
 
Join Date: Apr 2008
Posts: 900
15 yr Member
Default
I wasn't clear enough. $498 is billed to my insurance each month for the infusion process. This does not include cost of drug which I get through my prescription drug plan through a specialty pharmacy. I have Blue Cross Blue Shield PPO.

Maybe it is less expensive since I get it at my doctor's office and not through a freestanding infusion clinic? (they do call it an infusion clinic though since other people are around me getting it too).
__________________
On Tysabri and love it.
.
Natalie8 is offline  
Old 07-15-2009, 02:39 PM #128
Harry Z Harry Z is offline
Member
  
Join Date: Sep 2006
Location: London, Canada
Posts: 241
15 yr Member
Harry Z Harry Z is offline
Member
 
Join Date: Sep 2006
Location: London, Canada
Posts: 241
15 yr Member
Default
Quote:
Originally Posted by Natalie8 View Post
I wasn't clear enough. $498 is billed to my insurance each month for the infusion process. This does not include cost of drug which I get through my prescription drug plan through a specialty pharmacy. I have Blue Cross Blue Shield PPO.

Maybe it is less expensive since I get it at my doctor's office and not through a freestanding infusion clinic? (they do call it an infusion clinic though since other people are around me getting it too).
I'm still trying to figure out why one infusion center will charge about $ 500 for the process and we read some charge as much as $ 10,000.!! Doesn't make any sense at all.

Harry
Harry Z is offline  
Old 07-15-2009, 04:14 PM #129
lady_express_44's Avatar
lady_express_44 lady_express_44 is offline
Grand Magnate
  
Join Date: Aug 2006
Location: Vancouver, Canada
Posts: 3,300
15 yr Member
lady_express_44 lady_express_44 is offline
Grand Magnate
lady_express_44's Avatar
 
Join Date: Aug 2006
Location: Vancouver, Canada
Posts: 3,300
15 yr Member
Default
Quote:
Originally Posted by Harry Z View Post
I'm still trying to figure out why one infusion center will charge about $ 500 for the process and we read some charge as much as $ 10,000.!! Doesn't make any sense at all.

Harry
Some infusion centers are run by the very same neuro's that recommend that their patient "needs" Tysabri. Wonder if that makes a difference ...?

Cherie
__________________
I am not a Neurologist, Physician, Nurse, or Hairdresser ... but I have learned that it is not such a great idea to give oneself a haircut after three margaritas
.
lady_express_44 is offline  
Old 07-15-2009, 05:08 PM #130
Chemar's Avatar
Chemar Chemar is offline
Administrator
Community Support Team
  
Join Date: Aug 2006
Posts: 28,459
15 yr Member
Chemar Chemar is offline
Administrator
Community Support Team
Chemar's Avatar
 
Join Date: Aug 2006
Posts: 28,459
15 yr Member
Arrow
just a reminder that this dedicated thread is intended for those members who use Tysabri as a treatment, or who are considering using it, but not for other members who may have comments against its use, who do not themselves use it

If you are not someone who is on this treatment and you wish to start separate threads below on your views/comments of this drug, feel free to do so(provided they conform to the guidelines of NT) but please do not post them on this sticky thread unless you are a Tysabri patient.

thanks
__________________
~Chemar~


*
.


*
.


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.
Last edited by Chemar; 07-16-2009 at 06:31 PM. Reason: clarifying
Chemar is offline  
"Thanks for this!" says:
ewizabeth (07-15-2009), Natalie8 (07-15-2009), Riverwild (01-11-2011), SallyC (07-15-2009)
Closed Thread
Page 13 of 75 « First 31112 13 14152363 Last »

« Previous Thread | Next Thread »

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
LDN Information & Check-in 2 SallyC Multiple Sclerosis 827 07-07-2017 09:46 PM
Tysabri Information & Check In Curious Multiple Sclerosis 988 04-16-2009 05:09 PM
LDN Information & Check In SallyC Multiple Sclerosis 844 01-15-2009 11:40 AM
Part 2...Medicare Part D/Prescription Coverage Stitcher Parkinson's Disease 1 12-17-2006 12:50 AM


All times are GMT -5. The time now is 03:36 PM.

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.

 

All posts copyright their original authors.

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.

Home