rebif cost per month

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.

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?

s more than 5000 soles per month (more than 2000 $) ... If anyone knows a similar case or have any information about it I 'd appreciate it. Thanks.

Hi, There is no great source of information available in Singapore although I can tell you that Rebif will cost you around $7,000 for a 3 month supply or you can now get the new oral medication Gilenya which is taken orally everyday and costs around $130 per pill. No cheap treatments available here! My husband currently sees a Dr. Alvin Seah at Raffles Hospital perhaps if you call them they can give you an idea?

my MediCal was changed whne my daughter turned 18, leaving me with a 585 co-pay per month, which i don't have since i can't work. I am on rebif. I contacted ms lifeline and they sent me an application for assistance with rebif costs. because of my income (or lack thereof) i was granted a year's worth of rebif.

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.

I don't know if you will be approved or not but there is a two year wait for Medicare after you begin receiving it. Sometimes they do back date it. I waited only a year. If you are dx with MS, trust me...go to their website and get their number. Ask the operator there for someone in financial assistance. They have a program that offers the best assistance for those in financial need. There are two kinds of assistance programs...

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.

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?

All the rebif paraphanalia is supplied free as well, however the drug costs $1945.00 per month where I live. Thankfully I have medical insurance. Yes, the ease of injecting makes it less of a chore. Sllowe - The device I'm using is not the rebiject, it's the RebiSmart, a fully automated electronic device that does everything. I'm still tritating (the rebiSmart does that automatically) I took my 6th shot Sunday @ 8.

Wish, I was told copax is now $3,5000 per month/30 syringes. Fortunately I do have good insurance and only pay $50 for my copay each month ($600/year). It doesn't sound too bad but I am on other $50/month drugs as well and boy does it add up. All the drug companies have programs to assist in one form or another with the cost if you don't have insurance.

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?

through an employer or similar group plan, may have their plans combined to reduce or eliminate any co-pay. Those on income assistance ('welfare') will have DMDs provided at no or nominal cost (such as tina295 was provided before her benefits were discontinued). Anyone having trouble accessing MS drugs for financial reasons, which is unusual in Canada, should contact the MS society.

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.

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?

There is help available for the cost of DMDs - some from manufacturers and some from the NMSS I believe. Cost should not be a hindrance to getting something that can help you!

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.

Hi there, I am currently on Rebif (9 months into it) but would love to try Tecfidera. My annual neuro exam is in a month and I think I will be making the switch at that time. A little concerned about the gastro issues that some experience because I do have GERD but if my health insurance will let me switch then I will hopefully start Tec in June.

I have just started a 5 day infusion course and I have a really dumb question. Should I continue with Rebif during treatment ? Dx 1988 but it's been at least 10 yrs since last steroid infusion...

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.

I work 45 hours/week at my full-time job and about 5 hours a week at my side job and NEED the job/insurance to help cover the more than $4,000/month that my medications cost.

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

0T might show new lesions but we will not know if they are new or its a better image and just see more. My doc might not even pick up on that and say Rebif is not working when it might be!! I got the 1.5T, so I won the battle. However now i wonder if I was right?? What do you think?? BTW Oct MRI looked pretty good and Dr thinks Rebif is working!! This is just a follow up double check. Sorry I may have said that before.

I have been on rebif 44 for 9 weeks. Two weeks ago I started biting my lip. I noticed that my jaw is jerking which makes me bite my lip. Also started biting tongue. It is like my tongue does not know where it is. Does anyone else have this problem. I am taking the rebif for ms.

After a further conversation with the clinic nurse, I settled on Rebif and started on it approx 3 months after my dx. I was actually ready to start it within a month of my dx, but the MS clinic was putting off calling in my prescription because they wanted me to have full drug coverage in place before starting (through the provincial MS Drug Program in Alberta).

Rebif cost per month

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