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Review: could Prolia cause Arthritis - osteoarthritis (Osteoarthritis)?

Summary: Arthritis - osteoarthritis is found among people who take Prolia, especially for people who are female, 60+ old, have been taking the drug for < 1 month, also take medication Vitamin d, and have Osteoporosis post-menopausal.

We study 5,805 people who have side effects while taking Prolia from FDA and social media. Among them, 20 have Arthritis - osteoarthritis. Find out below who they are, when they have Arthritis - osteoarthritis and more.

You are not alone: join a support group for people who take Prolia and have Arthritis - osteoarthritis >>>

 

Prolia

Prolia has active ingredients of denosumab. It is often used in osteoporosis. (latest outcomes from 5,841 Prolia users)

Arthritis - osteoarthritis

Arthritis - osteoarthritis (joint disease caused by cartilage loss in a joint) has been reported by people with osteoporosis, osteopenia, rheumatoid arthritis, high blood pressure, pain. (latest reports from 33,267 Arthritis - osteoarthritis patients)

On Mar, 2, 2015: 5,805 people reported to have side effects when taking Prolia. Among them, 20 people (0.34%) have Arthritis - Osteoarthritis.

Trend of Arthritis - osteoarthritis in Prolia reports

Time on Prolia when people have Arthritis - osteoarthritis * :

< 1 month1 - 6 months6 - 12 months1 - 2 years2 - 5 years5 - 10 years10+ years
Arthritis - osteoarthritis40.00%20.00%20.00%0.00%20.00%0.00%0.00%

Age of people who have Arthritis - osteoarthritis when taking Prolia * :

0-12-910-1920-2930-3940-4950-5960+
Arthritis - osteoarthritis0.00%0.00%0.00%0.00%0.00%0.00%0.00%100.00%

Severity of Arthritis - osteoarthritis when taking Prolia ** :

leastmoderateseveremost severe
Arthritis - osteoarthritis0.00%0.00%100.00%0.00%

How people recovered from Arthritis - osteoarthritis ** :

while on the drugafter off the drugnot yet
Arthritis - osteoarthritis0.00%0.00%100.00%

Top conditions involved for these people * :

  1. Osteoporosis postmenopausal (13 people, 65.00%)
  2. Osteoporosis (8 people, 40.00%)
  3. Glaucoma (5 people, 25.00%)
  4. Senile osteoporosis (5 people, 25.00%)
  5. Hypothyroidism (5 people, 25.00%)

Top co-used drugs for these people * :

  1. Vitamin d (8 people, 40.00%)
  2. Synthroid (6 people, 30.00%)
  3. Aspirin (6 people, 30.00%)
  4. Catapres (5 people, 25.00%)
  5. Antivert (5 people, 25.00%)

* 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.

Get connected: join our support group of prolia and arthritis - osteoarthritis on

Do you have Arthritis - Osteoarthritis while taking Prolia?

 

 

 

You are not alone! Join a mobile support group on :
- support group for people who take Prolia and have Arthritis - Osteoarthritis
- support group for people who take Prolia
- support group for people who have Arthritis - Osteoarthritis

Drugs in real world that are associated with:

Could your condition cause:

Recent related drug studies (Check your drugs):

Recent Prolia related drug comparison:

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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