avonex cost per month

I just called my local pharmacy to get the price of my Avonex prefilled injector pens. For a one month supply which is 4 pens it cost $20, 456.00! That's $245472.00 a year! Thank God for insurance. With insurance I pay an $80 co-pay. We need a cure!

I just got the letter from Novartis about my share-of-cost for the oral drug Gilenya. I was astonished to see that they expect me to pay $150 per month. This amount is probably a result of what they negotiated with the insurance company, but I have good insurance and can't believe this is the best they can come up with. My neuro has a good reason for putting me on this drug versus going on the interferons and I'd hate to think I can't go on this because of cost.

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.

I guess since your big worry is the cost the first thing to give you is the phone number for The MS Active Support 1-800-456-2255. According to this it will only cost you $10 a month for your shots (not bad $2.50 a week). This phone number is 24/7 and can also get you to a nurse to discuss problems or side effects after you start. I like 24/7 because my problems don't happen between 9 & 5, lol!

Oh I think mine was per month though not per three months. The doc would write the script for 3 months worth but they'd only give me one month at a time, so 40 a month.

In NZ the cost is roughly between $1000 and $1250 NZ per month. It's fully subsidised so patients pay about $5 per month once they get approval for the subsidy. Are you guys in the US being ripped off, if it's so much cheaper in NZ?

I contacted my insurance company today to ask about the price of the meds for triple treatment. A 3 month supply of interferon, ribavirin, & Victrelis would cost $180.00 (so about $60 a month) I thought it was going to be a lot higher. But I forgot to ask about "rescue drugs". Not sure how that works and how much that would be. Any one have an idea?

Hi, I'm on Avonex, which is once a week. I just reached the full dosage, and the side effects are getting somewhat better: I still am very tired and ache some the day after my injection. I'm told that they will continue to lessen for another 3 months or so; if so, they'll be no problem. The company that makes it has a great program with people to talk to and help with financial assistance, a nurse to ask questions of, and so much more.

s oral, Tecfidera aka BG-12, is slated for US FDA approval later this month. This new dosing for Avonex may be an effort to cut down on MS Market cannibalism as people shift from Biogen's Avonex to BG-12.

I DONT GIVE MYSELF THE INJECTIONS EACH WEEK, MY HUSBAND DOES BUT THEY ASSISTANCE PROGRAM AVONEX HAS IS GREAT. WE PAID 10 A MONTH AND WHEN HE CHANGED JOBS AND WE LOST INSURANCE I HAVE BEEN GETTING IT FOR FREE. I DO STILL GET ACHY, EMOTIONAL BUT FEEL LIKE I AM ADJUSTING TO THE MEDICATION. GOOD LUCK WITH YOUR CHOICE. HOPE THINGS GO WELL WITH YOUR INSURANCE.

With only 10 to 30 grams of Sovaldi needed for successful treatment, the difference from the $30 production cost for Gilead’s full course of treatment—30 grams x $1.00 per gram—to $84,000 for the 12-week treatment program represents a retail markup of 279,000%.) Weinstein’s letter to state Medicaid directors also reminds them that, “Gilead did not pay to research and develop Sovaldi. In 2011, it purchased Pharmasset, the company that had already developed the drug, for $11 billion in cash.

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.

Our cost right now will be$1750 per month then medicare will only cover the 750.

No one covers it, but many insurance companies have lowered the cost. It cost me $225 a month last year and this year is down to $85 a month. There are also clauses about medicare bumping you off their lists and so on, so read the fine print and save some time later.

So, I paid $1715 last month and again this month. Then I get to drop down to $172 per month for the rest of the year. Yes, in this time of recession, the Robber Barons continue to get richer. Oil, Insurance, Pharmaceuticals, Bankers. In general, it's not a good time to be sick or poor. Where's my silver spoon?

i pay 300 per month in copays for treatment. Each injectable is 100 per month and I'm on 3. 700 is pretty steep but that's the way things are going in healthcare. A year ago my co pay on neupogen was 45 a month.

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?

Shared Solutions has various financial assistance programs available, including copy assistance for anyone who is insured but has a copy over $35 per month (I use that one myself). If she has no insurance at all, a call to the National MS Society may help her find some assistance from private sources.

Has anyone every gone off the Avonex--& if so how did it go? Wanting so badly to quit the shots! Been doing them since '98 & it's getting hard to get the needle through the skin on my legs. I went from '78 to '98 with no episodes & was diagnosed then. That was with no meds of any kind for that 20 years!!

i know one lady i talk to said they ended up paying 300 per month. with the special authority do they pay the whole cost?

My insurance company will NEVER go for 4K a month! They fought about Avonex at $3K a month! Will the government ever get a grip on these Pharma companies and realize if we can't pay for it-we won't be around to pay their payroll. This is shocking news, no matter what I decide-again..my life is in their hands again. Very depressing.

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?

00 with 2500 deductible. Luckily my avonex only cost me 10.00 a month due to the fact the I qualify for patient assistance based on my income.

Avonex cost per month

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