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Would you have Ringing in the ears (Tinnitus) when you have Rheumatoid arthritis?





Summary: Ringing in the ears is found among people with Rheumatoid arthritis, especially people who are female, 60+ old, also have Hypothyroidism, and take medication Methotrexate.

We study 406 people who have Ringing in the ears (Tinnitus) and Rheumatoid arthritis 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 Rheumatoid arthritis and Ringing in the ears >>>

Rheumatoid arthritis

Rheumatoid arthritis (a chronic progressive disease causing inflammation in the joints) can be treated by Methotrexate Sodium, Methotrexate, Enbrel, Humira, Prednisone, Plaquenil. (latest reports from Rheumatoid Arthritis 218,505 patients)

Ringing in the ears

Ringing in the ears (a ringing in the ears) has been reported by people with depression, high blood pressure, osteoporosis, high blood cholesterol, stress and anxiety.(latest reports from Ringing in the ears 19,199 patients)

On Nov, 25, 2014: 406 people who have rheumatoid arthritis and Ringing In The Ears are studied.

Trend of Ringing in the ears in rheumatoid arthritis reports

Gender of people who have rheumatoid arthritis and experienced Ringing in the ears * :

FemaleMale
Ringing in the ears83.93%16.07%

Age of people who have rheumatoid arthritis and experienced Ringing in the ears * :

0-12-910-1920-2930-3940-4950-5960+
Ringing in the ears0.00%0.00%0.00%1.75%3.71%20.74%28.38%45.41%

Severity of the symptom * :

leastmoderateseveremost severe
Ringing in the ears0.00%60.00%26.67%13.33%

Top co-existing conditions for these people * :

  1. Hypothyroidism (78 people, 19.21%)
  2. Osteoporosis (73 people, 17.98%)
  3. Hypertension (46 people, 11.33%)
  4. Ulcer (32 people, 7.88%)
  5. Diabetes mellitus (27 people, 6.65%)
  6. Pain (22 people, 5.42%)
  7. Vitamin supplementation (20 people, 4.93%)
  8. Folate deficiency (14 people, 3.45%)
  9. Gastrooesophageal reflux disease (13 people, 3.20%)
  10. Gastric disorder (13 people, 3.20%)

Most common drugs used by these people * :

  1. Methotrexate (219 people, 53.94%)
  2. Enbrel (194 people, 47.78%)
  3. Humira (178 people, 43.84%)
  4. Folic acid (123 people, 30.30%)
  5. Fosamax (96 people, 23.65%)
  6. Remicade (78 people, 19.21%)
  7. Synthroid (61 people, 15.02%)
  8. Prednisone (46 people, 11.33%)
  9. Omeprazole (45 people, 11.08%)
  10. Plaquenil (43 people, 10.59%)

* Approximation only. Some reports may have incomplete information.

Comments for this study:

ArnieK (12 months ago):

Trying to find an anti inflammatory medicine for arthritis ( using Arthrotec ) that does not worsen tinititus.
Reply the comment

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 Rheumatoid Arthritis and Ringing In The Ears?

You are not alone! Join a mobile support group:
- support group for people who have Ringing In The Ears and Rheumatoid arthritis
- support group for people who have Rheumatoid arthritis
- support group for people who have Ringing In The Ears

Could your drug cause:

Other conditions that could cause:

Can you answer these questions (Ask a question):

  • I have ringing in the ears. is there anyway of getting rid of it?
    I feel this tinnitus was induced from my taking the norgesic forte, that I no longer take for tension headaches. But I do take over the counter aspirin. Can the tinnitus ever go away?
    Reply
  • What side effects do you experience from sulpfasalazine? (3 answers)
    I began taking sulfasalazine 5 days ago for Rheumatoid arthritis. Since then I've had stomach cramps and bloating. Has anyone else experienced these side effects? If so, did the symptoms go away after using taking the meds for a while? And did the meds help the RA symptoms?
    Reply
  • Nimotop for curing tinnitus?
    i have tinnitus and the doctor is giving me nimotop 30 mg is this good?
    Reply
  • Is there a support group in the us for people with insulinomas? (1 answer)
    SUPPORT GROUP IN UNITED STATES!!!

