Skip to Content

User Reviews for Copaxone

The following information is NOT intended to endorse drugs or recommend therapy. While these reviews might be helpful, they are not a substitute for the expertise, skill, knowledge and judgement of healthcare practitioners in patient care. Learn more about Copaxone.

Filter by:

User Ratings

10
   
34%(37)
9
   
28%(30)
8
   
10%(10)
7
   
9%(9)
6
   
4%(4)
5
   
4%(4)
4
   
2%(2)
3
   
6%(6)
2
   
2%(2)
1
   
5%(5)

Copaxone Rating Summary

7.9/10 Average Rating

109 Ratings with 107 User Reviews

What next?Compare all 92 medications used in the treatment of Multiple Sclerosis.

Reviews for Copaxone to treat Multiple Sclerosis

Sort by:

"I was diagnosed wiht relapsing remitting multiple sclerosis (RRMS) in 2009. Started Copaxone 20 mg. Used auto inject..Had injection site lumps, itching, bee sting like reaction always. The skin began to atrophy. Had the immediate post-injection reaction (IPIR) too many times to count. Can't breathe, flushing, back spasms, terrible headache, chest pain... was switched to 40 mg because of lack of injection sites a few years later.. IPIR was THE WORST I've ever experienced. Stopped taking it for about 6 weeks. No exacerbations since my diagnosis. While off the meds I started having more nerve pain. My MS Dr said to switch back to 20 mg. I had a bad reaction last night w freezing shaking and joint/muscle pain for an hour. I have 4 injection sites left to use. Hips and flanks. Don't want liver trouble from other meds. Stuck."

Stuck.. (taken for 5 to 10 years) November 18, 2017

0 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"Taking 40mg 3x week for RIS, scans show MS but don't yet have a clinical diagnosis. Some welts and one large bruise but otherwise shots (all self inject) have been OK."

   
5.0

Basisforhope (taken for 6 months to 1 year) October 11, 2017

0 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"Diagnosed MS 2/2015; problems started 12/2014 1st Tecfidera: @4-5 months, many side-effects, horrible flushing, medicine worse than MS, t-cells plummeted. 2nd Copaxone: @ 2 months: hypothermia (one time very serious), and infections; @9 months, mammogram showed calcification. Pre-filled needle is thick and painful; syringes are poorly made and slip, causing pain; big lumps at injection site. 3rd Wahl's protocal (level 1 w/supplements) and Radical Remission protocal: All symptoms resolved, am better now than any time I can remember. I look forward to MRI next month, will be about 1 1/2 months off meds at that time, and 11 months on Wahls & Radical Remission lifestyle."

   
7.0

Anonymous (taken for 6 months to 1 year) August 28, 2017

5 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"Started taking Copaxone 16 months ago- no major side effects until last two months , On two occasions MS Nurse thinks I may of injected into bloodstream - uncontrollable shaking and chills - my husband almost called an ambulance. Neuro wants me to start Aubagio but I would like to trial the MS diet first on a 3 month trial.I don't know what to do !"

ciara77 (taken for 1 to 2 years) August 25, 2017

2 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"Doctor and I, together, decided to begin copaxone 40 mg after having been on copaxone 20 mg for 6 years, gilenya for 6 years (survived viral Encephalitis after this drug). Almost immediately, my joints began to stiffen and became painful ... so much so that lifting and using my hands is very difficult. It feels like I have arthritis in my joints. The nurse and the MS clinic informed me this is a 2.7% reported side effect. Now trying to detox my body."

   
6.0

Gilenyasurvivor August 20, 2017

4 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"Hey all! I was diagnosed with MS 25 years ago. I was on no meds for 15 yrs, Copaxone 20mg for 5 yrs then switched to Gilenya for 6 yrs. Then 2 weeks hospitalized with viral encephalitis!! Do not go on immune suppressing MS drugs!! I agree with others about the Wahl protocol... eat to feed your brain. Also include cardo, strength training and stretching weekly. I am starting Copaxone 40 mg. Should be no problem. "

   
9.0

FiftySue July 15, 2017

12 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"Took about 20 injections no effect yet"

Adge (taken for less than 1 month) June 25, 2017

2 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"I was diagnosed with MS at 41 in 1998..I was relieved when my doctor recommended the once a week shot Avonex thinking it would be the easiest. Not so...bad side effects. I went from cane to walker to wheel chair to hospital all in the few years I was on it. Just before I went into the hospital I went on 20 mg seven days a week of copaxone. It gave me my life back. I then went from wheel chair to walker to cane and then nothing in about two years time.. I've now been on it for 17 years with no major relapses. Not a day goes by that I don't feel the effects of MS but nothing compared to what it was before copaxone.."

