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Betaseron and alcohol

Common Questions and Answers about Betaseron and alcohol

betaseron

Avatar f tn Identify liver disease, especially cirrhosis and hepatitis caused by alcohol, drugs, or viruses. Help check for liver damage. Find out whether jaundice was caused by a blood disorder or liver disease. Keep track of the effects of cholesterol-lowering medicines and other medicines that can damage the liver.
Avatar f tn t know the rates for Avonex and Betaseron but I believe they are similar) . I was in this bottom 3% and after two attempts, ruling out any other possible culprits (normal baseline, then no alcohol, supplements or any other medication for the trial run on Rebif), I went off Rebif at the advice of my neuro, who treated this all very seriously, and went on Copaxone June of 2008. My liver enzymes promptly returned to normal, and I am tolerating this med well ; it has no neg effect on the liver.
233622 tn?1279334905 I have been off of Betaseron for about 2 weeks now and my eyes are back to being very uncomfortable. Before I started Avonex eye pressure and pain was a huge problem. Now it is is starting again.
338416 tn?1420045702 re taking your Coumadin for the positive serology for a positive serology of aCL IgG/IgM and Reynauds and taking Betaseron for your MS (even prophylactically while waiting for a diagnosis) that it can cause a little anxiety. It's one medication counteracting another. I would be concerned too. Are you going to talk to your doctor about this?
Avatar f tn at first it was just like spotting but now its aot like a period (as of today). I am on betaseron and I didn't know if it could mess with your period like tha or make your breasts sore.. (fatigue is a normal ms symptom tho so that doesn't concern me except its been worse lately). Plus.. I have been noticing that its harder for me 2 hold it when I have to pee and smetimes it leaks (which again could be ms related). I'm just worried and really can't do a test yet..
Avatar f tn Hi and welcome. What a good question. I have no idea what is a teratogenic agent and can't investigate that this morning because I have to get ready for work. But I don't want you waiting for more replies until later today. What I do know is I have heard this discussion before- most of the time in reference to the woman being on treatment. The topic of the man on MS disease modifying drugs has also been discussed but the answers are much less clear.
Avatar f tn I've been on Betaseron since a year after I was diagnosed in 2000. On August 20th, I quit taking Betaseron cold turkey when I finally received my new oral medication Tecfidera. For the last few days I have been dealing with horrible body aches, diarrhea, cold sweats & the inability to eat (not feeling sick, just not being hungry or interested in eating). I do not have a fever, a cough, allergies or anything else I can conclude to be at fault for these annoying symptoms.
Avatar f tn I'm three weeks into Betaseron . . . and am pleased to hear all of the positive news.
Avatar m tn d be getting your dr to sort out this problem for you. To me its part of his/her job to get you what you need and if Betaseron is what you need, he/she should hopefully know how to get it (back) for you. Cheers.........
Avatar f tn The specialist at UCSF is switching me to Tysabri and has told me to go ahead and stop my Betaseron. It has now been 2 shots that I missed (well didn't take) and for the past 2 days I have been feeling like someone beat the crud outta me. My husband is insisting it is cuz I am not taking my shots. I don't see how that can be. We went to UCSF Monday night (4 hr drive), had my Dr appt Tues which took 4 hrs.
338416 tn?1420045702 Well, as some of you guys may remember, I had a blood clot in my leg last October. This was right behind my right knee, which is the knee with all the problems - weakness, numbness. I also have phlebitis in my left leg. I also have Reynaud's, apparently since 2009. Well, I hadn't been taking my Betaseron, because I'd read some anecdotal evidence that indicated there was a connection between blood clots, reynaud's, and Betaseron.
1967803 tn?1325679473 ve been trying to figure out what to do about health insurance. My neurologist and I were discussing Betaseron and gawking at the out-of-pocket cost. Luckily he was nice enough to waive the fee for my next visit, but we haven't figured out a solution for the medication. He told me to come back when I got insurance so I could get a proper diagnosis and a prescription. Does Medicaid cover Betaseron?
Avatar f tn I have been on Betaseron for 2 years with no side effects and am happy with it. Obviously with the NHS I have no choice about the change. Any insight would be greatly appreciated.
1770663 tn?1313992050 Hi tammy and welcome to this side of the diagnostic mountain. I'm sorry you have joined our dx'd club, but at least you have a name for what is bothering you. As for the prescription, Alex and Julie are so right that you can let the neuro's office take the next go at your insurance company. Please do not despair about this glitch - if nothing else, there are patient assistance programs from all of the pharmaceutical companies that will also help with the drug cost.
1950519 tn?1324518193 Kate, Tysabri is not the last option there is Gilenya and and few Chemo therapy drugs. There are also a few new drugs in clinical trials. If you look up MS drugs there are a few besides the CRABs and Tysabri.
1002640 tn?1280746685 I am extremly frustrated and not sure what to do. I guess Im looking for others out there who are using Betaseron and what your thoughts/opinions/reactions are? Im tired of being tired and tired of the unpredictibility of this flippin disease. Oh and she tells me your "probably looking at a 3 month recovery time from this relapse" great, how the hell am I supposed to take care of myself working full time...
Avatar f tn I used Betaseron and now Gilanya. I have better results so far with gilenya. Origionally, I chose Betaseron over Avonex because I would rather have less side effects more often that be completely wiped out once a week as a mother of little ones. The Gilenya does not seem to cause such a problem. I hope that you can get the med that best suits you approved with your insurance. Sometimes the doctors office has to get ugly with the insurance on your behalf. Best wishes to you!
Avatar f tn Avonex (which I’ve used for 11 years) and others are notably absent from your list. Avonex, Rebif, and Betaseron have been around longest and have the strongest safety profiles. If your MS is more aggressive, then you may be more inclined to consider Gilenya, Tecfidera, Aubagio, or Tysabri. All of the DMDs are discussed from a neutral perspective at the link below: http://www.nationalmssociety.org/Treating-MS/Medications Choose a medicine that you can adhere to the dosing schedule.
Avatar f tn I did take a test to make sure I have not developed antibodies to the Betaseron and I have not. I had an MRI of my brain and it showed only old lesions indicating that I have not had an MS attack in many years. What else could be the problem?
338416 tn?1420045702 I started having muscle spasms on Friday. My right leg was spasming so much that I couldn't walk! And the spasm across my chest was making it difficult to breathe. On Saturday I started taking two Baclofen at a time, just so my leg would shut up just a little bit. It was still a little painful to breathe, although nothing like Friday. I couldn't complete a full step with the right leg.
Avatar m tn I have MS and Neuropathy. I am currently on Tysabri. Previously I was on Betaseron and IVIG. When I went to Tysabri my doctor took me off IVIG and now my Neuropathy is worse, my feet and legs are on fire. Does any one know if it is safe to be on Tysabri and IVIG at the same time? My doctor said she would need to consult with other doctors before she would add IVIG to my treatment.