Betaseron cost

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betaseron

* Novartis gained the rights to seek approval for its own branded version of interferon beta-1b through agreements with Bayer Schering, the company that markets Betaseron. Betaseron is marketed under the name of Betaferon® outside the US. Betaseron and Betaferon are registered trademarks of Bayer Schering Pharma AG.
//pagingdrgupta.blogs.cnn.com/2010/03/29/scientists-find-there-may-be-two-forms-of-multiple-sclerosis/?
Hi, I would like to know, if anybody knows a good and caring neurologist in Stanislaus county? Also is there any program for receiving free or very low cost Betaseron.
Hi All I saw my neuro on Thursday, told him it would probably be my last visit, as i now have no insurance, he wants to keep me on the 50MG of Prednisone for the rest of the month then taper me down gradually to perhaps 5mg a day within 8 months My Concern is that he wants me to start Betaseron again, and i really do not want to go there, I still have shot sites that are healing from 3 months ago, that's when i stopped taking the shots, as ii was having a bad reaction to them he has decided t
Posted By jack lewis on July 29, 1997 at 10:43:29: In Reply to: Betaseron vs. Avonex posted by Katheryn on July 16, 1997 at 19:36:03: : July 16, 1997 Question: What is the difference between Betaseron and Avonex? Thank you. As far as I know, as a MSer with chronic progressive MS, I take neither of these drugs since I do not have the exerbatting-remitting form of the disease.
I'm stressing about the cost of drugs. I don't even have a ballpark idea of what this is going to be like. I guess none of these drugs go on the first or second tier of my prescription coverage formulary. What happens if you don't have the money? Do some DMDs cost less than others?
What plans cover at least some of the Rebif cost? My copay with Humana was about $300 per month. Would like not to exceed this amount.
How did you find out that your insurance company doesn't want to cover the Betaseron. Did the Betaseron people tell you that?
My classmate and friend, who is also the pharmacy tech where I pick up most of my prescriptions, blurted out an expletive when she saw how a one-month supply of Betaseron injections cost ($4600). Luckily my co-pay was $1 through Medicaid, which I'm eligible for so long as I remain a dirt poor student. As much as I want to be cynical about big pharmaceutical companies, I had a $10 co-pay through Bayer's Betaseron patient assistance program when I was without insurance.
The deal with MS drugs is the better they work at slowing progression the more dangerous they are because at the same time they suppress the immune system. Yes and the cost of all are very high. I had to weigh the cost against the cost of caring for me if I just allowed the illness to progress. If your illness is progressing rapidly Tysabri is an option. The others are equal in safety and effectiveness.
Okay so my neurologist says to look at Gilenya and wants to start this in the next week or so. I decide to compare cost. I am amazed at the cost of the cost of the Betaseron. Been out since 1993 and the cost is still over $30,000 per year, REALLY!!!!!! No wonder there are those who choose to not take the DMD and treat the relapses. If my copay is 20% can you imagine???????
I am on Betaseron every other day. I talked to the insurance company this week and it only covers 50% of the 2000.00 the injections costs each month. I do have a cap of 2500.00 and then insurance picks up 100%. I do NOT have the 2500.00 up front it is going to take to get that 100% insurance coverage. So this is all being looked into and the drug company will let me know if I qualify for their copay assistance program. I better or I will have to go off of the medication.
GTL I would like to hear from MS patients regarding their experiences in dealing with the various manufacturing company call centers - Betaplus (Betaseron), Shared Solutions (Copaxone), Patient Services (AvonexAvonex Avonex prefilled syringe & Tysabri), Others?. What do you like and don't like? What services are important to you vs. which are not? What are your pet peeves and how do you suggest we fix them? Thank you all!
My insurance prescription coverage only covers generic drugs and since there is no generic drug for Copaxone it would cost me $10,000 for a 3 month supply! I obviously do not have that kind of money, not really sure who could afford that but anyway... I was working with Shared Solutions and their medication assistance only to be told that I was inelidgeable for the assistance.
I just received my letter stating that I can receive Betaseron for $50 a month. We have to pay up front on our insurance, so I filled out the form for patient assistance (upon Betaseron rep's recommendation). I found the form by googling "Betaseron Patient Assistance Program". Have you been directed to the form?
