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Review: could Arixtra cause Osteoporosis?
We study 6,325 people who have side effects while taking Arixtra from FDA and social media. Among them, 3 have Osteoporosis. Find out below who they are, when they have Osteoporosis and more.
Get connected: join a mobile support group for people who take Arixtra and have Osteoporosis >>>
Arixtra (latest outcomes from 6,359 users) has active ingredients of fondaparinux sodium. It is often used in deep venous thrombosis.
Osteoporosis (bones weak and more likely to break) (latest reports from 216,747 patients) has been reported by people with osteopenia, high blood pressure, rheumatoid arthritis, pain, high blood cholesterol.
On Oct, 22, 2014: 6,325 people reported to have side effects when taking Arixtra. Among them, 3 people (0.05%) have Osteoporosis.
Time on Arixtra when people have Osteoporosis * :
Gender of people who have Osteoporosis when taking Arixtra * :
Age of people who have Osteoporosis when taking Arixtra * :
Severity of Osteoporosis when taking Arixtra ** :
How people recovered from Osteoporosis ** :
Top conditions involved for these people * :
- Breast cancer (2 people, 66.67%)
- Pain (2 people, 66.67%)
- Nausea (2 people, 66.67%)
- Metastases to bone (2 people, 66.67%)
Top co-used drugs for these people * :
- Morphine sulfate (2 people, 66.67%)
- Dyazide (2 people, 66.67%)
- Coumadin (2 people, 66.67%)
- Augmentan oral (2 people, 66.67%)
- Ibuprofen (2 people, 66.67%)
* 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 Osteoporosis while taking Arixtra?
Get connected! Join a mobile support group:
- support group for people who take Arixtra and have Osteoporosis
- support group for people who take Arixtra
- support group for people who have Osteoporosis
Comments from related studies:
From this study (1 month ago):
My celiac panel was very abnormal except for IGA which was normal. However I do not have GI symptoms. I have dizziness and light- headed ness. When I eliminated topamax the symptoms resolved. I wonder if topamax caused the blood work abnormality? I have taken it for 10 years?
From this study (4 months ago):
I have severe nausea, dizziness,headache, incontinence when taking Fondapariaux Sodium and Aritra have light headness, somnolence. I need to be on a anticoagulant because of stents just placed 6 months ago.
From this study (5 months ago):
I had a dvt and pe within 4 months of a previous one. I was on warfarin and within therapeutic range when I had my last pe. I was put on Arixtra and almost immediately I gained about 20 pounds around my waist. My waist size went from 32 inches to 36 inches within a matter of a few months. I have tried exercise and dieting to no avail. I also have asthma and with the lung damage from numerous PE's it is difficult to do strenuous workouts.
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On eHealthMe, Arixtra (fondaparinux sodium) is often used for deep venous thrombosis. Find out below the conditions Arixtra is used for, how effective it is, and any alternative drugs that you can use to treat those same conditions.
What is Arixtra used for and how effective is it:
Other drugs that are used to treat the same conditions:
Could it be a symptom from a condition:
Drugs in real world that are associated with:
Could your condition cause it?
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.
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