Glatiramer copaxone

Common Questions and Answers about Glatiramer copaxone

copaxone

Avatar n tn COPAXONE®(glatiramer acetate injection) copaxone (glatiramer acetate) injection [Aventis Pharmaceuticals Inc.] DESCRIPTION ... Patients should be instructed on the safe disposal of full containers ... dailymed.nlm.nih.gov/dailymed/archives/fdaDrugInfo.cfm?
382218 tn?1341181487 New data presented provided evidence that long-term treatment with COPAXONE® (glatiramer acetate injection) may offer sustained protection from neuronal/axonal injury. This protective effect was reflected biologically by a significant increase in N-acetylaspartate (NAA), a specific marker of neuronal mitochondrial function, in treated versus non-treated relapsing-remitting multiple sclerosis (RRMS) patients.
7463086 tn?1391008763 Just read that the FDA has approved Copaxone to be given at a higher dose 3 times a week as apposed to a lower does every day. This med is one that I was considering starting for treatment. Does anyone have any thoughts or informationabout the dosage or even the medication?
1831849 tn?1383228392 Teva is testing Copaxone at twice the current level. The results ore given relative to placebo. Nothing is said about results relative to current dose. http://www.nasdaq.
1713150 tn?1314467342 Hello everyone! I Haven't really been on here much lately. Just going through some new changes in my life. I'm doing well, how are you guys? You all are always in my prayers and I hope all is well as can be! :) I started taking Rebif almost 2 months ago and haven't had any problems with it, except a new kind of fatigue coming around latley like the day after I take it because I take it at night right before bed. And I know this has more to do with the MS than the DMD, I think.
Avatar f tn Some folks on theis forum have had it happen. I have been on Copaxone for about 120 days with no issues related to the Copaxone.
Avatar f tn I was looking at copaxone but read studies that it increases the risk of breast cancer being an immuno suppressant so I am very scared. It also says it can cause weight gain and people have painful injections with huge hives and welts. I looked at tecidferca too and know girl s who couldnt push through the side effects if stomach pain and flushing they were so bad. I am very scared. Please help with any advice especially if you are on the drug. Not sure they are worth the risk.
572651 tn?1530999357 Full story Glatiramer-IFN Combo in MS a Toss-Up NEW ORLEANS -- Radiologic findings from a closely watched trial of glatiramer acetate (Copaxone) and interferon-beta-1a (Avonex) combination therapy in multiple sclerosis were mixed, a researcher said here.
198419 tn?1360242356 Keeping up on topic wants (studies)...Oral versus injection is down right exciting! http://www.mscare.org/cmsc/News/CMSC-INForMS-Biogen-Idec-Announces-Positive-Top-Line-Results-from-2nd-PIII-Trial-of-Oral-BG-12. "BG-12 met the CONFIRM study's primary endpoint by significantly reducing annualized relapse rate (ARR) by 44 percent for BID (p< 0.0001) and by 51 percent for TID (p< 0.0001) versus placebo at two years.
Avatar f tn I had the same thinking as you when I started Copaxone. I decided my abdomen had as much right to a left and right division as my limbs do. That gives eight general areas that I simply rotate around. It's worked well for me. I don't try to match the day of the week to a specific body part.
Avatar f tn My neuro describes the difference between the interferons (betaseron, rebif and avonex) and glatiramer acetate( copaxone) as similar to a pepsi/coke challenge. they are all the same, it just depends on personal preference as to which one you like better. Is your doctor offering you copaxoneThe side effects we know from copaxone, after 18 years of use, is the lipotrophy. Period. There are no liver problems. No difficulty with drug induced depression. You do have to inject daily.
382218 tn?1341181487 The ongoing US Glatiramer Acetate (GA) Trial is the longest evaluation of continuous immunomodulatory therapy in relapsing–remitting multiple sclerosis (RRMS). The objective of this study was to evaluate up to 15 years of GA as a sole disease-modifying therapy. Two hundred and thirty-two patients received at least one GA dose since study initiation in 1991 (mITT cohort), and 100 (43%, Ongoing cohort) continued as of February 2008.
378497 tn?1232143585 Treatment with glatiramer acetate or the interferon may limit the number of new black holes that became permanent; i.e., reduce progression of brain atrophy, and the interferon seemed to be slightly better at it. There is no control (i.e., untreated) group for comparison of how well the ************** worked vs. no treatment at all.
Avatar n tn Also a study published in the August issue of Neurology showed that Copaxone® (glatiramer acetate for injection) reduced by 50 percent the percentage of permanent "black holes" that developed in patients with relapsing-remitting multiple sclerosis. Black holes are lesions MS can cause in the brain, and these lesions, if permanent, represent areas where the most severe and irreversible brain tissue damage has occurred.
Avatar m tn The most important thing to put the flare into a silent mode, and recover! My sister will start her MS treatment. In first line she have chosen copaxone (glatiramer-acetate), she dont want to experience flu like sympthoms so she rejected betaferon, and avonex. In second line (if the first line treatment ineffective) she may chose tysabri (natalizumab) or gilenya (fingolimod). Fortunately RRMS'ers nowadays have a lot of effective treatments to fight against this desease.
1637739 tn?1371688706 It showed 2 new active lesions which concern my neuro and he suggests changing my DMD. I have taken Copaxone for the past year of which I still have some reactions to. Any suggestions as to which DMD I should try next? The neuro would put me on Gilenya if I wanted. I am concerned that since Copaxone didn't work, that the other injections might not as well. Not to mention, I am scared to try the them!
Avatar n tn With that said I have no issues in the past 10 years and the Optic Neuritis cleared up years ago. I was on Copaxone but stopped taking it 5 years ago. I have been issue free, med free and stable MRI's over the past 5 years. I have not told my doctor I stopped taking the medicine (shame on me) but every time I see him he says everything is in check and I am doing great. Was thinking of going to a different doctor just to start over and be up front.
Avatar n tn Over 20 years ago, at the age of 22, I was diagnosed with primary progressive MS. My method of coping was DENIAL! Since the doc was wrong, (I actually have relasping-remitting), and since the course of my disease was so mild (although I've had repeated exacerbations and relapses, I've always had nearly complete recovery in a matter of weeks), living in denial has worked well for me for a long-long time. In Jan '08, I lost the sense of taste across about 2/3 of my tongue.
1983221 tn?1333506185 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.