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Would you have Rash (Rashes) when you have Ankylosing spondylitis?

Summary: Rash is found among people with Ankylosing spondylitis, especially people who are female, 40-49 old, also have Pain, and take medication Humira.

We study 624 people who have Rash (Rashes) 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 Rash >>>

 

 

 

 

Ankylosing spondylitis

Ankylosing spondylitis (type of arthritis affecting the spine) can be treated by Humira, Enbrel, Remicade, Sulfasalazine, Celebrex, Methotrexate. (latest reports from 21,242 Ankylosing Spondylitis patients)

Rash

Rash (redness) has been reported by people with rheumatoid arthritis, high blood pressure, high blood cholesterol, osteoporosis, depression. (latest reports from 150,999 Rash patients)

On Jan, 1, 2015: 631 people who have ankylosing spondylitis and Rash are studied.

Trend of Rash in ankylosing spondylitis reports

Gender of people who have ankylosing spondylitis and experienced Rash * :

FemaleMale
Rash52.11%47.89%

Age of people who have ankylosing spondylitis and experienced Rash * :

0-12-910-1920-2930-3940-4950-5960+
Rash0.00%0.00%1.68%11.07%18.96%20.64%27.35%20.30%

Severity of the symptom * :

leastmoderateseveremost severe
Rash25.00%75.00%0.00%0.00%

Top co-existing conditions for these people * :

  1. Pain (55 people, 8.72%)
  2. Spondylitis (44 people, 6.97%)
  3. Hypertension (38 people, 6.02%)
  4. Rheumatoid arthritis (27 people, 4.28%)
  5. Vitamin supplementation (27 people, 4.28%)
  6. Arthritis (26 people, 4.12%)
  7. Gastric disorder (23 people, 3.65%)
  8. Prophylaxis (22 people, 3.49%)
  9. Blood cholesterol increased (21 people, 3.33%)
  10. Hypothyroidism (20 people, 3.17%)

Most common drugs used by these people * :

  1. Humira (279 people, 44.22%)
  2. Enbrel (248 people, 39.30%)
  3. Remicade (181 people, 28.68%)
  4. Methotrexate (98 people, 15.53%)
  5. Sulfasalazine (58 people, 9.19%)
  6. Prednisolone (53 people, 8.40%)
  7. Folic acid (41 people, 6.50%)
  8. Prednisone (35 people, 5.55%)
  9. Omeprazole (34 people, 5.39%)
  10. Simponi (32 people, 5.07%)

* 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 Rash?

You are not alone! Join a mobile support group:
- support group for people who have Rash and Ankylosing spondylitis
- support group for people who have Ankylosing spondylitis
- support group for people who have Rash

Recent conversations of related support groups:

  • Support group for people who have Ankylosing spondylitis
    Hi everyone!!! I was diagnosed with AS 4 months ago after 9 months of waking up at 3am every morning with Thoracic stiffness and aches. A Rheumatologist diagnosed me and administered Humira. I have been pain free for 4 months.

Could your drug cause:

Other conditions that could cause:

Can you answer these questions (Ask a question):

  • How many/what percentage of older males who have had a stroke, have another while taking uloric?
    Concerned as my Rheumatologist wants me to start using Uloric40 mg and while I see that their is a relatively small incidence of stroke occurring (unless you are part of the "small" group); I have been unable to locate statistics for those previous stroke patients that are now using or have used Uloric, and had another stroke.
  • What drug helped most to get rid of rash?
    Antihistamines did not help my itchy rash from this drug. What else can I use or get from my doctor?
  • How long does redness last after picato?
    After 3 and a half weeks, I still have a huge red splotch on my face where I applied picato gel according to directions from my dermatologist. I'm very worried that it will be permanent. I had a huge water filled blister the morning after my first application of the gel. I used it two more times as directed. After a week, some of the redness was going away but I've seen no more improvement in the past two weeks. I'm still scaley, rough and red.

