copaxone launch

Has anyone heard if and when Teleprevir will Launch in the US? I am from Canada...............Was UND at the end of my treatment and Post TX...... have relapsed..........now have to wait for the new Meds in Canada to be approved.........I have a specialist that I will call............interesting..and cannot seem to get any straight answers about anything Thanks all!

The BEYOND trial compared the effectiveness of three treatment arms (regular-dose Betaseron, double-dose Betaseron, and Copaxone®) in 2244 patients with RRMS. The primary endpoint was relapse risk, and all three treatments showed a robust, equal effectiveness (average follow-up time was just over two years). The annualized relapse rate fell by almost 80 percent, compared to the year prior to entry.

The supply of the Hepatitis C drug to Vertex by Shasun Chemicals is set to take off earlier than anticipated. The product is set to launch in June-July next year. "Commercial supplies have already started and we are preparing for the launch this year," says Vimal Kumar, Managing Director of Shasun Chemicals, in an exclusive interview with CNBC-TV18's Udayan Mukherjee and Mitali Mukherjee. . Who Is Shasun Pharma ?

http://www.mmm-online.com/incivek-to-set-record-for-fastest-blockbuster-launch-analyst-predicts/article/215925/ "Vertex's drug for treating hepatitis C virus, Incivek (telaprevir), is on course to smash the previous record for the biggest revenue-generating drug launch ever." "The direct-acting antiviral generated $494.1 million in sales from its US launch in May through the end of September, Vertex disclosed recently in an earnings report.

5 months ago i started to had a digestive system problems symptoms like bloat and feeling of fullness they said to me i have a colon problem then i had gerd after that and feeling of heartburn i took ppi like omeprazole and when i stop it the gerd symptoms appear again and with all of these symptoms i feel numbness sometimes in my left head and my arms and legs come and goes and my breath is shorten without reason and globus sensation in my throat !

Hey, My son has tactile defensiveness--we are patiently awaiting the launch of this company: Soft! www.softclothing.net It's designed by a mom and a special educator--produced by a dad of a child with Autism. They are doing everything seamless, tagless, organic, etc... the stuff looks adorable!!! I hope this will make my mornings easier. This discussion is related to <a href='/posts/show/277948'>Tactile Sensory Disorder</a>.

t go away after being off the Copaxone we decided the two were unrelated and I started taking Copaxone again, last night was my first injection after the break. My question is - last night I woke up feeling like I had the flu, I was sweating, ached all over and had a massive headache. I know these are side effects of the interferons but has anyone had this while on Copaxone? I had no reaction like this the first few weeks I took Copaxone.

//www.ehealthme.com/ds/copaxone/hallucinations,+mixed "On Aug, 31, 2013: 9,277 people reported to have side effects when taking Copaxone. Among them, 5 people (0.05%) have Hallucinations, Mixed." the most recent was one person in 2011. It would be difficult to prove hallucinations were a side effect of copaxone, based on those very small numbers. There are no withdrawal symptoms from going off copaxopne.

because this study, like many others, was supported by the drug co. that developed, produces, markets and distributes Copaxone. So I guess we take the info with a grain of salt, and hope that the study was designed appropriately and objectively, and that results are reported accurately and ethically. If so, and the encouraging results are repeated in future studies, then it really would be great news for Copaxone users.

I have never heard of this side effect from copaxone and not sure how it could effect your cycle. Anyway, I had a hysterectomy way back when so I couldn't have this symptom regardless. Sorry.

Did they tell you that you had optic neuritis? That was my first flair as far as we know. I've had it 3 or 4 times. I don't remember. I went on prednisone a few times and it worked every times. Lately, for the past few months off and on, I've been having jumpy vision. It gives me pretty bad migraines. I get migraines very easily so I'm on daily meds for that as well. It seems to work well but it doesn't stop the things that trigger my migraines.

Hello, I am sorry that I am saying this, I was pre-diagnosed with ms that was recently confirmed not ms. I am sorry that I had the news that most of you reading this will not hear. However I had accepted the diagnosis and was prepared,to move forward with my newly found life. And as a result almost a year of injection copaxone treatment ms that I don't know what to do with. I hate to throw it away but am not sure if I have another choice. Does anyone know of any other options?

Started my Copaxone on May 24 and it was fine and had no pain to speak of injecting.

Hi Ali. I can tell you my experience with Copaxone. I was just diagnosed in Dec of 07. I haven't been on any other MS med. I was put on Copaxone. In those 3 months I struggled with depression, sleeplessness, gained 10 lbs and had terrible dark circles under my eyes. It completely changed my personality. I took myself off it and finally after 2 weeks am starting to feel like myself again and have dropped the weight and the circles under my eyes are gone.

Copaxone is made by Teva Pharmaceutical Industries Ltd. For more information, visit the Copaxone website, or call Shared Solutions at 1-800-887-8100.

But, I have just recently wondered about a question about weight gain. I am paranoid about gaining weight, and for some reason have not really thought about this issue when discussing the DMD's. I was actually relieved that someone finally is doing something about my situation. Anyways, what my question is ...... Has anyone experienced weigh gain, and if so, how much is expected?

Anyone out here using Copaxone? And if so for how long. I think I am going to try it, and was interested in some first hand information. shots, side effects, if you think it is working, etc. Any information would be greatly appreciated.

I am SO glad that you posted this...I have noticed (just started Copaxone about 5-6 weeks ago) that I do have changes in my tastes. In fact, not long after I give myself an injection, I notice a strange taste in my mouth, almost like thiere is increased saliva production. This is probably TOTALLY my imagination... Yes, there are injection site reactions. I was getting BIG welts when I injectied with the auto-injector. I decided to try an experiment and go back to self-injecting.

I was reading the question that were posted about copaxone and I am currently on my husband insurance and my copay is $40.00 a month but they pay $5.00 and I only pay $35.00 a month. Well my situation is changing and I really need to find a way to pay for this medicine. I check with my insurance on my job and it will not cover this medicine. I need help. I read this other lady post and she said they told her she didnt qualify, that is what I am afraid of.

Hi guys, this is a question for us users of Copaxone. I am wondering if anyone knows the reason we have to pinch up our skin before doing a manual injection? I am asking because some of my sites are easy to do that, but some are not. I have just been injecting , like anyother needle, and my reactions are minimal. Am I doing something wrong? With the Autoject, the reaction sites were just to sore, and lumpy, and I'm trying it this way..... \\\\\\\\So, what do ya think??? Thxs...

Copaxone launch

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