    Hi, the only support group that I've been able to find for people with insulinomas is located in the UK... just wondering if there is one in the US. I had pancreatic surgery to remove my first insulinoma in 2012, we're thinking there's another because I'm still having problems with hypoglycemia... if anyone know anything, PLEASE CONTACT ME!!! :)
    I know there can't just be a support group here for FERRETS!!! people are kind of important... I hate this song, but "Don't worry, BE HAPPY" is okay, I guess... I'm trying to force it upon myself. Things will get BETTER!!!
    Reply
  • Can this medication cause the ears to ring?
    I developed tinnitus about one year ago. I understand that there is no cure for it. I'm researching it myself. I'm also in a research program that requires me to wear small ear generators. It doesn't seem to help at this time.
    Reply

More questions for: Rheumatoid arthritis, Ringing in the ears

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

  • Ringing in the ears from linzess
    I started Linzess about a month ago, taking it about every three days. It was my miracle pill, until recently when I started having ringing in my ears. I am stopping the medication in hopes that the ringing will subside.
    Reply
  • Side effects of using terazosin
    I have been on terazosin for 9 days. The ringing in my ears is unbearable, dizzy in the night if I wake up to use the bathroom, intermittent throbbing heartbeat. Also very significant is dramatic decrease in libido and difficulty achieving satisfaction. Dose started at 5 mg at night, reduced to 2 mg. at night after two days and ringing does not go away. I have permission from my doctor to discontinue use and replace with Lisinopril.
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  • Why has my bloodpresher now shot up
    My blood pressure was always low 120/68 now since being treated for rheumatoid arthritis it has shot up to 175/92
    Reply
  • Had nms in 2005, will trileptal increase chance of recurrence?
    In 2005 I had NMS, which was not detected by my drs for 4 months. I'd been on Lexapro & Seroquel for 2 yrs, but was weaned from Lexapro & placed on Lamictal 3/05. Began getting low-grade fevers, which I was told were not caused by the Lamictal. I quit taking it anyway, fevers (along with uncontrollable shivering) continued & got higher. By 5/05 my temps were reaching 105 deg F. Husband said I became combative, refused to go to hospital. Early June/05 he came home to find me wrapped in blankets, with a temp over 105 F. He tried to place me in a tub of cold water, said I was rigid & screamed when he tried to move me. I was in the tub, speaking "in tongues" (his description, I have no memory of this). He called 911, took me to hospital. I woke, no idea where I was or why. After a lumbar puncture & 2 days in ICU I went home. The fevers continued...2 weeks later he came home to find me wrapped in sheets, towels, blankets, with the heat on full (it was in the 90's outside) he called ambulance again. I awoke to find myself under an ice blanket with nurses pushing large vials of dantrolene into both arms, several liters. Another LP, a stint in ICU...this time they told me it was NMS. The dr who dxd me said he was surprised I was alive, & not a vegetable, as my temp had peaked at 109 deg F. I suffered brain damage; short-term memory loss, brain can't control my body temp, my blood pressure went up. An arteriogram showed completely healthy heart & arteries, no plaque at all. I lost all body fat as well as some muscle mass. The fevers continued even after stopping the Seroquel. I visited my PCP for a checkup in 9/05, temp was normal. I started shuddering, my temp went up a full degree every 5 minutes. PCP admitted me to ER, my heart rate was over 272 B/M; they stopped my heart 3 times to "reset" it, which didn't work. I spent 3 days in hospital. Several months later my P doc tried me on Lamictal alone; I got Stevens-Johnson syndrome. I stopped the drug as soon as the signs appeared. I've been untreated, except for Neurontin & Primidone, until my manic episodes became unlivable. 3 weeks ago I went 8 days with no sleep, became psychotic. My P doc gave me Trileptal, which has evened my moods, but I've been getting low-grade fevers (highest was 103.6). Would having had NMS in the past make me more prone to falling to it again with the Trileptal? It's the only new med I've taken in over a year.
    Reply
  • Still ill after several years (1 response)
    I became ill several years ago.
    It all started with a head cold that lasted a few months and left me with Tinnitus and chronic sinusitis.

    After a nose operation and many visits to the doc and hospital, I am no closer to felling better or being cured.
    My doc gave me Beconase Aq at first and this made me very unwell, causing me fatigue which would last for a few days. I'm still searching for help.
    Reply

More reviews for: Rheumatoid arthritis, Ringing in the ears

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