   
9.0

Fdriver May 29, 2017

23 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"I was on the 20 mg of Copaxone for more than 10 years and took a break for about a year. Felt that I was stable, I felt great, and MRIs were showing no new progression. Recently starting trying to get back on it using the 40 mg for the last three weeks and am getting rashes, hives, headaches and in general feeling worn out and "MS-ey." Just not sure whether to be on it or not at this point."

   
8.0

Lindsey 333 (taken for 10 years or more) April 12, 2017

12 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"I was diagnosed relapsing-remitting Multiple Sclerosis MS April 2016. August 2016 and February 2017 the MRI showed minimal activity. My neurologist advised me to start using Copaxone, 3 times a week - 40 mg. I've been injecting myself without the auto injector and so far so good. I only inject in my belly and legs (in the evening). When injecting in my belly I experience a burning/itchy feeling. This fades away after an hour. It's an awkward feeling but not a big deal. When injecting my legs I experience stiffness of my leg muscle. After a few hours it is gone. The stiffness is a nuisance but not a big deal. Next morning, no more itchy sensations or muscle stiffness. All gone. Because I am only using it for 2 weeks I don't know if it helps but so far I am very happy"

   
8.0

Dreads March 17, 2017

10 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"I started taking copaxone in 2001, after trying avonex for 3 weeks with bad flu like symptoms. I began copaxone 20 mg once a day, it's been 16 yrs now with minimal side effects, compared to the exacerbations. I miss aprox 1 injection a week, on average due to it not injecting. I have not had a major attack in 16 yrs. I rarely ever use my cane. Once last year I caught the flu and had bad MS related symptoms. When I was 21 I had optic neuritis, @ 28 I became at least 90 percent paralyzed from my waist down and was told I would be in a wheel chair by 50. After this l quit smoking, drinking and any non medicinal drug, I began working out etc.The answer to me is the opposite to burning the candle at both ends & a positive outlook."

   
9.0

Lion heart March 1, 2017

22 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"I was diagnosed with RRMS in 1993. Tried Avonex, worst side effects body pain, pounding headache instantly. Stopped drug after 6 wks. In 1999 had relapse. Double vision, numb on left side, slurred speech, dizziness, fatigue, unable to walk without falling, my mind felt odd. Doctor at DUKE university suggested Copaxone 20mg. Started in 1999. Now on 40mg 3 times a week. Had relapse may 2016. I have itching, welts, injection pain, lumps and permanent indentations."

   
8.0

PJams (taken for 10 years or more) February 5, 2017

15 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"I started taking Copaxone in mid-August 2016. The first 3-4 months, I didn't notice any real difference. After the first few weeks, I didn't have any more site reactions. For the last two months, I'm experiencing terrible joint pain. Leg cramps in the middle of the night, my hips are stiff; my shoulders hurt. just a little while ago, my hand was shaking sooo bad. It's scared me. So here's the thing - I'm not experiencing any of the other MS symptoms that I had before taking Copaxone. Gone are those electrical shock sensations, I'm not really more numb, the weird feeling that runs down my spine. It seems like I've traded one set of symptoms for another. Before copaxone, I enjoyed exercising. Now not so much. :("

   
5.0

Linny60 January 24, 2017

17 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"I stopped copaxone due to bad reactions. I haven't eat red meat, milk, cheese, yogurt and white bread. I only drink almond milk and try to eat heathy. I am also taking vitamin d 5000 mg, cranberry pills 3600 mg, turmeric pills, fish oil, b12. I been heathy even without injections. Also praying a lot "

   
1.0

Menymom September 13, 2016

43 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"Have been on Copaxone 20mg everyday for 14 yrs. Only one major flare up in 2011 that left me numb from waist down, had to learn to walk again. But only missed 5 days not taking Copaxone. Am okay with a shot everyday. Am now walking with a walker, no flare ups since 2012."

   
10

Ms Owl 53 (taken for 10 years or more) September 10, 2016

21 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"After dealing with the horrific side effects of Avonex, and being admitted into a hospital for four days after I was suspected of having PML due to my worsening of symptoms and low white blood count (thanks to Tecfidera), I finally found the right treatment for me. I couldn't be any more happier with Copaxone."