December 09, 2011 The manufacturer of a major drug for multiple sclerosis has given what appears to be a money-back guarantee that its product will prevent severe relapses when used as directed.
( I also don't know if it's such a good idea to go the uninsured route and get Betaseron covered by the pharm company. I like that I could get it low cost/free, but I feel like this is a really bad time to be uninsured plus I'm clinging to my neurologist like a deer in headlights and he doesn't come cheap.
My gait is somewhat labored, I have intention tremor in my hands and some numbness on my left side. I am considering stopping my Avonex becausse of the cost. Have not seen my neurologist yet but want another persons opinion also.
Through the MS LifeLines Access Made Simple program, you may be eligible to get Rebif® (interferon beta-1a) at no cost, or for no more than $50 per month, for up to one year of treatment. Best of all, MS LifeLines takes care of all the paperwork.... http://www. mslifelines. com/rebif/insurance/ access-made-simple. jsp?intcmp The following assistance programs info provided by MSAA...msassociation.
And if you've read through trial results from the main CRABs (copax, rebif, avonex, betaseron) your probably burnt out from data and stats. To put your mind at ease, in the long-term they are equally effective and all DMDs aim to reduce relapses and progression by one mechanism or another. Short term they have shown to reduce relapses by 30% (on average). Many Drs ask that you consider dosing schedules, which is very important.
The national agency - Canadian Agency for Drugs and Technologies in Health (CADTH) is currently undertaking a systematic review to compare the efficacy and safety of DMT's for patients with relapsing-remitting MS and will examine their cost-effectiveness.
Hey Guys and Dolls Research about to be puplished, gives clear indication that treating first attack (probable MSers) with DMD's is the better patient out come, than waiting for a second attack and therefore the patients becomes CDMS and dx, before providing DMD treatment. [Clear-Cut Dose Response There was also a "very clear-cut" dose response, noted Dr. Freedman.
The cost of this drug should not keep you from getting this treatment - the way our medical care is paid for in this country is another rant for a different day. My mother uses Enbrel for arthritis and it has made a world of difference, but it is expensive and she pays about $350 out of pocket each month too - and she is 85 years old!
Generally only tier 1 is totally free of co-pay and that would cost me an additional $$ premium. To take advantage of that FREE generic, I would have to figure up how much I usually spend for generics and see if it is lesser to upgrade. Your basic question. NO, DMD drugs are not generic, they have not been around that long and my personal opinion is that I do not want generics "messing" with something that crucial to my health.
It is not recommended to use these medications in any way except for their approved dosage. If the cost of the medication is the issue,contact the drug companies. Most of the drug companies have wonderful cost assistance programs now. Even Tysabri is offering a $30 a month plan.......Good luck but I hope you talk her out of it.
What is usually the cost of these meds? ( I am considering trying Rebif or Avonex) I have heard they run about $1500/month. I have to meet a $3000 deductible which means I may have to pay for my first dose. I don't have an extra $1500 floating around. I am really starting to freak out! But then again part of me figures I have probably had MS for 15-20 years an I am fine so far. I guess waiting another 1-2 months to start taking DMDs can't hurt. Can it?
I have tried for years, and particularly for the last year siince having been on Medicaid, have cost the taxpayers thousandds of dollars having tests and appointments which have not brought me on step closer to answeres or even feeling better. The pain and muscles weakness is getting so bad that I just dont feel that I can function even on a minimal level anymore. Yesterday in church I had to sit during singing and lean my arms on the chair in front of me just so I could clap my hands.
Avonex (IM qwk ), Betaseron (sq qod), Copaxone (sq daily), Rebif (sq 3 x wk) and Betaferon (sq qod) The committee is presenting to the Medicaid board on June 24th, with a recommendation to limit access to Copaxone only. The MS communtiy may not be aware of this at this time and they need help to stop this limitation of meds. All of these meds have flu like side effects, shot site reactions, and all require injection.
Last time they basically told me it wouldn't be covered, followed by the 1,,000s it was going to cost to stay on it the very next month. Then a follow-up letter stated it would be. So, I simmered for the better part of this year over it all, and NOW they sent a new one. Rebif is not on their "preferred" list. And, they told me to give a form they sent which says "Avonex, Betaseron, or Copax" are preferred, and my doctor is to fill out the form.
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