    Has anyone else experience this? I went by the doctors office the first morning and was told it was as expected. I've called back and been told not to worry. I see the dr in two more weeks, but for now, I'm quite upset that permanent damage has been done. I was not warned at all that this could happen. The photos in the medication packaging led me to believe that in 3 weeks, all redness would be gone. Info needed for sure. Please let me know. Thanks
  • I used coartem and developed redish all over my body. can coartem cause rashes
    i developed rashes which is itching me after using coartem for three days. also having sensation in my mouth and blister at the angle of my lips. could it be a side effect from coartem?
    pat
  • 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?

More questions for: Ankylosing spondylitis, Rash

You may be interested at these reviews (Write a review):

  • Pain meds that cause insomnia
    I currently take 7.5 mg of Vicoprofen for pain for my Anklyosing Spondylitis. I have tried Vicodin and Norco previously, but nothing worked as well as the Vicoprofen. I have never had to up my dosage and I am still getting the same level of relief as I was when I first started it over a year and a half ago. I swear by the Vicoprofen and would recommend it to anyone who has any type of related pain, but, there is one downfall. Every time I take my pain meds I get a huge burst of energy. My pain is usually worst at night, so I have no choice but to take it before bed. More times than not it causes me to suffer extreme insomnia, which is no fun. Up until recently I just suffered through it. I went and saw my primary today and told her about the issues and she suggested I try Trazodone to help ease my mind so I can fall asleep easier and faster. I'm really hoping it works because I don't want to have to switch pain meds because they work so well, but I can't go much longer only getting 2-3 hours of sleep during the week.
    I will wrote another review in a week or so regarding my experience taking the Trazodone with the Vicoprofen.
  • Lamotrigine severe rash
    I started taking 100mg of Teva-Lamotrigine Nov 22 once daily. I got a refill on Dec 5 that was Mylan-Lamotrigine. Two days later I woke up with an odd hot feeling rash all over my body and severe fatigue. I went back to bed 1/2 hour later after taking my regular Wellbutrin and the Lamotrigine. I woke up late morning. It got progressively worse during the day and I had a headache,fever and chills. I took the anti-histimine Aerius later that day which didn't help. The next day I went to a walk in clinic and they said it wasn't the Lamotrigine and thought it was a virus and did a throat swab. The fever and chills went away after a few days but I still have the rash. Finally after a week I saw a doctor that agreed it was the drug and I am now on the second week of Prednisone steroid treatment and prescription Reactin which is helping slowly. I have reported it to the Mylan drug company.
  • Rash from eating kale
    I ate kale for the first time on Monday. I only had a small bowl of fresh mixed green salad, so it wasn't entirely Kale. By Tuesday, I had a small rash on my left hip. I ignored it at first. Thursday evening, I decided to eat a large kale salad with other veggies and salmon, all of which I have eaten regularly aside from kale. Friday morning, my entire body was covered in the same rash that appeared Tuesday. I went to the ER. The doc said it was some type of allergic reaction. The ONLY thing I did/consumed different was the kale. I can't find much about it's reactions, though.
  • Humira: my experience
    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.
  • Skin rash in diclofenac potassium
    After a car accident in 2011 I took Diclofenac for back & shoulder off and on for about a year. During that time I developed random spots usually on my arms and legs that itch severely and sometimes get infected. I still suffer from the itchy spots and I am DESPERATE for a cure for my agony. I haven't taken the medicine for over a year but the itchy spots still come and go.

More reviews for: Ankylosing spondylitis, Rash

Comments from related studies:

  • From this study (3 months ago):

  • I HAVE HAD A PURITIC RED SPLOTCHY RASH OVER MOST OF MY BODY FOR THREE DAYS NOW. IT ITCHES SOME; BUT NOT SEVERELY. NO OTHER SIGNIFICANT SYMPTOMS.

    Reply

  • From this study (1 year ago):

  • Rash on upper thigh of right leg. Area approx 75 sq. cm.

    Reply

  • From this study (4 years ago):

  • Methotrexate was added to manage the undesired antibody reaction. This seems to help some.

    Reply

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