   
10

AnttiKokko (taken for less than 1 month) August 19, 2016

32 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"i have been taking copaxen for 5 years now for ms i started the 1 a days shot but a year ago went to 3 a day this stuff kept me ms in check if you get this drug i suggest you get a auto injector with it makes things easer"

spinningblades July 7, 2016

34 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"Was on Copaxone for 3 years. Horrid reaction after many injections as it seemed I was often hitting a vein. Huge welts from injections that took weeks to subside. Last straw was the killing of flesh on left arm. Surgeon said damage looked like a chemical burn from the inside out. Two surgeries to repair and have 8 inch scar as permanent reminder. This was back in 2003."

   
3.0

Spool (taken for 2 to 5 years) June 23, 2016

21 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"I wrote a review on 12/2015 unfortunately I had to stop using copaxone because I got bad reactions. The last one was body shaking like if I had a machine connected to my body for one hour my buttocks muscle shaking so much. I got very scared and stopped medication. It's been 2 months and I don't think I will go back to it. I am just trying to eat healthy I cut all lacteos and red meat. "

   
3.0

Monicdmompho May 21, 2016

30 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"Please, anyone with MS, look into Dr. Terry Wahls and her protocol for MS. Most MS symptoms can be controlled through diet. Please take a few minutes to look into this, it could save you a lot of suffering and money."

   
7.0

NaturalHelper May 16, 2016

51 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"Have been on copaxone 20, avonex, and tysabri.Avonex caused bigiminy, tysabri was stopped because I had the virus and could have a brain infection. Copaxone has kept me free of relapses for 12yrs. I recently started copaxone 40 and have had 2 massive injection site reactions and am currently off treatment. I hope I can start back on copaxone 20, in 6wks. I am a lucky person, I am weak and tired, at 67 doing ok. I do not recommend copaxone 40,but do not want geneticists."

   
9.0

Glenn alex3 May 9, 2016

24 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"I had two pretty worrying initial exacerbations in July 2011 and February 2012; since then I use Copaxone and I've had no relapses nor new lesions (I write this May 2016). Injections are of course a nuisance, but what can we do."

   
8.0

Diego's May 8, 2016

32 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"I have been on Copaxone for 14 years. I have been fortunate in not having any more major flare ups and have remained fairly stable. I do have the tiredness and lack of energy at times, but sometimes feel so good I can almost forget I have MS. The first 12 years were the 20 mg daily injections and had the usual problems with site injection lumps and itching. I was changed to the 40 mg 3 times per week approximately two years ago and recently went to two injections per week because the insurance coverage is changing. I am going from my regular insurance to Medicare with a supplemental plan and will not have to pay $4,000 per year out of pocket. In my opinion I felt the best doing the 20 mg daily than taking 40 mg 3 times/week."

   
8.0

repool April 26, 2016

37 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"I experienced 2 attacks within 2 years. The Last was August 2014. On November 1st 2014, I was diagnosed with MS. I started Copaxone 40, 3x a week. Fast Forward to now, 4-25-16. I have had no new attacks since and no permanent damage. Sure the injections are a pain sometimes, and I was nervous at first. Plain and simple - If I mess up an injection. It Hurts! If I take my time and do it right I feel nothing. I have never dieted in my life, but now 38, I need to change my diet and exercise again. The medicine has worked for me. Aside from my weight gain, I am 100% grateful for the drug and will keep it going. Stay Positive ! Good Luck everyone. "It is what we make of it""

   
8.0

Anthony7707 (taken for 1 to 2 years) April 25, 2016

55 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

"I was diagnosed in 2004 and I've been off and on Copaxone since then. I take the 3x a week 40-count shot now, and there is a study ongoing now that is trying to see if taking an 80-count injection once a month works just as well. I always feel better on Copaxone, and I will try to remain compliant. In the past I've had muscle stiffness, anxiety w/ it, but not now. I find I have less site reaction if I inject it chilled, and stomach is best. Multiple studies have show it's the best chance to avoid a relapse. I do wonder, if I had remained compliant, whether I would be able to walk without a cane, or avoid the burning legs that make it hard to wear most pants. (I find medical cannabis hugely helpful, but I would prefer the no-high variety.)"

still walking (taken for 10 years or more) April 24, 2016

34 users found this comment helpful.
Did you? Yes  No  |  Report inappropriate

Page 1 2 3 4 5 Next
Hide