Tendonitis is found among people who take Magnesium Oxide, especially for people who are male, 60+ old also take medication Zometa, and have Breast cancer metastatic . We study 4,634 people who have side effects while taking Magnesium oxide from FDA and social media. Among them, 30 have Tendonitis. Find out below who they are, when they have Tendonitis and more.
On eHealthMe you can find out what patients like me (same gender, age) reported their drugs and conditions on FDA and social media since 1977. Our tools are free and anonymous. 86 million people have used us. 300+ peer-reviewed medical journals have referenced our original studies. Start now >>>
Magnesium oxide has active ingredients of magnesium. It is often used in constipation. (latest outcomes from Magnesium oxide 4,679 users)
Tendonitis (a condition that causes pain and swelling of tendons) has been reported by people with breathing difficulty, rashes, itching, stroke, chest pain (latest reports from 9,174 Tendonitis patients).
On Jul, 23, 2016
4,634 people reported to have side effects when taking Magnesium Oxide.
Among them, 30 people (0.65%) have Tendonitis
* 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.
Hi. I am curious to hear what your experience with tendon issues was when taking Atripla. The last 3 years I have had major issues with my feet. My tendon weakened and eventually caused my arch to collapse of one foot. I then had issues with the other foot where I had plantar faciatis, posterior tibial tendonitis, and then achilles tendonitis. I had a calcification form on the back of my heel bone and this has caused my achilles tendon to tear. I am having trouble with my knees recently and have most recently felt pain in my joints in my hands. My HIV doctor was curious to possibly take me off Atripla and start me on another drug but was not sure if the Atripla was the cause of all my tendon issues. Can anyone share any information about the pain you have and if you have stopped taking Atripla and things improved? Thanks so much.
I've been on Imuran for my Crohns Disease for over 20.years, I have AVN in both hips (5 hip replacements) I had the Depuy Metal on Metal Pinnacle Cup components. Got Melatosis and had revisions done on both hips, replaced with ceramic femoral heads and plastic lining in the cup. My left hip ...
Hi. I am curious to hear what your experience with tendon issues was when taking Atripla. The last 3 years I have had major issues with my feet. My tendon weakened and eventually caused my arch to collapse of one foot. I then had issues with the other foot where I had plantar faciatis, ...
I have used Zolpidem since 1998 with sporadic breaks from the drug. Over the years I've noticed side effects that aren't listed anywhere but disappeared when I stopped using the drug. About ten years ago my hands hurt so badly that I was afraid to shake hands with anyone and the little finger ...
I have taken 4 shots and after the last two, I have shoulder pain and tendinitis, with pain shooting down my arm. I am going to physical therapy, which has helped a little, but my arm and hand feel numb when I get up in the morning. Could this be caused by Prolia?
NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.
WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.
DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.
You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.