Trigger finger is found among people with Osteoarthritis, especially for people who are female, 60+ old, take medication Vioxx and have Osteoporosis. We study 31 people who have Trigger finger and Osteoarthritis from FDA and social media. Find out below who they are, other conditions they have and drugs they take.
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Osteoarthritis (a joint disease caused by cartilage loss in a joint) can be treated by Celebrex, Meloxicam, Mobic, Naproxen, Tramadol (latest reports from 46,411 Osteoarthritis patients)
Trigger finger has been reported by people with muscle aches, rashes, osteoporosis, speech impairment (adult), hypersensitivity (latest reports from 1,987 Trigger finger patients).
On Sep, 17, 2016
31 people who have Osteoarthritis and Trigger Finger are studied.
* Approximation only. Some reports may have incomplete information.
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I was diagnosed with MS in 1997. My right arm, shoulder and hand have recently become involved. (In the last couple of years). Before this, it was just my balance, spasticity in my legs and numbness and tingling in my legs that were involved. Now I suddenly have trigger finger in my left hand ring finger. I'm trying to figure out if it is related to the MS, or something I should see a different doctor for.
Hello Everyone, I have never been in a group and written my words down like this before, for all to see. . So, I am not sure what I will say. I can tell you I have been on methadone for 23 years,( I HATE IT!!!) and I indeed have degenerative joint disease, as well as degenerative disc disease and scoliosis, stenosis, my shoulder, hips, knees, wrists are all messed up and now, a MRI of my neck. I know I worked very all my work life, but, something is up. And I am really worried and scared for myself. "Humana". They really don't care if I live or die. Either does Medicare. It is very depressing, the insurance. The doctors the pharma corporations and insurance companies are all in bed together. That is why it is proclaimed, the Medicare system is BROKEN AND CORRUPT!!! But, back to the methadone they so freely prescribe. I do believe the methadone is eating my bones away. When I have asked the doctors, they just deny any bone degeneration from the methadone. For years, they have denied that. They are all in the same boat and the doctors, are all indoctrinated. Which, of course, they don't want to hear, at all. I don't know what to do about my bones. I have told my doctor that it feels like I have Bone Cancer. Her response was, my BLOOD doesn't show any cancer. I do have osteoporosis, big time. They just think THEY DO NO HARM I did not think I would write this long. I am so sorry for all of you that are suffering. AND, possibly, Needlessly. I hate to see anybody suffer, it bothers me....deep. So, this is my introduction....... Hello to all my fellow suffers....I wish you well, I wish you better. Bye, Marilyn I am hesitant to click that button......."Join the group" Never joined a group before. So........Here goes............
HI my name is Deb. i just turned 50 in july and have been taking Tegretol since age 9 for Epilepsy. I was just diagnosed with severe osteoarthritis and need a total hip replacement much to the surprise of myself and my doctor. After reading about osteoarthritis on the Internet is am thinking ...
I have been on several meds for years. The ones listed and a few others, Prednisone, Carbidopa-leva, Colcrys, Celebrex. I was started on Folic Acid and Sulfasalazine in Aug 2015 for the Rheumatoid factor discovered in a routine blood test. I've had the same doctors for years, General ...
Hi, I'm Mike, I'm 66 and need to do something about right hip and knee. As a horse trainer I've used pentosan injections on my horses for years with good results - was wondering if there's an official way for me to get it for myself.
Hello Everyone, I have never been in a group and written my words down like this before, for all to see. . So, I am not sure what I will say. I can tell you I have been on methadone for 23 years,( I HATE IT!!!) and I indeed have degenerative joint disease, as well as degenerative disc ...
I was diagnosed with MS in 1997. My right arm, shoulder and hand have recently become involved. (In the last couple of years). Before this, it was just my balance, spasticity in my legs and numbness and tingling in my legs that were involved. Now I suddenly have trigger finger in my left ...
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