Two words - Patent Protection :-) Just Kidding!
Avonex is protected through 2026. I think the main reason for the addition of Plegridy is the dosing. You anly need to inject every other week.
I wonder why they didn't just market a 'new and improved' Avonex, like Teva did with Copaxone. It seems as if that would have been cheaper for them in the long run.
I follow most developments regarding MS fairly well, yet Plegridy fell off my radar at warp speed. I'm betting that's true for most others, if they've even heard of it to begin with.
I was just reading on MSAA about another topic but noticed an August 2014 update on Plegridy and thought you might be interested......
The every two week dosing is why my neuro suggested it and I tolerate Avonex okay. I really wanted to do an oral DMD but after discussion we decided Tysabri was the way to go. While I have not had a relapse He is concerned about disability. Waiting for my first infusion will let you know hoe it goes.
Hi JM -
Many, myself included, tolerate Tysabri very well. The once a month dosing was a bonus for me. Keep us posted.'
It seems like we have similar issues with the meds. I was dx in 2011 and was on copaxone for 2 yrs and then I developed an " allergic reaction" to it which manifested itself as swollen and somewhat painful inguinal lymph node. Did you have the same problem? After that I was on Avonex for 8 months and tolerated the medication fairly well, but had hard time injecting long needle into the muscle (I used the injectors for both copaxone and avonex). I'm now on Tecfidera almost 6 months and still have GI issues so in addition to Tecfidera I'm taking Omeprazole (Prilosec) for my stomach. I'm also wondering about Plegridy and how does the new injector works.
Well actually our problems with Copaxone were quite different. I started benignly enough, just severe stinging at the site for a while, but things got worse quickly. Skin reactions became horrific--welts, bumps, hives, rashes and bruises. And incredible, incredible itching. At any one time I'd have five or six places that were driving me nuts from itching, and I tried every topical agent and allergy med out there.
I know nearly everyone gets some skin issues at the injection sites, but this was off the charts, and my neuro said I'm allergic, it will only get worse, and to stop the med. Whew. I do have quite sensitive, fair skin, and I think any 'shallow' injection would be a problem, maybe not as bad as Copaxone, but still....
So then I was on Avonex for years with no skin reactions. Mostly pre-medication with an NSAID prevented the flu-like stuff, but not always. This never got better, as it does with most people. Not too bad on the whole, I have to say, but shots are far from fun at the best of times.
I was off the DMDs for a while, longer than I'd planned, for various reasons, including coming down with flares just when I wanted to try something else. I really wanted to be on an oral med if at all possible.
My neuro didn't want to prescribe Gilenya for me, as I'm pretty old and there apparently can be cardiac effects in my age group. That was fine with me, considering side effects people complain of, here and elsewhere. So Tec was the choice.
I did the first week low dose/thereafter high dose thing as is standard. After I'd been at 240 a few days, I began to get 'distress in the lower tract,' as they say on TV, or used to. Nowadays they come right out with 'diarrhea.' This was pretty bad, to say the least. I was going to be away from home off and on for several weeks at that point, so my neuro and I decided to hold off the Tec till I would be here pretty much all the time.
Finally, after problems not with insurance but with an insanely incompetent specialty pharmacy (CVS/Caremark--that story would be a long post in itself), I started back on Tec, but this time my neuro ordered the 120 dose for 4 weeks instead of 1. That I did, and am now happily at 240. No bathroom issues, no flushing (hah!) no nothing. Or at least thus far, knock on wood.
I've been on Omeprazole for GERD for years. That apparently, for me, has nothing to do with success or failure with Tec. My neuro told me to take Imodium if needed, this time around, but it hasn't been needed. He also said that people who have only occasional digestive issues with Tec likely are skipping doses or otherwise not being compliant. I have no way of knowing whether that holds up. But of course, there were some during the Tec trials, who discontinued it because of these effects. A small percentage but still some. You could be one of that group.
Are you having your blood checked regularly for white cell count? Also, liver enzymes should be monitored, but as to the white cells, it's important that they stay at a good level to fight infection. If this isn't familiar to you, please see my post of a week or so ago, about Tec and a death from PML.
I was on Avonex for 17 years and was sick in bed one day a week for that entire time. When Tecfidera came out I was thrilled to try the pills but my neuro took me off them after three weeks because they made me violently sick with vomiting and diarrhea to the point of being hospitalized twice for dehydration. I have since been on Plegridy for the last 3 1/2 months and it has been nothing like the Avonex. I get an annoying injection site reaction that lasts up to a month but I do not get sick. I don't know if its because its subcutaneous or not.