Actonel and Post procedural haemorrhage - a phase IV clinical study of FDA data

Summary:

Post procedural haemorrhage is reported as a side effect among people who take Actonel (risedronate sodium), especially for people who are female, 60+ old, have been taking the drug for 1 - 2 years also take Fosamax, and have Rheumatoid arthritis.

The phase IV clinical study analyzes which people have Post procedural haemorrhage when taking Actonel. It is created by eHealthMe based on reports of 28,929 people who have side effects when taking Actonel from the FDA, and is updated regularly.

What is Actonel?

Actonel has active ingredients of risedronate sodium. It is often used in osteoporosis. eHealthMe is studying from 29,369 Actonel users. Check the latest studies of Actonel.

What is Post procedural haemorrhage?

Post procedural haemorrhage (post procedural bleeding) is found to be associated with 665 drugs and 854 conditions by eHealthMe. Check the latest studies of Post procedural haemorrhage.



On Jul, 15, 2026

28,929 people reported to have side effects when taking Actonel.
Among them, 38 people (0.13%) have Post procedural haemorrhage.

Could Actonel cause Post procedural haemorrhage?

Among these 38 people:

How long have people been on Actonel when they have Post procedural haemorrhage? *

  • < 1 month: 0.0 %
  • 1 - 6 months: 0.0 %
  • 6 - 12 months: 16.67 %
  • 1 - 2 years: 41.67 %
  • 2 - 5 years: 16.67 %
  • 5 - 10 years: 16.67 %
  • 10+ years: 8.33 %

What is the gender of people who have Post procedural haemorrhage when taking Actonel? *

  • female: 89.47 %
  • male: 10.53 %

What is the age of people who have Post procedural haemorrhage when taking Actonel? *

  • 0-1: 0.0 %
  • 2-9: 0.0 %
  • 10-19: 0.0 %
  • 20-29: 0.0 %
  • 30-39: 0.0 %
  • 40-49: 3.33 %
  • 50-59: 13.33 %
  • 60+: 83.33 %

What are other drugs people take besides Actonel? *

  1. Fosamax: 17 people, 44.74%
  2. Lipitor: 7 people, 18.42%
  3. Omeprazole: 6 people, 15.79%
  4. Levaquin: 5 people, 13.16%
  5. Ambien: 5 people, 13.16%
  6. Aspirin: 5 people, 13.16%
  7. Premarin: 5 people, 13.16%
  8. Advair Hfa: 4 people, 10.53%
  9. Boniva: 4 people, 10.53%
  10. Colace: 4 people, 10.53%

What are other side effects people have besides Post procedural haemorrhage? *

  1. Femur Fracture: 20 people, 52.63%
  2. Osteoarthritis (a joint disease caused by cartilage loss in a joint): 12 people, 31.58%
  3. Pain In Extremity: 12 people, 31.58%
  4. Fall: 12 people, 31.58%
  5. High Blood Pressure: 11 people, 28.95%
  6. Stress And Anxiety: 11 people, 28.95%
  7. Pain: 11 people, 28.95%
  8. Depression: 10 people, 26.32%
  9. Anaemia Postoperative: 10 people, 26.32%
  10. Urinary Tract Infection: 9 people, 23.68%

What are the existing conditions these people have? *

  1. Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 7 people, 18.42%
  2. High Blood Pressure: 2 people, 5.26%
  3. Chronic Lymphocytic Leukaemia (cancer in which the bone marrow makes too many lymphocytes (a type of white blood cell)): 2 people, 5.26%
  4. Cerebral Infarction (less blood supply to brain resulting tissue damage): 2 people, 5.26%
  5. Bone Density Decreased: 2 people, 5.26%
  6. Back Pain: 2 people, 5.26%
  7. Systemic Lupus Erythematosus (an autoimmune disease, which means the body's immune system mistakenly, attacks healthy tissue): 1 person, 2.63%
  8. Neuralgia (pain in one or more nerves): 1 person, 2.63%
  9. Nausea (feeling of having an urge to vomit): 1 person, 2.63%
  10. Hypertonic Bladder (bladder-storage function that causes a sudden urge to urinate): 1 person, 2.63%

* Approximation only. Some reports may have incomplete information.

Do you take Actonel and have Post procedural haemorrhage?

- Check whether Post procedural haemorrhage is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously



Related studies:

Effectiveness of, long term effects of, and alternative drugs to Actonel:

Post procedural haemorrhage treatments and more:

How severe was Post procedural haemorrhage and when was it recovered:

Expand to all the drugs that have ingredients of risedronate sodium:

Sub-studies by gender and age:

Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Browse all side effects of Actonel:

a b c d e f g h i j k l m n o p q r s t u v w x y z

Browse all the drugs that are associated with Post procedural haemorrhage:

Browse all the conditions that are associated with Post procedural haemorrhage:

Related publications that referenced our studies


How the study uses the data?

The study uses data from the FDA. It is based on risedronate sodium (the active ingredients of Actonel) and Actonel (the brand name). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Dosage of drugs is not considered in the study.

How to use the study?

DO NOT STOP MEDICATIONS without first consulting your doctor. If there are any serious or long term adverse effects discovered in the study, discuss the study with your doctor to ensure that proper medication management will be in place if applicable.

Who is eHealthMe?

With medical big data and proven AI/ML algorithms, eHealthMe provides a platform for everyone to run phase IV clinical trials. We study millions of patients and 5,000 more each day. Results of our real-world drug study have been referenced on 800+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and Nature. Our analysis results are available to researchers, health care professionals, patients (testimonials), and software developers (open API).

WARNING, DISCLAIMER, USE FOR PUBLICATION

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. Our phase IV clinical studies alone cannot establish cause-effect relationship. 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.

If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.



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