cost of copaxone in canada

Survey on the Impact of MS Disease-Modifying Therapies In late February, the Multiple Sclerosis Society of Canada will provide input on behalf of people with MS in regards to a review of the current and emerging disease-modifying therapies (DMT's) for MS taking place by the national agency that makes recommendations to provincial and territorial drug program decision makers.

I will be switching to Medicare when I run out of COBRA on my disability. I didn't know that about the price of Copaxone on Medicare. And it sounds like Teva/Shared Solutions doesn't work with them on it for the cost?

My Copaxone is about $1325 per month. I think my Neurontin is about $200/month for 720x300mg pills. Elavil - no clue and I'm too lazy to go look, but I will later. Both covered 100% by my provincial and employer insurance plans. How do those prices compare to elsewhere in Canada (I'm in northern Alberta), in the US, UK, NZ, Aus, etc?

Another company has a generic of Copaxone and is fighting in the U.S. courts with Teva. Ironically Teva fights in court to make generics of all the other best selling drugs in the U.S. Teva's marketing is expensive as is the whole Share Solutions organization which is to get and keep as many MS patients on Copaxone and to find out about problems with the drug before the FDA does.

Interesting discussion re: the pricing of MS drugs. I am quite surprised to see Copaxone priced at $5500 - $6000 per month at Walmart/Walgreen's in the US. Mine is priced at about $1600, though I don't pay anything out of pocket for it. http://www.healthline.

It is cheaper in Canada because the Government negotiates with the drug companies which the U.S. does not even do with Medicare the government run health program. In the U.S. drug companies spend millions of dollars on individual lawmaker's campaigns and on lobbyists. The Drug companies and Health Insurance Companies practically own the U.S. government. Teva make more money on Copaxone in the U.S. then any other place in the World.

1) Does it cost money in canada to meet with a counsellor? (don't really want to go to the meetings) Kind of looking for a step by step program type thing to keep me clean? 2)Can you keep it anonymous and not release your name?

That is insane, in Canada I had a csection, was in the hospital for 4 days and the only thing I paid for was my 14 dollar constipation meds.

Dear all, Good news to share with you: I have a terrific job offer... in Australia! (My current contract is temporary and, after expiring, I would be without insurance and possibly need to leave the country and head back home to my home country where treatment for MS is even harder and more expensive to find). The so-so news: As I've mentioned before, I was diagnosed with a CIS (optic neuritis) last April, and now I'm under Copaxone.

00 every month just for Copaxone. The other drugs cost another $400.00. This leaves me with a lot of year left when money runs out. Assistance Fund helped a year ago ,however they only help if you have know insurance. I think I was a mistake. Need help.

t afford Level III because I cover the family) with BCBS. With Level I, I paid the full cost, until I met the deductible, then the plan paid 80% of the cost up to the maximum out-of-pocket of $1200 (then the plan paid 100%). Now I pay a copay of $62.50 every three months for my Copaxone. You may also consider contacting Shared Solutions, MS groups (like MS Society, etc.) to help with this problem. There's a thread I posted on, which I will try to find, in regards to this.

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.

Hi. Are you in the US? If so, the answer to your question is that Teva, like all of the CRAB manufacturers, charges as much as it does because it can. It's that simple. They will tell you how expensive it is to research new drugs, most of which never pan out, and they're right. They do need to recoup these costs, and they do need to make a profit or they'd be out of business, and then we'd all suffer.

Yay! I for one AM switching treatments. Good-bye needles. Ordinarily I'd be in the 'stand back and see how it goes for others' group. This is different, for me, because the same drug has been used for years now in Europe to treat psoriasis. so there's a lot of track record out there. I know there can be side effects, not serious ones, and probably fleeting if they happen at all, and I'll have to deal with that if and when. For now, I'm just glad.

Similar results were reported from a different study examining the effect of COPAXONE® in Clinically Isolated Syndrome (CIS) patients. The study demonstrated patients who received COPAXONE® improved in their cerebral neuroaxonal integrity relative to patients treated with placebo. Patients on placebo showed a decline in NAA consistent with that demonstrated in historical control studies. 1. Khan, O. (2008).

This is what I did before my Dx i found out and explored what drugs i may have to be getting on a long term or forever basis, and what drugs alot of people on the forms are using ect. then, I checked all of them in my medical insurance book to see what tiers and co pays if they even cover some of them. (just in case I may need to use them in the future). I went to drug co.

I made an appointment with him for a second opinion and then treated in one of the Boceprevir trials. There are other new drugs in the pipeline currently in trials that you could speak with him about at your appointment. In the meantime do a search at www.clinicaltrials.gov using "Hepatitis C and Michigan". See what comes up then you can start your homework prior to your appointment. Best of luck!

You have copay assistance where you live through Copaxone? Capaxone the generic by another company will be on the market in the US one of these days and it might bring prices down. It might be available in other countries.

Cost of copaxone in canada

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