Review: could Multivitamin cause Bone and joint pain (Joint pain)?
Summary: Bone and joint pain is found among people who take Multivitamin, especially for people who are female, 60+ old, have been taking the drug for 2 - 5 years, also take medication Aspirin, and have High blood pressure.
We study 7,900 people who have side effects while taking Multivitamin from FDA and social media. Among them, 422 have Bone and joint pain. Find out below who they are, when they have Bone and joint pain and more.
You are not alone: join a mobile support group for people who take Multivitamin and have Bone and joint pain >>>
Multivitamin has active ingredients of ascorbic acid; biotin; cyanocobalamin; dexpanthenol; ergocalciferol; folic acid; niacinamide; pyridoxine hydrochloride; riboflavin phosphate sodium; thiamine hydrochloride; vitamin a; vitamin e. It is often used in vitamin supplementation. (latest outcomes from 9,004 Multivitamin users)
Bone and joint pain
Bone and joint pain has been reported by people with rheumatoid arthritis, osteoporosis, high blood cholesterol, high blood pressure, multiple sclerosis. (latest reports from 118,740 Bone and joint pain patients)
On Jan, 27, 2015: 7,900 people reported to have side effects when taking Multivitamin. Among them, 422 people (5.34%) have Bone And Joint Pain.
Time on Multivitamin when people have Bone and joint pain * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
|Bone and joint pain||0.00%||21.43%||7.14%||3.57%||32.14%||14.29%||21.43% |
Age of people who have Bone and joint pain when taking Multivitamin * :
|Bone and joint pain||0.00%||0.00%||1.99%||1.74%||8.21%||16.92%||20.40%||50.75% |
Severity of Bone and joint pain when taking Multivitamin ** :
|least||moderate||severe||most severe |
|Bone and joint pain||0.00%||38.71%||54.84%||6.45% |
How people recovered from Bone and joint pain ** :
|while on the drug||after off the drug||not yet |
|Bone and joint pain||10.00%||5.00%||85.00% |
Top conditions involved for these people * :
- Hypertension (48 people, 11.37%)
- Osteoporosis (43 people, 10.19%)
- Metastases to bone (42 people, 9.95%)
- Rheumatoid arthritis (39 people, 9.24%)
- Anxiety (37 people, 8.77%)
Top co-used drugs for these people * :
- Aspirin (134 people, 31.75%)
- Zometa (121 people, 28.67%)
- Vitamin d (95 people, 22.51%)
- Folic acid (79 people, 18.72%)
- Lipitor (75 people, 17.77%)
* 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 Bone And Joint Pain while taking Multivitamin?
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- support group for people who have Bone And Joint Pain
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- Faslodex driven hell
I have metastatic breast cancer...which has spread to my bones. Needless to say...I'm not a happy camper. Faslodex was my oncologist’s drug of choice for me. I've been on it since July 28, 2014....My first month was loading dosage...and each month that has followed I receive two injections in my tush...250mg each...for a total of 500mg monthly. Tomorrow, Monday November 17, 2014, will be my third round...not including the month of loading. As per my PET scan one month ago...the Faslodex has not started working. From everything I have been told...and read...it takes four to even six rounds to start working...if in fact it works at all.....@%^&*@#...says it all...if ya know what I mean.
What has kicked in from Faslodex...are some horrific side effects......About a month ago...I started having a strange little cough...dry...most of the time.....At times the cough becomes uncontrollable for aprox 15 / 20 minutes...then calms. NOTHING works at relieving it...although I suck down water like it is my last drink on earth...and use a wonderful...soothing throat drop, Halls Breezers...Cool Berry...which eases me...even if it is only psychologically, it is magical. The cough has gotten considerably worse over time...and for those that don't know me...I am sure they think I smoke ten packs a day. My voice is also affected at times due to the cough. My breathing is horrific...and I can no longer walk for any length of time...or for more than a short distance.....Nor can I walk and talk without coughing...and or losing my breath. Stamina...this I have none of!!! And this past week...the shit hit the fan.....Joining the cough...are bone and joint pains...as well as muscle pain. When I called my doctor...@ Sloan Kettering...I spoke with the nurse...and she had not a damn clue as to what might help. As a matter of fact...she told me that she has never heard of any of the side effects that I am now having. WHAT'S WRONG WITH THIS PICTURE???? EVERYTHING!!! However...when I check reputable sites...I find not a few...but hundreds of other people with the same side effects.
From what I have read on all the sites...the only way "WE" are going to get help with issues like these...is by sharing with one another. Not one of the individuals that I speak of has had any positive help with their side effects from their doctors. Am I pissed off??? You bet I am. As for depression...that only comes in small doses for me.....like yesterday...when my body hurt me so badly...my cough was out of control...I had difficulty breathing...and I could not stand on my own two feet without holding on. That moment in time has passed...but for how long??? What will I be hit with next??? When???
- Cymbalta caused joint pain
I had taken Cymbalta for about 1.5 years and after taking it for a few months, I started having widespread joint pain. The joint pain has gotten worse and is becoming debilitating. Joint pain in the literature as a side affect of the drug but the joint pain seems to be permanent! I have not taken Cymbalta in a couple years but the joint pain has remained. I have had blood tests and my doctor says the tests show it is not arthritis.
- Xylitol caused joint pain
For over a year I was chewing nicotine gum with xylitol. During that period I developed worsening joint pain to the stage where I was diagnosed with fybromyalgia (there was no other explanation for the pain). The chemist changed the brand of 2mg gum and I instantly felt better chewing it. After a week of feeling great I investigated what was missing in the new gum ( which was much less sweet) and it was xylitol. If I chew two or three pieces with it I begin to ache ( as an experiment done once)
I wanted to share this for ianyone else out there chewing gum and experiencing chronic pain. And yes, I know it should have got off the nicotine by now!
- 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.
- Xanax bed wetting will it stop and do i wear diapers or die (1 response)
I am on the very edge of crazy. So starting this is pushing ne way over. I'm 49 for crap sakes. I am so tired of the pain in my body and I am just tired, this is the last slap I can't anymore. Naturally alcohol I am sure is just about the end game along with cuts.
Just want to bleed out and not hurt anymore and be so scared to leave my house or sleep. I just want to sleep forever.
More reviews for: Multivitamin, Bone and joint pain
Comments from related studies:
From this study (3 weeks ago):
I did one shot in 2006. Horrible pelvic pain. My joints still hurt all over, 8 years later. I have synocope issues and migraines. This is like poison and should not be given to women.
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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