Review: could Humira cause Numbness and tingling?
Summary: Numbness and tingling is found among people who take Humira, especially for people who are female, 40-49 old, have been taking the drug for 2 - 5 years, also take medication Methotrexate, and have Rheumatoid arthritis.
We study 136,021 people who have side effects while taking Humira from FDA and social media. Among them, 64 have Numbness and tingling. Find out below who they are, when they have Numbness and tingling and more.
You are not alone: join a mobile support group for people who take Humira and have Numbness and tingling >>>
Humira has active ingredients of adalimumab. It is often used in rheumatoid arthritis. (latest outcomes from 136,734 Humira users)
Numbness and tingling
Numbness and tingling (unusual prickling sensations) has been reported by people with high blood pressure, depression, pain, multiple sclerosis, high blood cholesterol. (latest reports from 4,981 Numbness and tingling patients)
On Feb, 3, 2015: 136,006 people reported to have side effects when taking Humira. Among them, 64 people (0.05%) have Numbness And Tingling.
Time on Humira when people have Numbness and tingling * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
|Numbness and tingling||12.90%||19.35%||16.13%||16.13%||32.26%||3.23%||0.00% |
Gender of people who have Numbness and tingling when taking Humira * :
|Numbness and tingling||66.67%||33.33% |
Age of people who have Numbness and tingling when taking Humira * :
|Numbness and tingling||0.00%||0.00%||6.67%||8.33%||10.00%||28.33%||21.67%||25.00% |
Severity of Numbness and tingling when taking Humira ** :
|least||moderate||severe||most severe |
|Numbness and tingling||0.00%||100.00%||0.00%||0.00% |
How people recovered from Numbness and tingling ** :
|while on the drug||after off the drug||not yet |
|Numbness and tingling||0.00%||0.00%||100.00% |
Top conditions involved for these people * :
- Rheumatoid arthritis (23 people, 35.94%)
- Crohn's disease (21 people, 32.81%)
- Ankylosing spondylitis (13 people, 20.31%)
- Psoriasis (9 people, 14.06%)
- Psoriatic arthropathy (9 people, 14.06%)
Top co-used drugs for these people * :
- Methotrexate (20 people, 31.25%)
- Folic acid (14 people, 21.88%)
- Zyrtec (9 people, 14.06%)
- Prednisolone (7 people, 10.94%)
- Ramipril (6 people, 9.38%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
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Drugs in real world that are associated with:
Could your condition cause:
Can you answer these questions (Ask a question):
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- Does humira cause bad common warts and how to get rid of them, tried dcp treatment, still the same
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More questions for: Humira, Numbness and tingling
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I have had some form of arthritis probably since birth. My father and maternal grandfather had some form of arthritis. I began to realize pain in both ankles if I stood or walked too long.
I began taking many NSAIDs when I was around 22. I've done gold, prednisone (twice), plaquenil, butazoidin, sulfasalazine, etc. My best results came with methotrexate after I got cellulitis in my knee (scratch it while kayaking in the summer, fiberglass boat). It dropped my sed rate from over 100 to 35 or so within a few months. I continued with MTX from 1977 to 2000 when my MD suggested Enbrel and stopping MTX. That was a VERY bad decision. Enbrel appeared to mask the disease for a few years. I had my left MCP replaced in 2004, my right heel debrided in 2010, and both my TMJs replaced in 2012. I strongly believe that if I had kept with the MTX it would have delayed those changes. Additionally, in 2011 I was in a bus crash returning from RAGBRAI. I got knocked out from three to six minutes. I had a nasty concussion that lasted 2+ years. Towards the end of the third year post accident I started exercising more aggressively. After doing several 40, 50, and 60 miles rides, I took a leisurely 50 mile ride around Boston at night. Two days later I had a spinal edema. So much for biking and other active sports! :-(
I have continued with MTX. Late 2013 my MD increased my MTX to .8/week. I had been taking .6/week. I stopped taking Enbrel and switched to Humira in early 2014. I took it for a few months before my doc and I realized it was not doing any better than Enbrel. I tried Humira for three months but it did not seem to work any better than Enbrel. In early June I stopped Humira and waited a few weeks before I started Otezla. I stopped Oterzla on 9/15/14 because it made me depressed and allowed my morning stiffness to get much worse.
I started prednisone again from the start of July. By mid-August I told my MD that I was screaming louder than I ever had; my dog was very startled. I stopped it gradually over the next two weeks. Meanwhile, the Otezla made me feel awful.
My MD is going to get me onto another injectable that I take monthly. I forget its name.
- Reaction to methylpred
I have a severe case of poison ivy for which I was given Prednisone. Still suffering 1 week later went back to doctor (was at 2x/day at that point) and was then put on methylpred 4mg PAK. Today is my second day on this. First noted tingling on my insides in my trunk area this morning, later in arms and hands and numbness in my tongue. Weird internal feeling. Now I itch and tingle.
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Comments from related studies:
From this study (1 year ago):
Items in section 3 are currently under evaluation. Most began to emerge, subtly, approximately 11 years ago and have intensified over the past 2-3 years. Myelomalacia involving a 9.5-cm segment of the posterior column of the spinal cord was demonstrated on MRI 2 weeks ago.
NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.
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