Would you have Constipation when you have Ankylosing spondylitis?
Summary: Constipation is found among people with Ankylosing spondylitis, especially people who are female, 50-59 old, also have Ankylosing spondylitis, and take medication Humira.
We study 86 people who have Constipation and Ankylosing spondylitis from FDA and social media. Find out below who they are, other conditions they have and drugs they take.
You are not alone: join a mobile support group for people who have Ankylosing spondylitis and Constipation >>>
Ankylosing spondylitis (type of arthritis affecting the spine) can be treated by Humira, Enbrel, Remicade, Sulfasalazine, Celebrex, Meloxicam. (latest reports from Ankylosing Spondylitis 21,228 patients)
Constipation has been reported by people with osteoporosis, pain, high blood pressure, depression, high blood cholesterol.(latest reports from Constipation 80,049 patients)
On Dec, 16, 2014: 86 people who have ankylosing spondylitis and Constipation are studied.
Gender of people who have ankylosing spondylitis and experienced Constipation * :
Age of people who have ankylosing spondylitis and experienced Constipation * :
Severity of the symptom * :
|least||moderate||severe||most severe |
Top co-existing conditions for these people * :
- Spondylitis (22 people, 25.58%)
- Pain (9 people, 10.47%)
- Arthritis (8 people, 9.30%)
- Depression (8 people, 9.30%)
- Hypothyroidism (8 people, 9.30%)
- Anxiety (5 people, 5.81%)
- Neuropathy peripheral (5 people, 5.81%)
- Blood cholesterol increased (5 people, 5.81%)
- Hypertension (4 people, 4.65%)
- Hypoaesthesia (3 people, 3.49%)
Most common drugs used by these people * :
- Humira (41 people, 47.67%)
- Enbrel (14 people, 16.28%)
- Remicade (12 people, 13.95%)
- Vioxx (9 people, 10.47%)
- Lyrica (6 people, 6.98%)
- Methotrexate (6 people, 6.98%)
- Cymbalta (5 people, 5.81%)
- Lorazepam (5 people, 5.81%)
- Simvastatin (5 people, 5.81%)
- Celebrex (4 people, 4.65%)
* Approximation only. Some reports may have incomplete information.
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.
Do you have Ankylosing Spondylitis and Constipation?
You are not alone! Join a mobile support group:
- support group for people who have Constipation and Ankylosing spondylitis
- support group for people who have Ankylosing spondylitis
- support group for people who have Constipation
Could your drug cause:
Other conditions that could cause:
Can you answer these questions (Ask a question):
- Cymbalta r/t autonomic neuropathy
losartan 20 mg
tired all the time, dizziness, chronic constipation, stomach pains, pins and needles, diabetic type 2 hx alcoholism resolved, gerd, early satiety
- Gastro with constipation in a 4 year old only cause pain at night?
In childrens hospital now have given the tag virus for stomach pain at night that is relieved by morphine
- Can my symptoms actually pinpoint a cause/condition? (1 answer)
I would just like insight on this. I'm on pain management right now, but it's just to manage the pain. Every thing else has really been not taken serious by any physican it office I've been to. Is this normal stuff many woman go through? I'm just sick of feeling like this between the constant pain & the daily having to pluck hairs it's insane. I'm in fantastic shape(used to be double my weight & now I'm 100lbs), the best looking I've ever been with a incredibly good looking husband & a wonderful family. My issues seem to detour a lot of things & while I'm young I'd like to get this solved or some type of solution to even maintain myself, not looking for a miracle, but would really appreciate answers.
- Has anybody had multi lobar pneumonia from reaction to methotrexate?
Bilateral multilobar pneumonia - rheumatologist considers it was caused by a reaction to methotrexate I was taking for ankylosing spondylitis and I was lucky to survive. Anyone have this and later shown to have scarring of the lungs?
- Has anyone had problems with blood work eg. elevated levels of lymphocytes?
Had further blood work done and nothing showed up? tested for viral infections mono hiv cmv toxoplasmosis all neg. surface immunophenotyping by flow cytometry done nothing there any answers here?
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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.
- I need advise, badly ckd!! (1 response)
The orthostatic BP started in mid April, I was only dizzy upon wakening then it would subside. I have never been a big breakfast eater so I started doing that. We were in Disney later in April and I was extremely fatigued, to the point of not wanting to walk, Disney would be the first time I passed out when getting dizzy. I of course said I had gotten too warm and was exhausted from work the previous week. The dizziness continued in the mornings & I passed out several more times. On May 1st, I passed out while putting my make-up on and hit my eye on the faucet and head on the tile floor, despite that I went to work thinking it would subside, it didn't. I went to the ER directly after work. They ran a B-met on me and my GFR was 11 and creatinine 3.95. They admitted me to a larger hospital for evaluation. While in there, they pumped me with fluids continuously, saying I had severe dehydration. My kidney function improved, my creatinine levels went back down to 1.34. After 5 days I was discharged and told to see a cardiologist and endo. The endo doc cancelled my appointment on the basis it was not his area. I had had a cortisol and ACTH testing which I guess was normal. I saw the cardiologist, who said it wasn't cardio. I had had an echocardiogram in the hospital and EKG monitoring. Cardio sent me to neurology, the PNRN did a basic neurological exam and drew blood for disease markers such as Lupus, sjorgens, hepatitis, ect. All disease markers came back negative, but my GFR was at 11 again and creatinine was 4.25, BUN 50 along with an elevated ACE level. They called me and said I sarcoidosis. I really don't have any of the primary S/S of this autoimmune disease. I don't know where to go from here, they are referring me to another neurologist at a bigger hospital. I can't live my normal life, can't walk on my feet due extreme pain and I pass out at least 2x a week, which is not good for my old body. My BP upon laying and sitting runs like 117/72, upon standing it drops to like 70/50-50/30. I am on 0.1 mg of florinef, I tried increasing it but then my legs swelled up for a gain of 23#. I talked to Mayo Clinic today and all there specialists are booked out thru December. I have to be able to work, I can't stay home any longer than September 8th! Please advise me!
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