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Real members of myRAteam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.

I Have A Question On Medications.

I Have A Question On Medications.

I’ve been diagnosed with RA 5 months ago. I’m currently taking Avara and Medrol, have been on these two meds since diagnosed with RA. My rheumatologist is tapering me off of the Medrol. On top of Avara, she’s proposing to add Humira and INH for 9 months to my treatment. Because I have a positive TB skin test. I would need to take INH with Humira. Anyone out there taking these medications, anything I should know about them such as major side effects and what to look out for. Is Humira effective… read more

posted March 4, 2021
A myRAteam Member

Humira worked well for me for 10 years, BUT people react differently to meds. Be open to trying several to find relief. Frustrating but necessary. You will know when you find one that works.

posted March 7, 2021
A myRAteam Member

I do not and have never taken Humira, I take Enbrel. I have done it with a needle, a pen and now I take the mini's with a little machine kind of thing. It is hand held. I was diagnosed in October 2015. It was the first biologic and the only one I have ever taken. I am in remission and I am praying it continues. One reason, is because they have a wonderful foundation that pays for it for me. It is approximately $1000.00 per week. You take one shot a week. That adds up fast. I have never paid for it. So, I have been fortunate.

You may ask why did you even comment if you don't use Humira?? Well, it is not because of the medication or how you take it. What I wanted to talk about was how fortunate you are to have an RA doctor that seems so willing to change when something is not working or whatever. May RA doctors are very slow to get you started on some meds and then they are very slow to change your med, unless there is an obvious allergic reaction. I love my RA doctor, she is wonderful, She picked the right medication right away, she helped me and coached me through getting on disability after telling I can not work anymore. I got it the first time. I am very thankful, but I also some nightmares from some RA patients, when they can't get it, or it takes all day, or they drive a bunch of miles. So, I rejoice with you that you have a very attentive and quick working doctor. When they are proactive the way you described, you get settled on the right medication and usually are able to stay on it short term. May God bless you on your journey.

posted May 22
A myRAteam Member

Humira was not strong enough for me and I believe it taps after so long. I had site injection reaction with Humira with hives as big as silver dollars, was told to take benedryl day before, day of and day after, not for me, so I am now on Symponi.

posted March 8, 2021
A myRAteam Member

Yes I also inject myself. I've been on it for about 10 years now and it's been keeping my arthritis stable. I have a lot of bone deterioration mainly because I've had arthritis so long that it's had a field day.

posted March 4, 2021
A myRAteam Member

The first time I used the Humira pen I had it backwards and injected it into my thumb. It did work well for me about 7 years. Then, unfortunately I became allergic to it. This has happened to me so many times over the past 22 years that I rely on my rheumatologist to tell me now what I have had and what I am allergic to…

posted December 25, 2021

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