Review: could Metformin cause Joint pain?
Summary: Joint pain is found among people who take Metformin, especially for people who are female, 60+ old, have been taking the drug for 2 - 5 years, also take medication Metformin hcl, and have Diabetes.
We study 97,426 people who have side effects while taking Metformin from FDA and social media. Among them, 1,802 have Joint pain. Find out below who they are, when they have Joint pain and more.
You are not alone: join a mobile support group for people who take Metformin and have Joint pain >>>
Metformin has active ingredients of metformin hydrochloride. It is often used in type 2 diabetes. (latest outcomes from 100,962 Metformin users)
Joint pain has been reported by people with rheumatoid arthritis, osteoporosis, high blood cholesterol, high blood pressure, multiple sclerosis. (latest reports from 118,740 Joint pain patients)
On Jan, 26, 2015: 97,426 people reported to have side effects when taking Metformin. Among them, 1,802 people (1.85%) have Joint Pain.
Time on Metformin when people have Joint pain * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
|Joint pain||16.39%||22.95%||9.84%||3.28%||24.59%||19.67%||3.28% |
Gender of people who have Joint pain when taking Metformin * :
|Joint pain||62.14%||37.86% |
Age of people who have Joint pain when taking Metformin * :
|Joint pain||0.13%||0.00%||0.46%||0.92%||4.60%||14.53%||29.13%||50.23% |
Severity of Joint pain when taking Metformin ** :
|least||moderate||severe||most severe |
|Joint pain||0.00%||58.33%||36.11%||5.56% |
How people recovered from Joint pain ** :
|while on the drug||after off the drug||not yet |
|Joint pain||0.00%||0.00%||100.00% |
Top conditions involved for these people * :
- Diabetes mellitus (349 people, 19.37%)
- Hypertension (230 people, 12.76%)
- Type 2 diabetes mellitus (188 people, 10.43%)
- Rheumatoid arthritis (163 people, 9.05%)
- Depression (152 people, 8.44%)
Top co-used drugs for these people * :
- Metformin hcl (1,093 people, 60.65%)
- Aspirin (455 people, 25.25%)
- Lisinopril (301 people, 16.70%)
- Lipitor (228 people, 12.65%)
- Simvastatin (225 people, 12.49%)
* 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.
Do you have Joint Pain while taking Metformin?
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- support group for people who take Metformin and have Joint Pain
- support group for people who take Metformin
- support group for people who have Joint Pain
Drugs in real world that are associated with:
Could your condition cause:
Can you answer these questions (Ask a question):
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Just curious, but when you have a reaction to a medicine, who is responsible for reporting it to the manufacturer of the drug?
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I am feeling weak, out of breath, and have difficulty walking due to my swelling, achiness, and slight pain! I was feeling fine just a few weeks ago......... had traveled and had no complaints........
- 2 weeks after septoplasty, inside of middle/upper nose burns-why?
The diabetes was diagnosed about 5 yrs. ago. On prednisone for a psuedotumor. Surgeon went little bit into sinuses to cut a piece of bone. That was to help drain sinuses; chronic infections and suspected link to psuedotumors. Probably blew nose sooner than recommended; clotting made difficult to breath. What's recommended to relieve that sort of pain?
- I had bladder cancer and my doctor put me on metformin should i get off this
I do not want to take this metformin if it may cause my bladder cancer to come badk
- I have been told by my gastroenterologist that i have gastroparesis, what are my treatment options, if any?
I've had a CT scan and a Gastric Emptying study completed. My stomach is only 35% emptied after 4 hours, it should be at least 90% empty at that point. I have a colonoscopy and esophagealendoscopy scheduled for the first week of the year. What are my treatment options at this point?
More questions for: Metformin, Joint pain
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Comments from related studies:
From this study (3 months ago):
Naprosyn, Vicodin, Ativan and Prilosec are taken only on an as needed basis. Some of my symptoms are intermittent, and some are chronic. The though the medications may not completely rid me of a symptom (for example, depression or muscle pain), they do improve my condition enough to warrant their continued use. I'm much better off taking them than not.
The oral issues I'm having all began around the same time in the last year. I first noticed a sensitivity for spicy food I had never experienced. I can no longer use adult toothpaste because the minty flavors are so provinces as to cause pain. The gum irritation comes and goes as does the severity of the other oral pain I experience.
My hair loss I can describe as severe as it can be without having visible bald spots. Whereas I once had unusually thick hair (a ponytail of around 1.5 inches), I have lost so much that my ponytail now measures about .5 inches.
Sumac on Oct, 24, 2014:
I think a lot of you have disseminated histoplasmosis. Histoplasmosis is carried by bats.
From this study (6 months ago):
I've been diagnosed with sero-negative rheumatoid arthritis. I have only tested minimally positive on the anti-CCP test and had a slightly high SED rate. My most recent tests showed some slight elevation in some RA marker tests, but nothing really significant. My rheumatologist is now doubting whether I have RA or some other pain syndrome going on.
IHateRA on Jul, 22, 2014:
My first RA Dr. put me on Plaquenil, it seemed to work for six months, then stopped - I thought the dose would be adjusted but it wasn't, so I went to another RA Doc - C-RP wasn't too high, sero neg. Was put on methotrexate - I ended up with a mouth sore the NEXT day, then bumps started appearing on my face, like zits, but NOT zits. I didn't touch them, but they ulcerated, left me full of scars on face, legs, etc - I have been OFF methotrexate for 5 years AND still have the same problem along with a daily fever (100+) and severe sweating - I knew the bumps were a sign of being allergic to Methotrexate, I quit it right away, called Dr. to get in - they told me 3 months (I was an established patient). In terms of fever and sweating, the ONLY thing I have in common with some of these posts and drug lists is METHOTREXATE - I wouldn't allow a pet to take it. I seem to have more in common with a friend who as MS - but my reg. doc doesn't listen to that. I can't take bio. drugs (live in "fungal" region), so I take pain medicine - as little as possible, I guess the Methotrexate is STILL messing with my body. I have a very good acupuncturist - when I told him that my Doc. wasn't "sure" about RA, he poked me (lightly) with his finger in two places and ask which hurt more. He confirmed the RA as it travels on certain meridians in Chinese medicine. Had I picked a different spot for hurting more, then we would have to figure out what I really had. My joints are deteriorating but now I'm afraid of the drugs for RA, so I just put up with and manage the pain (which is extreme) with pain meds, cold therapy (I love my cryo-cuff), and acupuncture. I wish that the side effects of RA drugs weren't as bad as they are! Leaving Cymbalta, Lyrica, Plaquenil and Methotrexate (all at different times) OUT of my body made me realize that they did affect me - I was "foggy" and sluggish mentally but didn't really notice it until I quit them.
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