betaseron generic

I am sure your company tells people it is the same as the Betaseron, but just like a lot of generic drugs, they may use different formularies or compounds, [[ Example, my Mom can not take some generic drugs ,and one in particular would make her throw up-- That being Vicodin HP, she has been taking a long time for her Hip replacements.

My insurance prescription coverage only covers generic drugs and since there is no generic drug for Copaxone it would cost me $10,000 for a 3 month supply! I obviously do not have that kind of money, not really sure who could afford that but anyway... I was working with Shared Solutions and their medication assistance only to be told that I was inelidgeable for the assistance.

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.

m not on betaseron, but am glad to hear you are making a change to see if you can find a combination to slow your MS. Getting the new MRI done on the stronger machine is so important for your baseline... it will give your new neuro a good view as to where you are coming from. And you're right, it might show where you have new damage that is causing your changes.

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.

When I visited with the MS specialist, I mentioned my odd angioedema - whenever I got an injury to the face (usually either the dog bumping me in the lip, or biting my tongue) and the phlebitis in my leg. I also talked about the blood clot I had just recovered from. She went ahead and got a test for lupus anticoagulant, which was positive. Now, those people who test positive for the lupus anticoagulant don't necessarily have lupus.

My Neuro wants me to switch from Rebif to Betaseron. I have been taking Rebif since March 09 and have had to do one round of Solu Medrol in May and will find out tomorrow if I have to do another. I also have pretty bad injection site reactions which is why the Neuro wants the switch. I guess Rebif has acid in the injection and it makes the site reactions worse? My question is, I am under the impression that Betaseron is not pre mixed and also that there is not an auto injector?

ve wondered about Copaxone since my blood clot, which happened when I switched from Copaxone to Betaseron - the first week. And my angioedema symptoms, which were beginning to resemble antiphospholipase syndrome (until I stopped taking Copaxone.

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.

He did warn me about the miscarage risk. The last visit, he said to get off Betaseron 1 month before ttc. The BetaPlus nurse said give it two months. My husband and I discussed this. The current plan is to get off the Betaseron at the end of next week. That would be 2 wks in to the last pack of bc pills. We are planning to use alternate methods of bc for the next cycle. That would put me off of Betaseron 8 wks prior to the hoped for conception, and off the bc pills for 6 wks.

I saw on your other post the mention that they want you to take Rebif instead. Be sure that your neuro is fine with that - they are both interferons and work the same way.

Pretty much said I wouldnt be sitting there looking like this if I had been on meds (not sure that that is entirley true only a 30% chance in my opinion) She gave me the option of another med covered by my health insurance which is Betaseron. Gave me the CD to watch and sent RX to pharmacy. Of course I come home and read all teh possible side effects and its making me want to do nothing now. I am so med paranoid (and Im a Nurse for Pete's sake!

Hard to answer your question without more information. Why do you have only those four choices? 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.

I have been on Betaseron since 1995. I have not had an attack since I started using the Betaseron. 3 1/2 year ago I slipped on the stairs and landed hard on my tailbone. A pain shot up through my back and gave me a terrible headache. Over the next few days, my leg started going numb. Went to the doctor and he sent me for x-rays and gave me muscle relaxants. Nothing on the x-ray. Sent me to my neurologist. He examined me and said it was MS and had me take three courses of solumedrol.

So the doc tells me I don't have a UTI. That's the good news. The bad news is that I'm still experiencing muscle spasms and spasticity on Betaseron. I thought this would go away when the fever resolved, but it hasn't. Who else on here is taking Betaseron (or some sort of interferon?) And if so, did you have problems with muscle stiffness, and did it resolve?

I too read in an article or publication on APS and MS. I've read that MS patients can have a low to medium positive result in the anticardiolipin IgG or IgM who are on beta-interferons.. It also stated a significant fraction of patients with true MS may have positive serology for IgG or IgM anticardiolipin antibody. My research has stated via Neurology books (googled them and you can get snippets of pages) that there are people with MS who have positive serology for IgG or M.

I am going to be starting Betaseron soon. I have read up on it quite a bit, but am curious to know if any of you are currently taking this, have been on it, etc... and if so, what was it like for you? My biggest concern about this one is that everything I read warns of extreme depression. That is already a daily struggle for me, pretty bad. Sure hope I don't get worse with this medication. I hate getting in those ruts of depression. For me, it can last for months on end...

I started on Betaseron within a month of the diagnosis. I have symptoms from the old lesions but never had another clinical exacerbation. I stopped taking the Betaseron after 6 years (two months ago). Two more MRIs after diagnosis showed no new lesions. The second MRI (a year after diagnosis) looked like "classic M.S." (I was told by an M.S. specialist). The third MRI (last year) showed some of the lesions were smaller. Question: by whatever criteria is being used now, is this M.S.?

My Dr. wants me to start the new oral meds after the baby is born. I was on Betaseron for one year before we conceived. In that year, I had three relapses that required steroids. He said that ment that the Betaseron was not effective. One of the relapses really does not caount against the treatment because it was the 10th week of the treatment. I guess I am ok with trying the new meds. What do you all think? Would you try it? Do you think that it is a good idea?

s had problems with holding her urine. At times it will just come out. She was put on a med. from the Vet. Does anyone know of a generic brand or natural one that will do the same. I can't keep going back paying office visits everytime she needs a new med.

I have never had any luck when I have been placed on the generic brands of medications. Celexa especially; I was on it for 10 years, tried the generic several times and paid for it. 3. I have also been on Neurontin for the past 10 years. In a past post, I wondered if they decrease in dosage is what was causing me so many problems. However, I am back on the brand name of the medication and there's a HUGE difference between the two.

He said that he believes in a higher dose - high frequency shot....either rebif or betaseron. His preference is betaseron....ultimately more meds being injected than Rebif, and much lower instances of injection site problems. The negative is slightly higher chance of antibodies being built up. The efficacy is about the same. So the MS specialist said Betaseron and we now have a box of the stuff sitting on our kitchen table. How did you end up with Rebif?

Both medicines you list have strong safety profiles and stood the test of time (although the Extavia brand is newer, but I believe is is the same as Betaseron), as have a few other medicines you don’t list. And you can always change your mind later, although you should give a drug at least a few months to work. And yes, there’s a chance it might not work out for you, but MS progression definitely won’t work out for you, and so you are right to try to attack your MS with something.

Betaseron generic

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