Avonex copay assistance

Common Questions and Answers about Avonex copay assistance

avonex

am working on the $. If I didn't get any $ assistance, it would cost me $35 copay for a month's worth (4 injections). That's not bad, as I was expecting it to cost a lot more. This is do-able but $ assistance would be great especially since my husband lost his job. I like to hear personal stories about avonex (w/o the sugar-coating part) & have been getting some. I would rather know all the bad stuff ahead of time. Fear of the unknown bothers me a lot. Thanks again. Be well.
All of the CRAB (copaxone/rebif/<span style = 'background-color: #dae8f4'>avonex</span>, betaseron) drug companies have patient assistance programs, if they are needed. I recommend calling your insurance first though, to see what their preferences are- because with mine, they wanted me to try certain ones first, before they would agree to pay for the others. I have know idea why, and neither did the agent I was speaking to. There aren't any generics available for these drugs. With a prescription from your doctor, you should be okay.
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. for me the side effects from the Betaseron have been much more tolerable than the side effects from avonex. I still have my miserable days but they are not nearly as rough as with avonex.
I have been on copaxne for several years but need assistance with the co-pay- Are there funds and if so hhow do I access them?
com/patients/about_betaseron/affording_betaseron.jsp but here's the fine print ..... * Some restrictions apply. Copay assistance is limited to $9500 per patient per calendar year. Patients who are enrolled in any type of government insurance are not eligible. Patients are required to report any benefits they receive, e.g. copay refunds, to their insurance company. Void where prohibited by law, taxed, or restricted. Patients enrolled in Bayer's Patient Assistance Program are not eligible.
One is a financial assistance program that helps you with the cost of your copay - for example, my copay was $90, and they helped me out with $40 of it. When I had problems affording the $50, I talked to my neurologist, who helped me with a complete financial assistance program that would allow me to get it for free. However, Aetna is a complicated mess. I have to get all my medication through their Specialty Pharmacy, not their mail-order pharmacy, which is confusing.
They do have some programs that will help with your copay. I do get my rebif from Walgreens and only have a copay of 9.00. I decided on Walgreens instead of getting it by mail. I was worried about the side effects and did not want three months of rebif at one time just incase my body would reject it. I will eventually get it through the mail because my copay will be 9.00 for three months.
I cant afford the drug - the maximum shared solutions will give for copay assistance is $500 per month (which is alot of money but it still leaves me with a monthly cost of over $1300 - and that's just for copaxone!
market, will be more expensive than injectable competitors such as Biogen Idec Inc.’s <span style = 'background-color: #dae8f4'>avonex</span>, Merck KGaA’s Rebif and Teva Pharmaceutical Industries Ltd.’s Copaxone, which cost between about $2,800 and $3,200, for a standard month’s supply, according to the Web site destinationrx.com. “Gilenya pricing is based on the value it will deliver patients, the scientific innovation it represents and our investment in studies to support the product,” Althoff said. The U.S.
ladies, if you are paying a copay for the cellcept, be sure to see their website for financial assistance. They have a card you use at the pharmacy good for $100 a month on your copay. http://www.cellceptforliving.com/ I tried to read more about cellcept but have run out of time for now. Hopefully someone with experience will come along and help. about those warnings - absolutely everything these days come with lengthy, scarey warnings.
I called the number this morning and found out exactly what you said Ann, there is no copay - Its Free! I was hopeful they would bringthe copay down ideally to below $50, but then the nurse told me that I was approved for the copay assistnace and that it would be FREE. They said this free copay arrangement is good till December 2011. I am relieved. Oh and the $125 or 150 I was seeing in the letter was for any medical expenses I had encurred getting the medical screenings, i.e.
Note - I don't know about avonex, but REBIF has free treatment for the first year for everyone who picks it (in the US) - <span style = 'background-color: #dae8f4'>avonex</span> has patient assistance, but I don't know the details. TEVA pharmaceuticals also has a progam to assist with the co-pay costs from certain pharmacies.
The pharma companies could all take a clue from Bayer Health and work this out. A copay assistance program for EVERYONE would be wonderful. OR maybe all of us should make the switch to rebif? Believe me when I say this is something I am considering.
Rebif had one to lower your copay or give you the drug free for a year. I know that Copaxone has a form of financial assistance that you can apply for. I'm applying now to see if it'll help (no income or medical insurance here, yay). If that doesn't help, I'd talk to the doctor or his/her office to see if they know of any programs or call the MS Society. There are tons of programs out there. National MS Society website http://www.nationalmssociety.org/index.
I am just starting in the next few weeks with <span style = 'background-color: #dae8f4'>avonex</span>, $1800.00 per month, but with my works extended health,Bio Gen assistance and then Pharmacare i will have to pay a miminal amout..under $100.
The injectible MS meds, as well as the new oral meds, are very, very expensive, but most do have good financial assistance, if you qualify (and each pharma company has different rules for assistance). So, there's lots of homework to do. Good luck. Ask if you have more questions.
I got sick of fighting with the pharmacy and Copay assistance. Bad reason I know, but since I have PPMS I am not that worried. Alex.
did you try for copay assistance program for <span style = 'background-color: #dae8f4'>avonex</span>? they paid my prescription deductible. I pay just 10.
I'm a Medicaid queen. There is a 5.00 copay at doctors/specialists office visits and sometimes, depending on what brand of medication Im getting I have to pay at least 5.00 to 8.00 (like provigil).
I finished my last dose of iv Solumedrol. I start 2 weeks of prednisone tomorrow. He gave me a support kit for <span style = 'background-color: #dae8f4'>avonex</span> which will be a once a week injection. They said its expensive but they have financial assistance that can help with cost. A nurse will come over and show me how to give myself the injections. (scary!) Does anyone else have experience with this medication?
In the United States it doesn't give you the most bang for your buck - my copay for <span style = 'background-color: #dae8f4'>avonex</span> for 3 months was something like $60. My Tysabri cost, after Medicare and United Health Care AND getting Tysabri assistance for the drug (I could get it for $10) ended up being over $600 PER INFUSION. I asked and asked and asked what the charge would be before I started - and they said after insurance probably $50-60. They would NOT give me a number.
Another thought, which may be a dumb one, is to try to get into some clinical trial, one of the safer ones, such as taking Copaxone and <span style = 'background-color: #dae8f4'>avonex</span> together (as one of the possibilities). I'm hoping other forum members have some more original ideas. People????
Biogen, the maker of tecfidera is very good with financial assistance. I am currently on <span style = 'background-color: #dae8f4'>avonex</span> and they have been very supportive, both with financial help, and with any medical questions about the medication or side effects. I am both nervous and excited to start because I have had side effects from the avonex since I started last July.
Novartis is offering an assistance program. If what you are on works, by all means stay on it, but if not, I would definately push to try it.
Since you are clinically definite, I'd recommend getting on a therapy soon. The interferons (<span style = 'background-color: #dae8f4'>avonex</span>, Rebif, and Betaseron) all work pretty much the same way. Copaxone is a copolymer, that acts as a myelin decoy. Did your neurologist give you any choices other than these four?
Aside from my late shipments, I once stopped Gilenya after a 19-day trial and waited four or five more weeks to restart <span style = 'background-color: #dae8f4'>avonex</span>. I had intense side effects for a week or two, much like when I first started avonex long ago, but otherwise there was no problem.
Thank you for your time and help.
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