copaxone side effects hives

I've been on Copaxone for 3-4 months now. I don't really have anything to add that db hasn't already said about the site reactions and effectiveness of it. I will say that from my own experience with it, I'm happy with it. My sister was on Rebif, and had flu side-effects. That's why I'm taking Copaxone. Other than the site reactions, and a very very mild post-injection reaction (face became hot and flushed), I've not had any problems with it.

I'm wondering if anyone else here has had any issues with Copaxone concerning side effects other then the injection site reactions? I've been on Copaxone for 3 months now, I am agitated, frustrated, quick to anger. I've also been experiencing paranoia and mild visual hallucinations. I'm getting sick at least every 2 weeks, and have a general feeling of "un-well" or "ill".

I started using copaxone 20 mg a year ago and i had hot flashes sometimes,few days ago about an adverse effect after an injection of copaxone 40mg,I started with copaxone about 3 weeks and did not have any side effects but 4 days ago after my injection my entire body had a hot flash,subconsciously I started screaming and had problem breathing,it felt like the veins on the back of my neck were boiling,I kept scratching my neck and face because of hives!

Hey, Meg - what sort of problems are you having with Copaxone? I had the site reactions, which were red, raised welts (about three inches in diameter) that itched for three days. I also had the IPIR, which is an immediate post-injection reaction. After the fifth one, it began to resemble an allergic reaction (itching and swelling) so I discontinued it. But as far as I know, Copaxone doesn't cause any other reactions.

I've stopped taking methimazole 12 days ago because of the strong side effects (hives, joint/muscle pain, dry throat). Though these effects are lessening, I wonder how long it might take for them to be completely gone.

Before Avonex I was on Copaxone. I have to disagree with Lulu about no side effects. The first month or so was fine, but after that I began getting hives, bumps, lumps, rashes and horrible itching. The bottom line is that I developed a severe allergy and had to go off it. Virtually everyone here who's on Copaxone is contending with bumps and itching to some extent, but far far less than I had. So everyone is different.

those are definitely not listed among the side effects of copaxone - perhaps you really had some type of virus in your system making you feel bad? hope you feel better....

The rest of my hives seem to be clearing up. I use Copaxone by injection once a day and I have stopped it fot a few days also. I do need to start it again however. I have no idea what the connection might be. I would appreciate any feedback anyone might want to contribute.

This is a weird question, but I see you live in NY. I live in ct. Can i ask what the doctors found to diagnose you? I have been having a he'll of a time getting a diagnosis and I used to live in hampton bays. I saw river head and got excited. Sorry for the off question but I was just curious tht there may behold for me yet. Would you be qble to send me the name of your neuro?

oh yes these are some of the wounderful side effects of tx,do check with your dr.about your hives to make sure its not a reaction but my dr. put me on tiamcinolone cream for the rash,it does tin to help.

I'm on copaxone. I have to do a really small dose on my legs because with a full dose, I get lumps the size of softballs! I try to hang in there. Sometimes I give up and skip a week or 2 just to give my poor legs a rest. What was your reaction to copaxone? Having lupus, I can't do any of the interferons. My rheumie said with lupus my body makes interferon. My neuro suggested methotrexate, but that won't do because of my kidneys. Then he suggested tysabri.

I'm signed up to start Tysabri in the next couple weeks. My doctor really recommended it as he thinks it would be a good option for me. It's just kind of difficult for me to wrap my mind around because it seems like it's used more as a last resort rather than a first line of defense. This will be my first DMD, and I'm a little nervous. Is anyone else using this as a first DMD? What kind of side effects can I expect?

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.

s the most mild in reference to side effects and also for women of child bearing age (like me). Since day 1 of Copaxone, after EVERY single injection every day I get a horrible huge painful lump that swells up, is hot to the touch, hard to the touch, and becomes very very itchy. It almost looks like I am having an allergic reaction or cellulitis. I have tried multiple depth settings (making the dreaded muscle hitting mistake too low and the million times worse itching when it's too shallow.

d rather inject daily then deal with the Rebif side effects and increase in depression! I have been on Copaxone for a week already and the ONLY side effect I have had is injection site stinging. No fever, No sweats, No fatigue, No muscle pain, and No other flu like symptoms. I hope things get better for you soon! Take Care!

GG, the first medication I was on was Copaxone. After a few months, it caused SEVERE headaches that didn't respond to any pain meds. I realized that when I didn't use it I didn't have the headache or hives. If you haven't talked to your doctor about it, you might want to. My neurologist switched me to a different DMD (Tysabri) and am no longer experiencing any of the nasty side effects.

It can take a few months to separate disease activity from treatment side-effects unless its something obvious like Copaxone welts. Be sure to mention this to your team when you go for the second infusion so this gets put in your notes and you get feedback from the pros. In the mean time, I'm so sorry you're feeling this wiped out.

in addition to a few flu side effects, my lip has started twitching and was wondering if this too could be a side effect?

You should be fine starting the Copaxone while still on IVSM. For most people, Copaxone actually has very few side effects. If you feel comfortable sharing more detail about your concern we can be more specific with help. Welcome to our MS community. We’re always happy to see new faces even though it’s sad we all end up gathering here to deal with MS. I hope you hang around and we get a chance to know you better and help you through the rough times as you start living with MS.

The Copaxone rep called me yesterday to discuss my refills. I have some questions that maybe some of you can answer. She asked me if I was was still taking Copaxone or a different MS drug with Copaxone, or instead of Copaxone. In the 8 months I've been on Copaxone, I've never been asked this question before. I know the new pill is out, but is anyone here taking the new medicine? and if so... does it work, do you like it? why did you choose to take this?

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. I am losing my mind my flare up is so bad right now. Its like I want to crawl out of my skin.

All medicines may cause side effects, but many people have no, or minor, side effects. When used in small doses, no COMMON side effects have been reported with Tylenol. Seek medical attention right away if any of these SEVERE side effects occur when using Tylenol: "Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); dark urine or pale stools; unusual fatigue; yellowing of the skin or eyes.

Hello, Your symptoms are suggestive of hives. Hives (medically known as urticaria) are red, itchy, raised areas of skin that appear in varying shapes and sizes. They have a tendency to change size rapidly and to move around, disappearing in one place and reappearing in other places, often in a matter of hours. Many cases of hives are "idiopathic," meaning no cause is known. Others may be triggered by viral infections or medications. Treatment is by oral antihistamines.

Copaxone side effects hives

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